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Transparent Liquid Soap

Abstract: Transparent liquid soap transparent cleansing liquid composition containing, in a physiologically acceptable aqueous medium: - at least a soap, - at least one foaming surfactant, - at least an organic neutralizing agent present in a molar ratio between soap and said organic neutralizing agent of at least 1:1.75, and - at least a viscosity enhancing polymer comprising at least a hydroxy(C1-C6)alkyl(C1-C6)alkyl cellulose, wherein the organic neutralizing agent imparts a pH ranging from 8 to 9, preferably from 8 to 8.5, to the composition. rocess for cleansing keratin materials, which consists in applying to the said keratin materials a composition according to the invention.

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Patent Information

Application #
Filing Date
31 October 2014
Publication Number
19/2016
Publication Type
INA
Invention Field
CHEMICAL
Status
Email
Parent Application

Applicants

L'OREAL
14 RUE ROYALE, F-75008 PARIS FRANCE

Inventors

1. PATTANAIK, SHOIBAL
L'ORÉAL INDIA PVT LTD RESEARCH & INNOVATION UNIVERSAL MAJESTIC, GHATKOPAR - MANKHURD LINK ROAD, CHEMBUR MUMBAI MAHARASHTRA 400071 INDIA
2. AGRAWAL, TANU
L'ORÉAL INDIA PVT LTD RESEARCH & INNOVATION UNIVERSAL MAJESTIC, GHATKOPAR - MANKHURD LINK ROAD, CHEMBUR MUMBAI MAHARASHTRA 400071 INDIA

Specification

"Transparent liquid soap"
The present invention relates to a transparent liquid soap based personal care
and/or cleansing foaming composition which provides skin freshness throughout the day,
moisturization, skin smoothness at the moment of deposit and all day, and skin softness.
The product also gives quick abundant foam.
We know from document WO 2007/112852 a clear cleansing composition that
provides moisturization and comprises an anionic surfactant and another surfactant chosen
among amphoteric surfactant, nonionic surfactant or a mixture thereof and additionally
comprising humectants.
Documents WO2004/058212 and WO2004/100862 disclose oil-in-water
formulations both comprising silicone components in the oily phase and polyols or
hydroxy acids in the aqueous phase.
Document EP 1 100 459 Bl discloses a single-phase foaming oil formulation
comprising at least one nonionic surfactant, an anionic or zwitterionic surfactant, an oil
component and at least one alkyl phosphate component.
Document US 5,030,374 discloses a clear transparent gel facial cleanser
formulation having a neutral pH, which is non-foaming and characterized by rapid
rinseability consisting essentially of mild nonionic detergent and wound cleanser,
moisturizer/humectant, gelling agent, viscosity stabilizer, pH adjuster, substantive
emollient, preservative/bacterial inhibitor, solubilizer, masking agent, and deionized water.
Moreover JP 2008-137904 describes a liquid skin detergent composition
comprising (A) 2-30 mass% of a fatty acid salt, (B) 0.1-3 mass% of a nonionic water-
soluble polymer compound or anionic water-soluble polymer compound and (C) 0.3-5
mass% of a water-soluble silicone compound.
None of the disclosed transparent compositions achieves completely satisfying
quality foaming properties while giving mildness and moisturizing to the skin
simultaneously.
In addition, the visual appearance of product has impact on consumer's
perception. For example, a clear and transparent facial cleanser is mostly related to
freshness, mildness. Duritv. cooling, cleanliness etc. bv consumers. TransDarent Droducts

when packed in a transparent packaging gives an opportunity for consumers to see the
entire product.
Consequently, there is a need for a transparent and stable liquid cleansing
composition. Advantageously, this transparent and stable liquid cleansing composition
presents good lathering, oil control properties suitable for the use of face and/or body wash
comprising a minimal amount of surfactant. Advantageously, the needed composition is
also mild, moisturizing, respects skin and is environment friendly and biodegradable.
In the present invention, a stable composition means stable at 4°C during 1
month, preferably during 2 months.
The inventors have demonstrated that a combination of:
- at least a soap,
- at least one foaming surfactant,
- at least an organic neutralizing agent present in a molar ratio between soap
and said organic neutralizing agent of at least 1:1.75, preferably of at least
1:1.8, and
- at least a viscosity enhancing polymer comprising at least a
hydroxy(C1-C6)alkyl(C1-C6)alkyl cellulose,
makes it possible to provide a transparent and stable cleansing composition that
advantageously gives creamy lathering, moisturizing skin feel and is mild.
One object of the present invention is thus a transparent cleansing liquid
composition containing, in a physiologically acceptable aqueous medium:
- at least a soap,
- at least one foaming surfactant,
- at least an organic neutralizing agent present in a molar ratio between soap
and said organic neutralizing agent of at least 1:1.75, preferably of at least
1:1.8, and
- at least a viscosity enhancing polymer comprising at least a
hydroxy(C1-C6)alkyl(C1-C6)alkyl cellulose,
wherein said composition has a pH ranging from 8 to 9, preferably from 8 to
8.5.

The cleansing composition according to the invention may be used as facial
cleanser, for example as makeup removal as well as hand and body cleanser.
According to another aspect, a subject of the present invention is also a process
for cleansing keratin materials, which consists in applying to said keratin materials a
composition according to the present invention, eventually with water, followed by rinsing
with water to eliminate foam and dirt. The composition may be applied directly on wet
keratin materials, or alternatively mixed with water and then applied on keratin materials.
For the purposes of the present invention, the expression "physiologically
acceptable medium" means a medium that is suitable for application of a composition
according to the invention on keratinous material, such as skin.
A physiologically acceptable medium is preferably a cosmetically or
dermatologically acceptable medium, that is to say a medium which is devoid of
unpleasant odor or appearance and which is entirely compatible with the topical
administration route.
Such a medium is in particular considered as physiologically acceptable when
it does not cause the user any unacceptable stinging, tautness or redness.
For the purpose of the present invention, the term "liquid" means in liquid
form, for example the composition flows under its own weight at ambient temperature (25
°C) and atmospheric pressure in less than 5 seconds.
Viscosity measurement
In the framework of the present invention, the viscosity measurements are
performed at 25 ° C and atmospheric pressure using a Rheomat RM180® apparatus.
The sample is brought at the temperature of 25 °C ± 0.5 °C. The viscosity is
measured using mobile 3 attachment to Rheomat RM180® at a rotation speed of 200
(fixed) after rotation of the measuring instrument for 10 minutes. The corresponding value
in UD (unit deflection) is converted to Pa.s.
Transparency
The composition accordina to the invention is transparent. The transparencv of

at 25 °C and atmospheric pressure, using a Shimadzu UV-1800 spectrometer through a
quartz cuvette of 3.5 mL and pathlength of 10 mm. According to the invention, the
composition is transparent when the transmittance value is superior to 90% in this
wavelength range.
The composition according to the invention contains surfactant(s) and soap(s)
that gives the composition its foaming nature.
The foaming cleansing composition according to the invention contains at least
a soap and at least one foaming surfactant.
According to another particular embodiment, the foaming surfactant is present
in the composition in an amount ranging from 0.5 to 10% by weight, in particular from 2 to
8% by weight, more particularly from 3 to 6% by weight relative to the total weight of the
composition.
Foaming surfactants are detergents and differ from emulsifiers in the value of
their HLB (Hydrophilic-Lipophilic Balance), the HLB being the ratio of the hydrophilic
part to the lipophilic part in the molecule. The term "HLB" is well known to a person
skilled in the art and is described, for example, in "The HLB system. A time-saving guide
to Emulsifier Selection" (published by ICI Americas Inc., 1984). For emulsifiers, the HLB
generally ranges from 3 to 8 for the preparation of W/O emulsions and from 8 to 18 for the
preparation of O/W emulsions, whereas foaming surfactants generally have an HLB of
greater than 20.
According to still another particular embodiment, the foaming surfactant at
least contains an anionic surfactant.
According to a further particular embodiment, the foaming surfactant further
contains a cationic surfactant. Said cationic surfactant may be present in the composition in
an amount of less than 2% by weight relative to the total weight of the composition. More
particularly, such a cationic surfactant may be present in an amount ranging from 0.001 to
0.5% and more preferably from 0.01 to 0.1% by weight relative to the total weight of the
composition.
As far as soap is concerned the amount to be taken in consideration for the
calculation of the soap amount is the total fatty acid content without the neutralizing agent.

