Company Information
CIN
Status
Date of Incorporation
23 August 1948
State / ROC
Mumbai / ROC Mumbai
Last Balance Sheet
31 March 2023
Last Annual Meeting
15 June 2023
Paid Up Capital
194,468,890
Authorised Capital
2,288,878,000
Directors
Ramakrishnan Mukundan
Director/Designated Partner
over 2 years ago
over 2 years ago
Rakesh Radheyshyam Jhunjhunwala
Beneficial Owner
almost 6 years ago
almost 6 years ago
Punita Kumar Sinha
Director/Designated Partner
over 6 years ago
over 6 years ago
Sanjiv Lal
Director/Designated Partner
over 6 years ago
over 6 years ago
Yashaswin Narendra Sheth
Manager/Secretary
almost 7 years ago
almost 7 years ago
Bhaskar Bhat .
Director/Designated Partner
over 9 years ago
over 9 years ago
Prasad Raghava Menon
Director
over 22 years ago
over 22 years ago
Past Directors
Padmini Bhalchandra Khare
Director
over 8 years ago
over 8 years ago
Collur Visweswaria Natraj
Additional Director
over 9 years ago
over 9 years ago
Ashish Priyakant Mehta
Cfo(kmp)
over 11 years ago
over 11 years ago
Veeramani Shankar
Ceo(kmp)
over 11 years ago
over 11 years ago
Yashwant Shankarrao Patil Thorat
Director
over 13 years ago
over 13 years ago
Yoginder Kumar Alagh
Additional Director
over 15 years ago
over 15 years ago
Prabhakaran Nair
Director
over 16 years ago
over 16 years ago
Venkatrao Shridhar Sohoni
Director
over 17 years ago
over 17 years ago
Prakash Ranjan Rastogi
Director
over 18 years ago
over 18 years ago
Bharat Damodar Vasani
Director
over 18 years ago
over 18 years ago
Eknath Atmaram Kshirsagar
Director
almost 20 years ago
almost 20 years ago
Brajadas Banerjee
Director
over 21 years ago
over 21 years ago
Pouruchisti Shahrukh Meherhomji
Company Secretary
about 22 years ago
about 22 years ago
Homi Rustam Khusrokhan
Director
over 22 years ago
over 22 years ago
Ramabadran Gopalakrishnan
Director
over 26 years ago
over 26 years ago
Russi Jal Taraporevala
Director
about 37 years ago
about 37 years ago
Ram Sukhraj Tarneja
Director
over 40 years ago
over 40 years ago
Patents
The present disclosure provides a process for preparation of a compound of formula 1, or isomers or its derivatives thereof, which show a high herbicidal activity against wide variety of weeds.
wherein R1 is a C3-C4 alkynyl group, a C1-C5 alkyl group, or a C3-C4 alkenyl group, and X is selected from the group consi...
The present disclosure provides a compound of formula I, its derivatives, salts, stereoisomers, or regio-isomers thereof, useful as intermediates in preparation of sulfonamide or sulfonyl urea growth regulators or herbicides.
The present disclosure further provides process for preparing compound of formula I, its d...
The present invention relates to an improved process for the preparation of substantially pure crystalline pendimethalin. More particularly the present invention relates to the conversion of crude pendimethalin to substantially pure crystals of pendimethalin at safe operating temperature below 90°C employing the met...
A process for preparation of Lambda cyhalothrin of formula I which is useful as an insecticide with contact and stomach action and repellant properties and is used to control a wide variety of insect pests like aphids, thrips, Lepidoptera larvae, Coleoptera larvae and adults, comprises the epimerization of cis- cyha...
The invetion disclosed in this application relates to novel 2-chloro-5-pyridymethyl and its derivaties having the general formula I
Where : X = Halogtens and R= Chloro Thiazole Group and its derivatives useful as broad spectrum insecticide. Particularly the invention relates to novel N-(2-Chloro-5-pyridylmethyl)-...
We Claim:
1. A process for the preparation of Pendimethalln (I) as shown in the accompanying drawing sheets in which 3,4-xylidine is condensed with Diethylketone in presence of a solvent, catalyst, under a temperature range of 50-110°C, which would enable the azeotropic distillation of
The present invention relates to cloning and characterization of Coat Protein (CP) gene of Chilli Leaf Curl Virus (ChCV) and the recombinant DNA molecules derived comprising one or more DNA sequences showing at least 80% homology to the ChLCV coat protein gene sequence. Further to the plants transformed therewith th...
The present invention relates to an improved process for the synthesis of E-isomer of compound of formula (5). It further relates to the conversion of formula (5), wherein R is H, to Intermediate (I) and subsequently to substantially pure Trifloxystrobin, compound of formula (I) in good yield.
The present invention relates to an improved process for the synthesis of strobilurin fungicides viz Kresoxim-methyl, Dimoxystrobin and Orysastrobin in good yield and high purity.
The present disclosure relates to technical field of agricultural insecticide. In particular, the present disclosure relates to a new and improved formulation comprising a combination of Lambda-cyhalothrin and Fipronil as active ingredients, along with one or more agrochemical excipients, for protecting agricultural...