SOAP
The soap used in the framework of the present invention is an organic soap of
fatty acid from 10 to 22 carbon atoms, more preferably from 12 to 18 carbon atoms and
most preferably from 12 to 14 carbon atoms.
The fatty acid can in particular be selected among the the caproic acid, the
capric acid, the caprylic acid, the oleic acid, the linoleic acid, lauric acid, the myristic acid,
the stearic acid, the palmitic acid and mixtures thereof.
The neutralizing agent may be selected from aminoalcohols such as
ethanolamine, amino sugars, amino acids, and their alkali salts. Most preferred neutralizing
agent is triethanolamine.
The neutralization of soap may be achieved by having a molar ratio between
fatty acid to neutralizing agent of at least 1:1.75, preferably of at least 1:1.8.
According to another embodiment, the molar ratio between fatty acid to
neutralizing agent ranges from 1:1.75 to 1:3, in particular from 1:1.8 to 1:2.5.
Soap content in the composition may for example range from 2 to 7% by
weight, more preferably from 3 to 6% by weight and most preferably from 4 to 5% by
weight, relative to the total weight of the composition.
FOAMING SURFACTANT
The foaming cleansing composition according to the invention comprises one
or more surfactants.
The surfactants may be selected from anionic, amphoteric (or zwitterionic),
nonionic and/or cationic foaming surfactants, and mixtures thereof.
Anionic surfactants
The composition according to the invention may also comprise one or more
anionic surfactants.
The term anionic surfactant means a surfactant having only anionic groups as
ionic or ionizable groups.
In the present description, an entity is qualified as "anionic" when it has at least

under the conditions of use of the composition of the invention (medium, pH, for example)
and containing no cationic charge.
The anionic surfactants may be sulfate(s) or sulfonate(s) which have at least
one sulfate group (-OSO3H or -OSO3"), and/or a sulfonate group (-SO3H or -SO3), or else
carboxylic or carboxylate surfactants having at least one carboxylic acid group (-COOH or
-COO").
It is understood that the anionic carboxylate surfactants may include one or
more sulfate or sulfonate groups; sulfonate anionic surfactants may optionally further
comprise one or more sulfate or carboxylate groups; and sulfate anionic surfactants may
optionally further comprise one or more carboxylate or sulfonate groups.
Anionic surfactants which may be used include alkyl sulfates, alkyl ether
sulfates, alkylamido ether sulfates, alkylaryl polyether sulfates, monoglyceride sulfates,
alkyl sulfonates or alpha olefin sulfonates, alkylamide sulfonates, alkylarylsulfonates,
paraffin sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylamide
sulfosuccinates, alkyl sulfoacetates, acylsarcosinates, acylglutamates, alkyl
sulphosuccinamates, acylisethionates and N-acyl taurates, salts of alkyl monoesters and
polyglycosidepolycarboxylic acids, acyl lactylates, N-acyl glycinates, salts of D-
galactoside-uronic acids, salts of alkyl ether carboxylic acids, alkyl aryl ether carboxylic
acid salts, salts of alkyl amidoether carboxylic acids, sulfoacetates, sulfolaurates, and the
corresponding non-salt forms all of these compounds, the alkyl and acyl groups of all these
compounds containing from 6 to 40 carbon atoms, especially 14 to 30 carbon atoms, more
preferably from 16 to 22 carbon atoms; and aryl means phenyl group. These compounds
may be ethoxylated and then preferably comprise from 1 to 50 ethylene oxide units.
Ethylene polyoxyalkylenated (C6-C24) (amido) ether carboxylic acids and salts
thereof may also be cited, in particular those comprising from 2 to 50 alkylene oxide
groups, in particular, such as sold by the company KAO under the names AKYPO.
The more preferred alkyl (C6-C24) (amido) ether carboxylic acids correspond to
the following formula:
R1-(OC2H4)n—OCH2COOA (1)
wherein:
- R1 represents a radical or a mixture of linear or branched alkyl or alkenyl in C8-C.22. a

radical linear or branched alkenyl in C9-C21; preferably Rl being an alkyl radical having 8
to 20 carbon atoms, preferably from 8 to 18 carbon atoms and aryl preferably denoting
phenyl,
- n is an integer or decimal number (average value) which may vary from 2 to 24 and
preferably 2 to 10,
- A denotes H, ammonium, Na, K, Li, Mg or monoethanolamine or triethanolamine.
It is also possible to use mixtures of compounds of formula (1), in particular mixtures in
which the Rl groups differ.
Polyoxyalkylenated (C6-C24) (amido) ether carboxylic acids preferably used in
the present invention are selected from those of formula (1) wherein:
- Rl denotes a radical or a mixture of (C12-C14)alkyl radicals, cocoyl, oleyl, a
nonyl or octylphenyl radical,
- A denotes hydrogen or sodium, and
- n is from 2 to 20 and preferably 2 to 10.
Polyoxy(C6-C24)alkylenated ether carboxylic acids and their salts are
preferably used, and also polyoxyalkylenated (C6-C24)alkylamido ether carboxylic acids
and salts thereof; in particular those having from 2 to 15 alkylene oxide groups.
Even more preferably, one can use the compounds of formula (I) wherein R is
a C12 alkyl radical, A denotes hydrogen or sodium and n is from 2 to 10.
Salts are especially selected from alkali metal salts, especially sodium,
ammonium salts, amine salts, amino alcohol such as triethanolamine or
monoethanolamine, and magnesium salts.
Preferably, the anionic surfactants are chosen from, alone or as a mixture:
- (C6-C24)alkylsulfates, especially in C12-C20,
- (C6-C24)alkyl ether sulfates, especially in C12-C20, preferably containing from
2 to 20 ethylene oxide units,
(C6-C24)alkylsulfosuccinates, especially in C12-C20, including
laurylsulfosuccinates,
- (C6-C24)alkyl ether sulfosuccinates, especially in C12-C20,
(C6-C24)acyl sarcosinates, especially in C12-C20, including

- (C6-C24)alkyl ether carboxylates, preferably (C12-C20)alkyl ether carboxylates,
- (C6-C24)acyl isethionates, preferably (C12-C18)acyl isethionates,
- polybxyalkylenated (C6-C24)alkyl (amido) ether carboxylic acids and salts
thereof, in particular those comprising from 2 to 50 alkylene oxide groups, especially
ethylene,
- (C6-C24)acylglutamates, especially in C12-C20,
- (C6-C24)acylglycinates, especially in C12-C20,
particularly in the form of alkali or alkaline earth metal, ammonium, amine or
aminoalcohol.
More Preferably, the anionic surfactant is chosen from (C6-C24)alkyl sulfates,
(C6-C24)alkyl ether sulfates such as sodium lauryl ether sulfate, isethionates, amino acids,
in particular glycinates, such as sodium N-cocoyl glycinate, their alkali salts, and mixtures
thereof.
Amphoteric and zwitterionic foaming surfactants
The composition according to the invention may also comprise one or more
amphoteric surfactants.
The amphoteric surfactants that may be used in the invention may be optionally
quatemized secondary or tertiary aliphatic amine derivatives, in which the aliphatic group
is a linear or branched chain comprising from 8 to 22 carbon atoms, said amine derivatives
containing at least one anionic group, for instance a carboxylate, sulfonate, sulfate,
phosphate or phosphonate group.
Mention may be made in particular of (C8-C20)alkylbetaines, sulfobetaines,
(C8-C2o)alkylsulfobetaines, (C8-C20)alkylamido(C1-C6)alkylbetaines, such as
cocamidopropylbetaine, and (C8-C20)alkylamido(C1-C6)aIkylsulfobetames, and mixtures
thereof.
Among the optionally quatemized secondary or tertiary aliphatic amine
derivatives that may be used, mention may also be made of the products of respective
structures (A1) and (A2) below:
(A1) Ra-CON(Z)CH2-(CH2)m-N+(Rb)(Rc)(CH2COO")

Ra represents a (C10-C30)alkyl or alkenyl group derived from an acid
Ra-COOH preferably present in hydrolyzed coconut oil, a heptyl group, a nonyl group or
an undecyl group,
Rb represents a p-hydroxyethyl group,
Re represents a carboxymethyl group,
m is equal to 0, 1 or 2,
Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group;
(A2) Ra.-CON(Z)CH2-CH2)m'-N(B)(B')
in which:
B represents -CH2CH2OX', with X' representing -CH2-COOH, CH2-COOZ',
-CH2CH2-COOH, -CH2CH2-COOZ', or a hydrogen atom,
B' represents -(CH2)Z-Y', with z = 1 or 2, and Y' representing -COOH, -COOZ',
-CH2-CHOH-SO3H or -CH2-CHOH-SO3Z',
m' is equal to 0,1 or 2,
Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group,
Z' represents an ion resulting from an alkali or alkaline-earth metal, such as
sodium, potassium or magnesium; an ammonium ion; or an ion resulting from an organic
amine and in particular from an amino alcohol, such as monoethanolamine, diethanolamine
and triethanolamine, monoisopropanolamine, diisopropanolamine or triisopropanolamine,
2-amino-2-methyl-l-propanol, 2-amino-2-methyl-l,3-propanediol and
tris(hydroxymethyl)aminomethane,
Ra' represents a (C10-C30)allcyl or alkenyl group of an acid Ra COOH preferably
present in hydrolyzed linseed oil or coconut oil, an alkyl group, in particular a C17 alkyl
group, and its iso form, or an unsaturated C17 group.
The compounds corresponding to formula (A2) are preferred.
Among the compounds corresponding to formula (A2) in which X' represents
an hydrogen atom, mention may be made of compounds classified in the CTFA dictionary,
under the names sodium cocoamphoacetate, sodium lauroamphoacetate, sodium
caproamphoacetate and sodium capryloamphoacetate.

Compounds corresponding to formula (A2) may be
(C8-C20)alkylamphoacetates and (C8-C2o)alkylamphodiacetates and mixtures thereof.
Other compounds corresponding to formula (A2) are disodium
cocoamphodiacetate, disodium lauroamphodiacetate, disodium caproamphodiacetate,
disodium capryloamphodiacetate, disodium cocoamphodipropionate, disodium
lauroamphodipropionate, disodium caproamphodipropionate, disodium
capryloamphodipropionate, lauroamphodipropionic acid and cocoamphodipropionic acid.
Examples that may be mentioned include the cocoamphodiacetate sold by the
company Rhodia under the trade name Miranol® C2M Concentrate, the sodium
cocoamphoacetate sold under the trade name Miranol Ultra C 32 and the product sold by
the company Chimex under the trade name Chimexane HA.
Use may also be made of the compounds of formula (A3):
(A3) Ra"-NH-CH(Y")-(CH2)n-C(O)-NH-(CH2)n'-N(Rd)(R£)
in which:
- Ra" represents a (C10-C30)alkyl or alkenyl group of an acid Ra»-C(O)OH
preferably present in hydrolysed linseed oil or coconut oil;
- Y" represents the group -C(O)0H, -C(0)OZ", -CH2-CH(OH)-S03H or the
group -CH2-CH(OH)-SO3-Z", with Z" representing a cationic counterion resulting from
an alkali metal or alkaline-earth metal, such as sodium, an ammonium ion or an ion
resulting from an organic amine;
- Rd and Re represent, independently of each other, a (C1-C4)alkyl or
hydroxyalkyl radical; and
- n and n' denote, independently of each other, an integer ranging from 1 to 3.
Among the compounds corresponding to formula (A3), mention may in
particular be made of the compound classified in the CTFA dictionary under the name
sodium diethylaminopropyl cocoaspartamide, such as the one sold by the company Chimex
under the name Chimexane HB.
Preferably, the amphoteric surfactants are chosen from (C8-C2o)alkylbetaines,
(C8-C20)alkylamido(C1-C6)alkylbetaines, (C8-C20)alkylamphoacetates and

Nonionic foaming surfactant
The composition may comprise one or more nonionic alkylpolyglycoside
surfactants, especially represented by formula (I):
R1O-(R2O),-(G)v
wherein:
- R1 represents a linear or branched alkyl or alkenyl radical having 6 to 24
carbon atoms, especially 8 to 18 carbon atoms, or an alkylphenyl radical whose linear or
branched alkyl radical comprises from 6 to 24 carbon atoms, especially 8 to 18 carbon
atoms,
- R2 represents an alkylene radical having 2 to 4 carbon atoms,
- G is a sugar unit containing 5 to 6 carbon atoms,
-1 is a value ranging from 0 to 10, preferably from 0 to 4,
- v is a value ranging from 1 to 15, preferably from 1 to 4.
Preferably, the alkylpolyglycoside surfactants are compounds of formula (I)
described above wherein:
- R1 denotes a linear or branched saturated or unsaturated alkyl radical having 8
to 18 carbon atoms,
- R2 represents an alkylene radical having 2 to 4 carbon atoms,
-1 is a value ranging from 0 to 3, preferably equal to 0,
- G denotes glucose, fructose or galactose, preferably glucose,
- the degree of polymerization, ie the value of v can range from 1 to 15,
preferably from 1 to 4; the average degree of polymerization is more particularly between
1 and 2.
Glycosidic linkages between the sugar units are generally 1-6 or 1-4, preferably
1-4.
Preferably, the alkylpolyglycoside surfactant is an alkylpolyglucoside
surfactant, even more preferably an C8-C16 alkylpolyglucosides, and particularly
preferably chosen among decylglucosides, caprylyl/capryl glucosides, laurylglucoside,

Among the commercial products, the following product may be cited: products
sold by COGNIS under the names PLANTAREN® (600 CS / U, 1200 and 2000) or
PLANTACARE® (818, 1200 and 2000); products sold by SEPPIC under the names
ORAMIX® CG 110 and ORAMIX® NS 10; products sold by BASF under the name
LUTENSOL GD 70 or products sold by the company CHEM Y under the name AG10 LK.
Preferably, C8-C16 alkylpolyglucosides is used, in particular chosen from
decylglucoside, caprylyl/capryl glucoside, laurylglucoside, cocoylglucoside,
caprylylglucoside, and mixtures thereof.
Cationic surfactant
The cosmetic composition according to the invention may also comprise one or
more cationic surfactants. They are advantageously chosen from optionally
polyoxyalkylenated primary, secondary or tertiary fatty amine salts, quaternary ammonium
salts, and mixtures thereof.
Mention may be made in particular of:
- quaternary ammonium salts having formula (la):

in which:
the groups R8 to R11, which may be identical or different, represent a linear or
branched aliphatic group containing from 1 to 30 carbon atoms, or an aromatic group such
as aryl or alkylaryl, at least one of the groups R8 to R11 containing from 8 to 30 carbon
atoms and preferably from 12 to 24 carbon atoms; it being possible for the aliphatic groups
to comprise heteroatoms such as, in particular, oxygen, nitrogen, sulfur or halogens; and
X" is an anion that could be chosen from the group consisting of halides,
phosphates, acetates, lactates, (C1-C4)alkyl sulfates, (C1-C4)alkylsulfonates and
(C1-C4)alkylarylsuIfonates.

The aliphatic groups are chosen, for example, from (C1-C30)alkyl,
(C1-C30)alkoxy, (C2-C6)poIyoxyalkylene, (C1-C30)alkylamide,
(C12-C22)alkyl(C2-C6)alkylamido, (C12-C22)alkyl acetate and hydroxy(C1-C30)alkyl groups.
Mention may be made of tetraalkylammonium halides, preferably chlorides,
such as dialkyldimethylammoniurn or alkyltrimethylammonium chlorides in which the
alkyl group comprises from 12 to 22 carbon atoms, particularly
behenyltrimethylammonium, distearyldimethylammonium, cetyltrimethylammonium, and
benzyldimethylstearylammonium chlorides.
Mention may also be made of palmitylamidopropyltrimethylammonium
halides, preferably chlorides, or stearamidopropyldimethyl(myristyl acetate)-ammomurn
halides, preferably chlorides, such as the product sold under the name Ceraphyl® 70 by the
company VAN DYK.
- imidazoline quaternary ammonium salts having formula (IIa):

in which :
R12 represents an alkenyl or alkyl group comprising from 8 to 30 carbon atoms,
for example fatty acid derivatives of tallow;
R13 represents a hydrogen atom, a (C1-C4)alkyl group or an alkenyl or alkyl
group comprising from 8 to 30 carbon atoms;
R14 represents a (C1-C4)alkyl group;
R15 represents a hydrogen atom or a (C1-C4)alkyl group;
X is an anion, preferably chosen from the group consisting of halides,
phosphates, acetates, lactates, (C1-C4)alkyl sulfates, (C1-C4)alkylsulfonates and
(C1-C4)alkylarylsulfonates;
R12 and R13 preferably denote a mixture of alkenyl or alkyl groups containing

methyl group, and R15 denotes a hydrogen atom. A product of this kind is sold for
example under the name Rewoquat® W 75 by the company Rewo.
- quaternary di- or triammonium salts having formula (IIIa):

in which:
R16 denotes an alkyl group containing from 16 to 30 carbon atoms, which is
optionally hydroxylated and/or interrupted with one or more oxygen atoms,
R17 represents a hydrogen atom or an alkyl group containing from 1 to 4 carbon
atoms or a group -(CH2)3-N+(R16a)(R17a)(R18a); wherein R16a, R17a, R18a, which may be
identical or different, are chosen from hydrogen and an alkyl group comprising from 1 to 4
carbon atoms
R18, R19, R20 and R21, which may be identical or different, are chosen from
hydrogen and an alkyl group comprising from 1 to 4 carbon atoms; and
X is an anion preferably chosen from the group consisting of halides, acetates,
phosphates, nitrates, (C1-C4)alkyl sulfates, (C1-C4)alkylsulfonates and
(C1-C4)alkylarylsulfonates, in particular methyl sulfate and ethyl sulfate.
Such compounds are, for example, Finquat CT-P, sold by the company Finetex
(Quatemium 89), and Finquat CT, sold by the company Finetex (Quatemium 75).
- quaternary ammonium salts containing one or more ester functions having the
following formula (IVa):


in which:
R22 is chosen from (C1-C6)alkyl groups and hydroxy(C1-C6)alkyl or
dihydroxy(Ci-C6)alkyl groups;
R23 is chosen from the group R26-C(=O)-; hydrocarbon-based linear or
branched, saturated or unsaturated C1-C22 groups R27; and a hydrogen atom;
R25 is chosen from the group R2g-C(=O)-; hydrocarbon-based linear or
branched, saturated or unsaturated C1-C6 groups R29; and a hydrogen atom;
R24, R26 and R28, which may be identical or different, are chosen from linear or
branched, saturated or unsaturated C7-C21 hydrocarbon-based groups;
r, s and t, which may be identical or different, are integers ranging from 2 to 6;
r1 and t1, which may be identical or different, are equal to 0 or 1;
r2 + rl = 2 r and tl +12 = 21;
y is an integer ranging from 1 to 10;
x and z, which may be identical or different, are integers ranging from 0 to 10;
the sum x + y + z is from 1 to 15,
X is an anion;
with the proviso that, when x is 0 then R23 denotes R27, and that when z is 0
then R25 denotes R29.
The alkyl groups R22 may be linear or branched, and more particularly linear.
Preferably, R22 denotes a methyl, ethyl, hydroxyethyl or dihydroxypropyl group, and more
particularly a methyl or ethyl group.
When R23 is an R27 hydrocarbon group, it may have from 12 to 22 carbon
atoms, or may have from 1 to 3 carbon atoms.
When R25 is an R29 hydrocarbon group, it preferably has 1 to 3 carbon atoms.
Advantageously, R24, R26 and R28, which are identical or different, are chosen
from linear or branched, saturated or unsaturated C11-C21 hydrocarbon groups, and more
particularly from linear or branched C11-C21 alkyl and alkenyl groups.
Preferably, x and z, which may be identical or different, are equal to 0 or 1.
Advantageously, y is equal to 1.
Advantageously, the sum x + y + z is from 1 to 10.

Preferably, r, s and t, which may be identical or different, are equal to 2 or 3,
and even more particularly are equal to 2.
The anion X- is preferably a halide, preferably chloride, bromide or iodide, a
(C1-C4)alkyl sulfate, (C1-C4)alkyl sulfonate or (C1-C4)alkylaryl sulfonate,
methanesulfonate, phosphate, nitrate, tosylate, an anion derived from an organic acid, such
as acetate or lactate, or any other anion that is compatible with the ammonium comprising
an ester function. The anion X is more particularly chloride, methyl sulfate or ethyl
sulfate.
Use is made more particularly, in the composition according to the invention,
of the ammonium salts having formula (IVa) in which:
- R22 denotes a methyl or ethyl group,
- x and y are equal to 1,
-z is equal to 0 or 1,
- r, s and t are equal to 2,

- R23 is chosen from the group R26-C(=O)-; methyl groups, ethyl groups or
hydrocarbon-based C14-C22 groups; and a hydrogen atom,
- R25 is chosen from the group R.28-C(=O)-; and a hydrogen atom,
- R24, R26 and R28, which may be identical or different, are chosen from linear
or branched, saturated or unsaturated C13-C17 hydrocarbon groups, and preferably from
linear or branched, saturated or unsaturated C13-C17 alkyl and alkenyl groups.
The hydrocarbon-based groups are advantageously linear.
Among the compounds of formula (IVa), examples that may be mentioned
include salts, in particular the chloride or methyl sulfate of
diacyloxyethyldimethylammonium, diacyloxyethylhydroxyethylmethylammonium,
monoacyloxyethyldihydroxyethylmethylammonium, triacyloxyethylmethylammonium or
monoacyloxyethylhydroxyethyldimethylammonium, and mixtures thereof. The acyl groups
preferably contain 14 to 18 carbon atoms and are obtained more particularly from a plant
oil, such as palm oil or sunflower oil. When the compound contains several acyl groups,
these groups may be identical or different.

These products are obtained, for example, by direct esterification of
triethanolamine, triisopropanolamine, alkyldiethanolamine or alkyldiisopropanolamine,
which are optionally oxyalkylenated, with fatty acids or with fatty acid mixtures of plant or
animal origin, or by transesterification of the methyl esters thereof. This esterification is
followed by a quatemization by means of an alkylating agent, such as an alkyl halide,
preferably methyl or ethyl halide, a dialkyl sulfate, preferably methyl or ethyl sulfate,
methyl methanesulfonate, methyl para-toluenesulfonate, glycol chlorohydrin or glycerol
chlorohydrin. Such compounds'are, for example, sold under the names Dehyquart® by the
company Henkel, Stepanquat® by the company Stepan, Noxamium® by the company
Ceca or Rewoquat® WE 18 by the company Rewo-Witco.
The composition according to the invention may contain, for example, a
mixture of quaternary ammonium monoester, diester and triester salts with a weight
majority of diester salts. Use may also be made of the ammonium salts containing at least
one ester function that are described in patents US-A-4 874 554 and US-A-4 137 180. Use
may also be made of behenoylhydroxypropyltrimethylammonium chloride, for example,
sold by the company Kao under the name Quartamin BTC 131.
Preferably, the ammonium salts containing at least one ester function contain
two ester functions.
Preferably, the cationic surfactants are chosen from the compounds of formula
(Ia) and the compounds of formula (IVa), preferably from cetyltrimethylammonium,
behenyltrimethylammonium, and dipalmitoylethylhydroxyethylmethylammonium salts,
and mixtures thereof, and more particularly from behenyltrimethylammonium chloride or
methosulfate, cetyltrimethylammonium chloride or methosulfate, and
dipalmitoylethylhydroxyethylammonium chloride or methosulfate, and mixtures thereof.
Even more preferentially, tire cationic surfactant is a behenyltrimethylammonium salt.
According to a preferred embodiment, the composition comprises at least one
anionic surfactant, preferably chosen from alkyl ether sulfate comprising 6 to 24 carbon
atoms, preferably 2 to 20 carbon atoms; amino acids, in particular glycinates; and mixtures

In a particular embodiment, the composition comprises at least one anionic
surfactant, preferably chosen from sodium lauryl ether sulfate (SLES), in particular SLES
1EO, such as the one sold under the name Galaxy LES 170 by Galaxy Surfactants;
glycinates, such as sodium cocoyl glycinate.
VISCOSITY ENHANCING POLYMER
The cleansing composition according to the invention comprises at least one
viscosity enhancing polymer comprising at least a
hydroxy(C1-C6)alkyl(C1-C6)alkylcellulose.According to one particular embodiment, the
viscosity enhancing polymer comprises at least a
hydroxy(C1-C4)alkyl(C1-C4)alkylcellulose.
The viscosity of the viscosity enhancing polymer may be measured according
to the here above described protocol for an aqueous solution comprising 2% by weight of
said polymer.
According to a particular embodiment, the viscosity of the viscosity enhancing
polymer, when present in an aqueous solution at a weight concentration of 2%, varies
between 75 000 and 140 000 mPa.s.
The cellulose ether that may be used in accordance with the invention can
especially be selected from hydroxymethylbutylcellulose, hydroxyethylmethylcellulose,
hydroxyethylbutylcellulose and hydroxypropylmethylcellulose (also known as HPMC) and
mixtures thereof.
More preferably, the hydroxy(C1-C6)alkyl(C1-C6)alkylcellulose that is suitable
for use in the invention is hydroxypropylmethylcellulose.
According to said particular embodiment, hydroxypropylmethylcellulose
presents a hydroxypropyl content ranging for example from 7 to 12% by weight with
respect to the total weight of hydroxypropylmethylcellulose, and presents a methoxy
content ranging for example from 20 to 24% by weight with respect to the total weight of
hydroxypropylmethylcellulose.
Hydroxypropylmethylcellulose is especially sold under the name Metolose™
by the company Shin-Etsu, and more specifically, for example, under the names
Metolose™ 60 SH 4000, Metolose™ 60 SH 50, Metolose™ 90 SH 100, Metolose™ 90

Metolose™ 60 SH 4000, and Metolose™ 60 SH 5, under the name Methocel™ by the
company The Dow Chemical Company, and more specifically, for example, under the
names Methocel™ E-3, Methocel™ E-6, Methocel™ E-50, Methocel™ E4M, Methocel™
F50, Methocel™ F4M, Methocel™ K100, Methocel™ K4M and Methocel™ K100M,
under the name Headcel™ by the company Shandong Head, and more specifically, for
example, under the names Headcel™ 60HD3, Headcel™ 60HD15, Headcel™ 60HD4000,
Headcel™ 65HD50, Headcel™ 75HD100, Headcel™ 75HD4000, Headcel™ 75HD15000
and Headcel™ 75HD100000, and under the name BENECEL K100M sold by Ashland.
Among said hydroxypropylmethylcellulose, one may particularly cite
BENECEL K100M sold by Ashland.
The viscosity enhancing polymer may be present in a cleansing composition
according to the present invention in an amount ranging from 0.2 to 6% by weight, in
particular from 0.5 to 5% by weight and more particularly from 0.8 to 1.2% by weight,
with respect to the total weight of the composition.
COMPOSITION
The composition according to the invention may present a viscosity, measured
according to the here above described protocol, ranging from ranging from 0.1 Pa.s to 3
Pa.s, in particular from 0.2 to 2 Pa.s, and more particularly from 0.3 to 1.3 Pa.s.
The composition according to the invention comprises an aqueous medium or
aqueous phase.
The composition may comprise an amount of water of at least 50% by weight,
preferably ranging from 50% to 95% by weight and better still from 60% to 90% by weight
relative to the total weight of the composition. According to a particular embodiment, the
composition according to the invention comprises less than 1% by weight of oily
component relative to the total weight of the composition. According to a particular
embodiment, the composition is free of oil.
The cleansing composition according to the invention may contain various
water-soluble additives, chosen from those conventionally used in skincare or makeup-
removing products, insofar as these additives and the amounts thereof do not impact
neither the transparency, nor the stability desired for the composition according to the

The cleansing composition in accordance with the present invention may thus
comprise the following additives: preserving agents; sequestrants (EDTA and salts
thereof); antioxidants; fragrances; active ingredients
The amounts of these various adjuvants are those conventionally used in the
field under consideration, for example from 0.01% to 20% of active material of the total
weight of the composition. These adjuvants and the amounts thereof should be such that
they do not modify the property desired for the composition of the invention.
The composition according to the invention may also optionally comprise one
or more polymers chosen from amphoteric polymers, cationic polymers, and mixtures
thereof.
The term "cationic polymer" means any polymer comprising cationic groups
and/or groups that can be ionized to cationic groups. Preferably, the cationic polymer is
hydrophilic or amphiphilic. The preferred cationic polymers are chosen from those that
contain units comprising primary, secondary, tertiary and/or quaternary amine groups that
may either form part of the main polymer chain or may be bome by a side substituent
directly connected thereto.
The cationic polymers that may be used preferably have a weight-average
molar mass (Mw) of between 500 and 5*106 approximately and preferably between 103
and 3x106 approximately.
Among the cationic polymers, mention may be made more particularly of:
(polyquaternium 7 sold under Merquat 7SPR as present in the examples to
place in the following list, please) comment [RD1]:Ok, deja present au point (7)fin page 25
(1) homopolymers or copolymers derived from acrylic or methacrylic esters or
amides and comprising at least one of the units of the following formulae:


in which:
- R3, which may be identical or different, denote a hydrogen atom or a CH3
radical;
- A, which may be identical or different, represent a linear or branched divalent
alkyl group of 1 to 6 carbon atoms, preferably 2 or 3 carbon atoms, or a hydroxyalkyl
group of 1 to 4 carbon atoms;
- R4, R5 and R6, which may be identical or different, represent an alkyl group
containing from 1 to 18 carbon atoms or a benzyl radical, preferably an alkyl group
containing from 1 to 6 carbon atoms;
- R1 and R2, which may be identical or different, represent a hydrogen atom or
an alkyl group containing from 1 to 6 carbon atoms, preferably methyl or ethyl;
- X denotes an anion derived from a mineral or organic acid, such as a
methosulfate anion or a halide such as chloride or bromide.
The copolymers of family (1) may also contain one or more units derived from
comonomers that may be selected from the family of acrylamides, methacrylamides,
diacetone acrylamides, acrylamides and methacrylamides substituted on the nitrogen with
(C1-C4)alkyl, acrylic or methacrylic acids or esters thereof, vinyllactams such as
vinylpyrrolidone or vinylcaprolactam, and vinyl esters.
Among these copolymers of family (1), mention may be made of;
- copolymers of acrylamide and of dimethylaminoethyl methacrylate
quaternized with dimethyl sulfate or with a dimethyl halide, such as the product sold under
the name Hercofloc by the company Hercules,

- copolymers of acrylamide and of methacryloyloxyethyltrimethylammonium
chloride, such as those sold under the name Bina Quat P 100 by the company Ciba Geigy,
- copolymers of acrylamide and of methacryloyloxyethyltrimethylammonium
methosulfate, such as the product sold under the name Reten by the company Hercules,
-quaternized or non-quaternized vinylpyrrolidone/dialkylaminoalkyl acrylate
or methacrylate copolymers, such as the products sold under the name Gafquat by the
company ISP, for instance Gafquat 734 or Gafquat 755, or alternatively the products
known as Copolymer 845, 958 and 937. These polymers are described in detail in French
patents 2 077 143 and 2 393 573,
dimethylaminoethyl memacrylate/vinylcaprolactam/vinylpyrrolidone
terpolymers, such as the product sold under the name Gaffix VC 713 by the company ISP,
- vinylpyrrolidone/methacrylamidopropyldimethylamine copolymers, such as
those sold under the name Styleze CC 10 by ISP,
quaternized vinylpyrrolidone/dimethylaminopropylmethacrylamide
copolymers such as the product sold under the name Gafquat HS 100 by the company ISP,
- preferably crosslinked polymers of
methacryloyloxy(C1-C4)alkyltri(C1.C4)alkylammonium salts, such as the polymers
obtained by homopolymerization of dimethylaminoethyl methacrylate quaternized with
methyl chloride, or by copolymerization of acrylamide with dimethylaminoethyl
methacrylate quaternized with methyl chloride, the homopolymerization or
copolymerization being followed by crosslinking with an olefinically unsaturated
compound, more particularly methylenebisacrylamide. A crosslinked
acrylamide/methacryloyloxyethyltrimethylammonium chloride copolymer (20/80 by
weight) in the form of a dispersion containing 50% by weight of the said copolymer in
mineral oil may be used more particularly. This dispersion is sold under the name
Salcare® SC 92 by the company Ciba. A crosslinked
methacryloyloxyethyltrimethylammonium chloride homopolymer containing about 50%
by weight of the homopolymer in mineral oil or in a liquid ester can also be used. These
dispersions are sold under the names Salcare® SC 95 and Salcare® SC 96 by the company
Ciba.

(2) Cationic polysaccharides, especially cationic celluloses and galactomannan
gums. Among the cationic polysaccharides, mention may be made more particularly of
cellulose ether derivatives comprising quaternary ammonium groups, cationic cellulose
copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium
monomer and cationic galactomannan gums.
The cellulose ether derivatives comprising quaternary ammonium groups are
especially described in French patent 1 492 597, and mention may be made of the
polymers sold under the name Ucare Polymer "JR" (JR400 LT, JR 125 and JR 30M) or
"LR" (LR 400 or LR 30M) by the company Amerchol. These polymers are also defined in
the CTFA dictionary as quaternary ammoniums of hydroxyethylcellulose that have reacted
with an epoxide substituted with a trimethylammonium group.
Cationic cellulose copolymers or cellulose derivatives grafted with a water-
soluble quaternary ammonium monomer are described especially in US patent 4 131 576,
and mention may be made of hydroxyalkylcelluloses, for instance hydroxymethyl-,
hydroxyethyl- or hydroxypropylcelluloses grafted, in particular, with a
methacryloylethyltrimethylammoriium, methacrylamidopropyltrimethyl ammonium or
dimethyldiallylammonium salt. The commercial products corresponding to this definition
are more particularly the products sold under the names Celquat L 200 and Celquat H 100
by the company National Starch.
The cationic galactomannan gums are described more particularly in US
patents 3 589 578 and 4 031 307, and mention may be made of guar gums comprising
cationic trialkylammonium groups. Use is made, for example, of guar gums modified with
a 2,3-epoxyprbpyltrimethylammonium salt (for example, chloride). Such products are
especially sold under the names Jaguar C13 S, Jaguar C 15, Jaguar C 17 or Jaguar C162 by
the company Rhodia.
(3) Polymers formed from piperazinyl units and divalent alkylene or
hydroxyalkylene radicals containing straight or branched chains, optionally interrupted
with oxygen, sulfur or nitrogen atoms or with aromatic or heterocyclic rings, and also the
oxidation and/or quatemization products of these polymers.

(4) Water-soluble polyamino amides prepared in particular by
polycondensation of an acidic compound with a polyamine; these polyamino amides can
be crosslinked with an epihalohydrin, a diepoxide, a dianhydride, an unsaturated
dianhydride, a bis-unsaturated derivative, a bis-halohydrin, a bis-azetidinium, a bis-
haloacyldiamine, a bis-alkyl halide or alternatively with an oligomer resulting from the
reaction of a difunctional compound which is reactive with a bis-halohydrin, a bis-
azetidinium, a bis-haloacyldiamine, a bis-alkyl halide, an epihalohydrin, a diepoxide or a
bis-unsaturated derivative; the crosslinking agent being used in proportions ranging from
0.025 to 0.35 mol per amine group of the polyamino amide; these polyamino amides can
be alkylated or, if they comprise one or more tertiary amine functions, they can be
quatemized.
(5) Polyamino amide derivatives resulting from the condensation of
polyalkylene polyamines with polycarboxylic acids followed by alkylation with
bifunctional agents. Mention may be made, for example, of adipic
acid/dialkylaminohydroxyalkyldialkylenetriamine polymers in which the alkyl radical
comprises from 1 to 4 carbon atoms and preferably denotes methyl, ethyl or propyl.
Among these derivatives, mention may be made more particularly of the adipic
acid/dimethylaminohydroxypropyl/diethylenetriamine polymers sold under the name
Cartaretine F, F4 or F8 by the company Sandoz.
(6) Polymers obtained by reacting a polyalkylene polyamine comprising two
primary amine groups and at least one secondary amine group with a dicarboxylic acid
chosen from diglycolic acid and saturated aliphatic dicarboxylic acids containing from 3 to
8 carbon atoms; the mole ratio between the polyalkylene polyamine.and the dicarboxylic
acid preferably being between 0.8:1 and 1.4:1; the resulting polyamino amide being
reacted with epichlorohydrin in a mole ratio of epichlorohydrin relative to the secondary
amine group of the polyamino amide preferably of between 0.5:1 and 1.8:1. Polymers of
this type are sold in particular under the name Hercosett 57 by the company Hercules Inc.
or alternatively under the name PD 170 or Delsette 101 by the company Hercules in the
case of the adipic acid/epoxypropyl/diethylenetriamine copolymer.

(7) Cyclopolymers of alkyldiallylamine or of dialkyldiallylammonium, such as
the homopolymers or copolymers containing, as main constituent of the chain, units
corresponding to formula (I) or (II):

- k and t are equal to 0 or 1, the sum k +1 being equal to 1;
- R12 denotes a hydrogen atom or a methyl radical;
- R10 and R11, independently of each other, denote a C1-C6 alkyl group, a
hydroxyl(Cl-C5)alkyl group, a C1-C4 amidoalkyl group; or alternatively R10 and R11
may denote, together with the nitrogen atom to which they are attached, an heterocyclic
group such as piperidinyl or morpholinyl; R10 and Rll, independently of each other,
preferably denote a C1-C4 alkyl group;
- Y- is an anion such as bromide, chloride, acetate, borate, citrate, tartrate,
bisulfate, bisulfite, sulfate or phosphate.
Mention may be made more particularly of the dimethyldiallylammonium salt
(for example chloride) homopolymer sold for example under the name Merquat 100 by the
company Nalco, and the copolymers of diallyldimethylammonium salts (for example
chloride) and of acrylamide, sold especially under the name Merquat 550 or Merquat

(8) Quaternary diammonium polymers comprising repeating units of formula:

in which:
- R13, R14, R15 and R16, which may be identical or different, represent
aliphatic, alicyclic or arylaliphatic radicals comprising from 1 to 20 carbon atoms, or C1-
C12 hydroxyalkylaliphatic radicals,
or else R13, R14, R15 and R16, together or separately, constitute, with the
nitrogen atoms to which they are attached, heterocycles optionally comprising a second
non-nitrogen heteroatom,
or else R13, R14, R15 and R16 represent a linear or branched C1-C6 alkyl
radical substituted with a nitrile, ester, acyl, amide or -CO-O-R17-D or -CO-NH-R17-D
group in which R17 is an alkylene and D is a quaternary ammonium group;
- A1 and B1 represent divalent polymethylene groups comprising from 2 to 20
carbon atoms, linear or branched, saturated or unsaturated, and which may contain, linked
to or intercalated in the main chain, one or more aromatic rings or one or more oxygen or
sulfur atoms or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary
ammonium, ureido, amide or ester groups, and
- X- denotes an anion derived from a mineral or organic acid;
it being understood that Al, R13 and R15 can form, with the two nitrogen
atoms to which they are attached, a piperazine ring;
in addition, if Al denotes a linear or branched, saturated or unsaturated
alkylene or hydroxyalkylene radical, Bl may also denote a group (CH2)n-CO-D-OC-
(CH2)n- in which D denotes:
a) a glycol residue of formula -O-Z-O-, in which Z denotes a linear or
branched hydrocarbon-based radical, or a group corresponding to one of the following
formulae: -(CH2-CH2-O)x-CH2-CH2- and -[CH2-CH(CH3)-O]y-CH2-CH(CH3)-, where x
and y denote an integer from 1 to 4, representing a defined and unique degree of
polymerization or any number from 1 to 4 representing an average desree of

b) a bis-secondary diamine residue such as a piperazine derivative;
c) a bis-primary diamine residue of formula: -NH-Y-NH-, where Y denotes
a linear or branched hydrocarbon-based radical, or else the divalent radical
-CH2-CH2-S-S-CH2-CH2-;
d) a ureylene group of formula: -NH-CO-NH-;
Preferably, X- is an anion such as chloride or bromide. These polymers have a
number-average molar mass (Mn) generally of between 1000 and 100 000.
Mention may be made more particularly of polymers that are composed of
repeating units corresponding to the formula:

in which R1, R2, R3 and R4, which may be identical or different, denote an
alkyl or hydroxyalkyl radical containing from 1 to 4 carbon atoms, n and p are integers
ranging from 2 to 20, and X- is an anion derived from an organic or mineral acid.
A particularly preferred compound of formula (IV) is that for which R1, R2,
R3 and R4 represent a methyl radical and n = 3, p = 6 and X = C1, known as
Hexadimethrine chloride according to the INCI (CTFA) nomenclature.
(9) Polyquatemary ammonium polymers comprising units of formula (V):

in which:
- R18, R19, R20 and R21, which may be identical or different, represent a
hydrogen atom or a methyl, ethyl, propyl, β -hydroxyethyl, β-hydroxypropyl or

with the proviso that R18, R19, R20 and R21 do not simultaneously represent a hydrogen
atom,
- r and s, which may be identical or different, are integers between 1 and 6,
- q is equal to 0 or to an integer between 1 and 34,
- X- denotes an anion such as a halide,
- A denotes a dihalide radical or preferably represents -CH2-CH2-O-CH2-CH2-.
Examples that may be mentioned include the products Mirapol® A15,
Mirapol® AD1, Mirapol® AZ1 and Mirapol® 175 sold by the company Miranol.
(10) Quaternary polymers of vinylpyrrolidone and of vinylimidazole, for
instance the products sold under the names Luviquat® FC 905, FC 550 and FC 370 by the
company BASF.
(11) Polyamines such as Polyquart® H sold by Cognis, referred to under the
name Polyethylene glycol (15) tallow polyamine in the CTFA dictionary.
(12) Polymers comprising in their structure:
(a) one or more units corresponding to formula (A) below:

(b) optionally, one or more units corresponding to formula (B) below:

In other words, these polymers may be chosen especially from homopolymers
or copolymers comprising one or more units derived from vinylamine and optionally one
or more units derived from vinylformamide.
Preferably, these cationic polymers are chosen from polymers comprising, in

mol% of units corresponding to formula (A) and from 0 to 90 mol% of units corresponding
to formula (B).
These polymers may be obtained, for example, by partial hydrolysis of
polyvinylformamide. This hydrolysis may be performed in an acidic or basic medium.
The weight-average molecular mass of the said polymer, measured by light
scattering, may range from 1000 to 3 000 000 g/mol, preferably from 10 000 to
1 000 000 g/mol and more particularly from 100 000 to 500 000 g/mol.
The polymers comprising units of formula (A) and optionally units of formula
(B) are sold especially under the name Lupamin by the company BASF, for instance, and
in a non-limiting manner, the products sold under the names Lupamin 9095, Lupamin
5095, Lupamin 1095, Lupamin 9030 (or Luviquat 9030) and Lupamin 9010.
Other cationic polymers that may be used in the context of the invention are
cationic proteins or cationic protein hydrolysates, polyalkyleneimines, in particular
polyethyleneimines, polymers comprising vinylpyridine or vinylpyridinium units,
condensates of polyamines and of epichlorohydrin, quaternary polyureylenes and chitin
derivatives.
Preferably, the cationic polymers are chosen from the polymers of families (1),
(2), (7) and (10) mentioned above.
Among the cationic polymers mentioned above, the ones that may preferably
be used are cationic polysaccharides, especially cationic celluloses and galactomannan
gums, and in particular quaternary cellulose ether derivatives such as the products sold
under the name "JR 400" by the company Amerchol, cationic cyclopolymers, in particular
dimethyldiallylammohium salt (for example chloride) homopolymers or copolymers, sold
under the names Merquat 100, Merquat 550 and Merquat S by the company Nalco,
quaternary polymers of vinylpyrrolidone and of vinylimidazole, optionally crosslinked
homopolymers or copolymers of methacryloyloxy(C1-C4)alkyltri(Cl-C4)alkylammonium
salts, and mixtures thereof.
It is also possible to use amphoteric polymers, which may preferably be chosen

(i) one or more units derived from a monomer of (meth)acrylamide type,
(ii) one or more units derived from a monomer of
(meth)acrylamidoalkyltrialkylammonium type, and
(iii) one or more units derived from an acidic monomer of (meth)acrylic acid
type.
Preferably, the units derived from a monomer of (meth)acrylamide type (i) are
units of structure (la) below:

in which R1 denotes H or CH3 and R2 is chosen from an amino, dimethylamino,
tert-butylamino, dodecylamino or -NH-CH2OH radical.
Preferably, the said amphoteric polymer comprises a repetition of only one unit
of formula (Ia).
The unit derived from a monomer of (meth)acrylamide type of formula (Ia) in
which R1 denotes H and R2 is an amino radical (NH2) is particularly preferred. It
corresponds to the acrylamide monomer per se.
Preferably, the units derived from a monomer of
(meth)acrylamidoalkyltrialkylammonium type (ii) are units of structure (IIa) below:

in which:

- R4 denotes a group (CH2)k with k being an integer ranging from 1 to 6 and
preferably from 2 to 4;
- R5, R6 and R7, which may be identical or different, denote an alkyl group
containing from 1 to 4 carbon atoms;
- Y- is an anion such as bromide, chloride, acetate, borate, citrate, tartrate,
bisulfate, bisulfite, sulfate or phosphate.
Preferably, the said amphoteric polymer comprises a repetition of only one unit
of formula (Ha).
Among these units derived from a monomer of
(meth)acrylamidoalkyltrialkylammonium type of formula (Ha), the ones that are preferred
are those derived from the methacrylamidopropyltrimethylammonium chloride monomer,
for which R3 denotes a methyl radical, k is equal to 3, R5, R6 and R7 denote a methyl
radical, and Y" denotes a chloride anion.
Preferably, the units derived from a monomer of (meth)acrylic acid type (iii)
are units of formula (Ilia):

in which R8 denotes H or CH3 and R9 denotes a hydroxyl radical or a
-NH-C(CH3)2-CH2-SO3H radical.
The preferred units of formula (IIIa) correspond to the acrylic acid, methacrylic
acid and 2-acrylamino-2-methylpropanesulfonic acid monomers.
Preferably, the unit derived from a monomer of (meth)acrylic acid type of
formula (IIIa) is that derived from acrylic acid, for which R8 denotes a hydrogen atom and
R9 denotes a hydroxyl radical.
The acidic monomer(s) of (meth)acrylic acid type may be non-neutralized or
partially or totally neutralized with an organic or mineral base.
Preferably, the said amphoteric polymer comprises a repetition of only one unit

According to a preferred embodiment of the invention, the amphoteric
polymer(s) of this type comprise at least 30 mol% of units derived from a monomer of
(meth)acrylamide type (i). Preferably, they comprise from 30 mol% to 70 moI% and more
preferably from 40 mol% to 60 mol% of units derived from a monomer of
(meth)acrylamide type.
The content of units derived from a monomer of
(meth)acrylamidoalkyltrialkylammonium type (ii) may advantageously be from 10 mol%
to 60 mol% and preferentially from 20 mol% to 55 mol%.
The content of units derived from an acidic monomer of (meth)acrylic acid
type (iii) may advantageously be from 1 mol% to 20 mol% and preferentially from 5 mol%
to 15 mol%.
According to a particularly preferred embodiment of the invention, the
amphoteric polymer of this type comprises:
- from 30 mol% to 70 mol% and more preferably from 40 mol% to 60 mol% of
units derived from a monomer of (meth)acrylamide type (i),
- from 10 mol% to 60 mol% and preferentially from 20 mol% to 55 mol% of
units derived from a monomer of (meth)acrylamidoalkyltrialkylammonium type (ii), and
- from 1 mol% to 20 mol% and preferentially from 5 mol% to 15 mol% of
units derived from a monomer of (meth)acrylic acid type (iii).
Amphoteric polymers of this type may also comprise additional units, other
than the units derived from a monomer of (meth)acrylamide type, of
(meth)acrylamidoalkyltrialkylammonium type and of (meth)acrylic acid type as described
above.
However, according to a preferred embodiment of the invention, the said
amphoteric polymers consist solely of units derived from monomers (i) of
(meth)acrylamide type, (ii) of (meth)acrylamidoalkyltrialkylammonium type and (iii) of
(meth)acrylic acid type.
As examples of amphoteric polymers that are particularly preferred, mention
may be made of acrylamide/methacrylamidopropyltrimethylammonium chloride/acrylic
acid terpolymers. Such polymers are listed in the CTFA Dictionary (International Cosmetic

especially sold under the names Merquat 2003 and Merquat 2003 PR by the company
Nalco.
As another type of amphoteric polymer that may be used, mention may also be
made of copolymers based on (meth)acrylic acid and on a dialkyldiallylammonium salt,
such as copolymers of (meth)acrylic acid and of dimethyldiallylammonium chloride. An
example that may be mentioned is Merquat 280 sold by the company Nalco.
The composition according to the invention may comprise the cationic and/or
amphoteric polymers, preferably in an amount ranging from 0.01 to 0.5% by weight
relative to the total weight of the composition.
Polyols
For the purpose of the present invention, the term "polyol" should be
understood to mean any organic molecule comprising at least two free hydroxy groups.
The composition according to the invention may comprise one or more
polyols(s) in an amount ranging from 0.1 to 20% by weight, preferably from 1 to 15% by
weight, relative to the total weight of the composition.
A polyol suitable for the invention may be a compound such as a saturated or
unsaturated, linear, branched or cyclic alkyl bearing, on the alkyl chain, at least two -OH
functions, in particular at least three -OH functions, and more particularly at least four
-OH functions.
The polyols advantageously suitable for the formulation of the foaming
cleansing composition according to the present invention are those having, in particular,
from 2 to 16 carbon atoms, preferably 3 to 8 carbon atoms.
Among polyols, the following may be cited: glycerin, sorbitol, 1,3-propanediol,
isoprene glycol, pentylene glycol, hexylene glycol, glycerol, glycols such as ethylene
glycol, propylene glycol, butylenes glycol, pentylene glycol, diethylene glycol, decylene
glycol, caprylyl glycol, polyethylene glycol such as PEG-8, polyglycerols, such as glycerol
oligomers, for instance diglycerol, erythritol, arabitol, adonitol, sorbitol, dulcitol, glucose,
fructose, xylose, trehalose, sucrose, maltose, saccharose and lactose, and mixtures thereof.

According to a preferred embodiment the following polyols may be used:
glycerin, sorbitol, propylene glycol, decylene glycol, caprylyl glycol, butylene glycol,
pentylene glycol, polyethylene glycol and mixtures thereof.
According to a particular embodiment of the present invention, the polyol is
not a polymer with repeating units.
According to a more particularly preferred embodiment, the polyol comprises
at least sorbitol.
Throughout the description, including the claims, the expression "comprising
a" should be understood as being synonymous with "comprising at least one", unless
otherwise specified.
The expressions "between ... and ..." and "ranging from ... to ..." should be
understood as meaning limits included, unless otherwise specified.
The examples that follow illustrate the present invention without limiting the
scope thereof.
The cleansing compositions described in the following examples are prepared
using the following general process:
1. Soap is formed in situ in the main vessel at 75-80 °C and mixing is started at low
speed for solubilization in water.
2. Preservatives, chelating agent and polyols are added to main vessel.
3. Viscosity enhancing polymer is dispersed at high speed keeping temperature of the
main vessel greater than 80°C.
4. Surfactants are added at 45 - 65 °C.
5. In case of acrylates based polymers and GHTC, polymer is dispersed in water at
room temperature and neutralized at later stage.
Ingredient amounts are indicated in the following examples in active material
weight percentages "%wgt".
Example 1: Selection of viscosity enhancing polymers
Formulations were made with different polymers mentioned below. The molar

The following polymers are tried:
1. Methocel K15M sold by Dow Chemical: Hydroxypropyl methyl cellulose
2. Natrosol 250 HHR sold by Hashland: Hydroxyethyl cellulose
3. Carbopol ultrez 20 sold by Lubrizol: Acrylates/C 10-30 Alkyl acrylate crosspolymer
4. Carbopol ETD 2020 sold byLubrizol: Acrylates/C 10-30 Alkyl acrylate
crosspolymer
5. Keltrol CG-T sold by CP Kelco: Xanthan gum
6. Jaguar C13-S sold by Solvay: Guar hydroxypropyl trimonium chloride (GHTC)
7. Benecel K100M sold by Ashland.: Hydroxypropylmethylcellulose with Hydroxy
propyl content of 7-12% and methoxyl content ranging from 20-24% showing a
viscosity of 75,000 to 140,000 mPa.s (viscosity of 2% solution water as measured
by Brookfiled (rotational) viscometer)
"comp" in the following table means that the composition is outside the scope
of the present invention and "inv" means that the corresponding composition illustrates the
invention as claimed.



It comes out that composition "Exp 1" and "Exp 7" both comply with the
transparency requirement. As far as viscosity is concerned, it comes out that "Exp 7"
shows a greater viscosity value, therefore constituting a preferred embodiment of the
invention.



Example 3: various molar ratios between fatty acid and neutralizing agent
A combination of C12 and C14 fatty acid soap gives desired creamy foam with
adequate foam volume.
Formulations were made with different molar ratios of fatty acids and
triethanolamine as mentioned below.



In the present formula architecture, the molar ratio between fatty acids and
triethanolamine gives satisfactory results in terms of transparency when 1:1.8 or above.
Example 4: utilization of the composition according to the invention
Compositions according to example 2 are applied on wet skin of the face.
Then, it is foamed and rinsed with water.
After washing, the skin is clean and moisturized in all cases.

CLAIMS
1. A transparent cleansing liquid composition containing, in a physiologically
acceptable aqueous medium:
- at least a soap,
- at least one foaming surfactant,
- at least an organic neutralizing agent present in a molar ratio between soap
and said organic neutralizing agent of at least 1:1.75, preferably of at least
1:1.8, and
- at least a viscosity enhancing polymer comprising at least a
hydroxy(C1-C6)alkyl(C1-C6)alkyl cellulose,
wherein said composition has a pH ranging from 8 to 9, preferably from 8 to
8.5.
2. A composition according to claim 1, wherein said soap is present in the
composition in an amount ranging from 2 to 7% by weight relative to the total weight of
the composition, in particular from 3 to 6% by weight and most preferably from 4 to 5% by
weight.
3. A composition according to claim 1 or 2, wherein the soap is an organic
soap of fatty acid from 10 to 22 carbon atoms, more preferably from 12 to 18 carbon atoms
and most preferably from 12 to 14 carbon atoms.
4. A composition according to anyone of the preceding claims, wherein the
fatty acid is selected among the caproic acid, capric acid, caprylic acid, oleic acid, linoleic
acid, Iauric acid, the myristic acid, the stearic acid, the palmitic acid and mixtures thereof.
5. A composition according to anyone of the preceding claims, wherein the
molar ratio between fatty acid to neutralization agent ranges from 1:1.75 to 1:3, in
particular from 1:1.8 to 1:2.5.
6. A composition according to anyone of the preceding claims, wherein the
hydroxy(C1-C6)alkyl(C1-C6)alkylcellulose is hydroxy(C1-C4)alkyl(C1-C4)alkyl cellulose
and is more particularly selected from hydroxymethylbutylcellulose,
hydroxyethylmethylcellulose, hydroxyethylbutylcellulose and
hydroxypropylmethylcellulose and mixtures thereof.

7. A composition according to anyone of the preceding claims, wherein the
viscosity of the viscosity enhancing polymer, when present in an aqueous solution at a
weight concentration of 2%, varies between 75 000 and 140 000 Pa.s.
8. A composition according to anyone of the preceding claims, wherein the
cellulose ether is a hydroxypropylmethylcellulose, and in particular presents a
hydroxypropyl content ranging from 7 to 12% by weight with respect to the total weight of
hydroxypropylmethylcellulose, and presents a methoxy content ranging from 20 to 24% by
weight with respect to the total weight of hydroxypropylmethylcellulose.
9. A composition according to anyone of the preceding claims, wherein the
viscosity enhancing polymer is present in the composition in an amount ranging from 0.2
to 6% by weight, in particular from 0.5 to 5% by weight, and more particularly from 0.8 to
1.2% by weight, with respect to the total weight of the composition.
10. A composition according to anyone of the preceding claims, wherein the
composition comprises at least one foaming surfactant chosen from anionic, amphoteric (or
zwitterionic), nonionic and/or cationic foaming surfactants, and mixtures thereof, the said
anionic surfactant being in particular chosen from alkyi sulfates, alkyl ether sulfates,
alkylamido ether sulfates, alkylaryl polyether sulfates, monoglyceride sulfates, alkyl
sulfonates or alpha olefin sulfonates, alkyiamide sulfonates, alkylarylsulfonates, paraffin
sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylamide sulfosuccinates,
alkyl sulfoacetates, acylsarcosinates, acylglutamates, alkyl sulphosuccinamates,
acylisethionates and N-acyl taurates, salts of alkyl monoesters and
polyglycosidepolycarboxylic acids, acyl lactylates, N-acyl glycinates, salts of
D-galactoside-uronic acids, salts of alkyl ether carboxylic acids, alkyl aryl ether carboxylic
acid salts, salts of alkyl amidoether carboxylic acids, sulfoacetates, sulfolaurates, and the
corresponding non-salt forms all of these compounds, the said amphoteric or zwitterionic
surfactant being in particular chosen from (C8-C2o)alkylbetaines, sulfobetaines,
(C8-C20)alkylsulfobetaines, (C8-C20)alkylamido(C1-C6)alkylbetaines,
(C8-C20)alkylamido(C1-C6)alkylsulfobetaines, (C8-C20)alkylamphoacetates,
(C8-C20)alkylamphodiacetates and mixtures thereof, and the said nonionic surfactant being
in particular chosen from alkyl polyglucosides, and the said cationic surfactant being in
particular chosen from optionally polyoxyalkylenated primary, secondary or tertiary fattv

quaternary di- or triammonium salts, quaternary ammonium salts containing one or more
ester functions, and mixtures thereof.
11. A composition according to anyone of the preceding claims, wherein the
foaming surfactant at least contains an anionic surfactant(s), and is in particular chosen
from (C6-C24)alkyl sulfates, (C6-C24)alkyl ether sulfates such as sodium lauryl ether sulfate,
isethionates, amino acids, in particular glycinates, such as sodium N-cocoyl glycinate, their
alkali salts, and mixtures thereof.
12. A composition according to anyone of the preceding claims, wherein the
foaming surfactant is present in the composition in an amount ranging from 0.5 to 10% by
weight, in particular from 2 to 8% by weight, and more particularly from 3 to 6% by
weight, with respect to the total weight of the composition.
13. A composition according to anyone of the preceding claims, wherein the
organic neutralizing agent is selected from aminoalcohols such as ethanolamine, amino
sugars, amino acids and their alkali salts.
14. A composition according to anyone of the preceding claims, wherein it
further comprises a polyol such as glycerin, sorbitol, propylene glycol, decylene glycol,
caprylyl glycol, butylene glycol, pentylene glycol, polyethylene glycol and mixtures
thereof.
15. A composition according to anyone of the preceding claims, presenting a
viscosity ranging from 0.1 to 3 Pa.s, in particular from 0.2 to 2 Pa.s, and more particularly
from 0.3 to 1.3Pa.s.
16. Process for cleansing keratin materials, which consists in applying to the
said keratin materials a composition according to any one of the preceding claims,
eventually with water, followed by rinsing with water to eliminate foam and dirt.

Documents

Application Documents

# Name Date
1 1114-KOL-2014-(31-10-2014)-SPECIFICATION.pdf 2014-10-31
1 1114-KOL-2014-AbandonedLetter.pdf 2024-06-19
2 1114-KOL-2014-(31-10-2014)-GPA.pdf 2014-10-31
2 1114-KOL-2014-FORM 4(ii) [18-03-2020(online)].pdf 2020-03-18
3 1114-KOL-2014-FER.pdf 2019-09-19
3 1114-KOL-2014-(31-10-2014)-FORM-5.pdf 2014-10-31
4 1114-KOL-2014-FORM 18 [20-08-2018(online)].pdf 2018-08-20
4 1114-KOL-2014-(31-10-2014)-FORM-3.pdf 2014-10-31
5 1114-KOL-2014-(31-10-2014)-FORM-2.pdf 2014-10-31
5 1114-KOL-2014-(28-10-2015)-CORRESPONDENCE.pdf 2015-10-28
6 1114-KOL-2014-(31-10-2014)-FORM-1.pdf 2014-10-31
6 1114-KOL-2014-(21-04-2015)-ASSIGNMENT.pdf 2015-04-21
7 1114-KOL-2014-(31-10-2014)-DESCRIPTION (COMPLETE).pdf 2014-10-31
7 1114-KOL-2014-(21-04-2015)-CORRESPONDENCE.pdf 2015-04-21
8 1114-KOL-2014-(31-10-2014)-ABSTRACT.pdf 2014-10-31
8 1114-KOL-2014-(31-10-2014)-CORRESPONDENCE.pdf 2014-10-31
9 1114-KOL-2014-(31-10-2014)-CLAIMS.pdf 2014-10-31
10 1114-KOL-2014-(31-10-2014)-CORRESPONDENCE.pdf 2014-10-31
10 1114-KOL-2014-(31-10-2014)-ABSTRACT.pdf 2014-10-31
11 1114-KOL-2014-(31-10-2014)-DESCRIPTION (COMPLETE).pdf 2014-10-31
11 1114-KOL-2014-(21-04-2015)-CORRESPONDENCE.pdf 2015-04-21
12 1114-KOL-2014-(31-10-2014)-FORM-1.pdf 2014-10-31
12 1114-KOL-2014-(21-04-2015)-ASSIGNMENT.pdf 2015-04-21
13 1114-KOL-2014-(31-10-2014)-FORM-2.pdf 2014-10-31
13 1114-KOL-2014-(28-10-2015)-CORRESPONDENCE.pdf 2015-10-28
14 1114-KOL-2014-FORM 18 [20-08-2018(online)].pdf 2018-08-20
14 1114-KOL-2014-(31-10-2014)-FORM-3.pdf 2014-10-31
15 1114-KOL-2014-FER.pdf 2019-09-19
15 1114-KOL-2014-(31-10-2014)-FORM-5.pdf 2014-10-31
16 1114-KOL-2014-FORM 4(ii) [18-03-2020(online)].pdf 2020-03-18
16 1114-KOL-2014-(31-10-2014)-GPA.pdf 2014-10-31
17 1114-KOL-2014-AbandonedLetter.pdf 2024-06-19
17 1114-KOL-2014-(31-10-2014)-SPECIFICATION.pdf 2014-10-31

Search Strategy

1 sr1114_16-09-2019.pdf