The present disclosure provides a compound of formula I, its derivatives, salts, stereo-isomers, or regio-isomers thereof, useful as intermediates in preparation of sulfonamide or sulfonyl urea growth regulators or herbicides.
The present disclosure further provides process for preparing compound of formula I, its ...
The present disclosure provides a new and improved process for preparation of intermediate compounds and synthesis of mesotrione therefrom. The present disclosure provides an economical, efficient and eco-friendly process for preparation of mesotrione.
The present disclosure provides a synergistic herbicide composition comprising combination of bispyribac-sodium, metsulfuron-methyl and pyrazosulfuron-ethyl. The ternary herbicide composition is suitable for selectively controlling undesirable vegetation in crops of agriculturally useful plants and exhibits a synerg...
The current invention relates to methods and compositions to select herbicide- resistant maize plants, by using molecular markers. It more specifically relates to novel single nucleotide polymorphism markers linked with 4-hydroxyphenylpyruvate dioxygenase inhibitor resistance in maize plants, and methods for identif...
The present disclosure provides a herbicidal synergistic composition and formulations comprising combination of pretilachlor, pyrazosulfuron-ethyl and chlorimuron. The ternary herbicide composition is suitable for selectively controlling undesirable vegetation in crops of agriculturally useful plants and exhibits a ...
The present disclosure relates to a composition comprising active ingredients chlorantraniliprole, acetamiprid and lambda-cyhalothrin. Particularly, the present disclosure provides an insecticide composition comprising three active ingredients chlorantraniliprole, acetamiprid and lambda-cyhalothrin in combination wi...
The present disclosure provides a herbicide composition comprising combination of metsulfuron-methyl, clodinafop-propargyl and metribuzin. The present invention also provides a process for preparing the herbicide composition. The herbicide composition is stable and exhibits a synergistic herbicidal activity in contr...
The present disclosure relates to a composition comprising three active ingredients emamectin benzoate, fipronil, lambda-cyhalothrin and one or more inactive excipient(s) selected from the group comprising of a pH stabilizer, an emulsifier, a dispersing agent, stabilizing agent, wetting agent, spreading agent, anti-...
The present invention relates to an insecticide composition comprising emamectin benzoate, acetamiprid, lambda-cyhalothrin and inactive excipients and its process for preparation thereof.
The present invention relates to a binary herbicidal composition comprising 4-amino-6-tert-butyl-3-(methylthio)-1,2,4-triazin-5(4H)-one (metribuzin) and ethyl 5-{[(4,6-dimethoxypyrimidin-2-yl)carbamoyl]sulfamoyl}-1-methyl-1H-pyrazole-4-carboxylate (pyrazosulfuron-ethyl) and a stabilizing agent for control of weeds, ...
The present disclosure relates to a composition and a formulation comprising active ingredients trifloxystrobin, difenoconazole and polymeric surfactant. Particularly, the present disclosure provides a suspension concentrate (SC) formulation comprising the active ingredients trifloxystrobin, difenoconazole and polym...
ABSTRACT
MOLECULAR MARKERS ASSOCIATED WITH NORTHERN CORN LEAF BLIGHT RESISTANCE IN MAIZE
The current invention relates to methods and compositions to select northern corn blight-or Exserohilum resistant maize plants, by using molecular markers. It more specifically relates to novel single nucleotide polymorphism m...
“METHODS FOR DETECTING SINGLE NUCLEOTIDE POLYMORPHISM (SNP) AS MARKER FOR GENETIC MALE STERILITY (GMS) IN CAPSICUM ANNUUM”
ABSTRACT
The present disclosure provides methods for identifying presence or absence of a gene associated with genetic male sterility (GMS) in a Capsicum annuum plant. This is done by anal...
The present disclosure relates to a composition comprising active ingredients mesotrione, tembotrione and one or more agriculturally acceptable excipients selected from the group comprising of dispersing agent, wetting agent, anti-freezing agent, anti-foaming agent, biocide, rheology modifier and solvent and formula...
The present disclosure provides a new process for the preparation of bifenthrin and its intermediates. The present disclosure provides an easy, economical, eco-friendly, and efficient process for preparation of bifenthrin.
The present disclosure provides an improved process for the preparation of pure clomazone and an improved process for purification of crude clomazone. The present disclosure provides an easy, economical, efficient and eco-friendly process for preparation of clomazone.
The current invention relates to methods and compositions to identify and select genetically male sterile cotton plants, by using molecular markers. It more specifically relates to novel simple sequence repeat markers and primers for amplifying and identifying these markers in cotton plants, with the ms5ms6 double r...
The current invention relates to methods and compositions to identify and select male sterile cotton plants displaying genetic male sterility. The invention discloses novel single nucleotide polymorphic markers that are associated closely with ms5ms6 double recessive genotype in cotton plants. These molecular marker...
The present disclosure relates to a fungicide formulation comprising Metalaxyl-M and Kresoxim-methyl. The composition is formulated as a suspo-emulsion formulation (SE), a ZC formulation (ZC), or a micro-emulsion (ME) formulation. The composition achieves one or more advantages including ability to formulate desired...
The invention relates to an agrochemical formulation comprising prothioconazole and trifloxystrobin active ingredients, wherein the formulation is a water dispersible granule (WG) formulation or a wettable powder (WP) formulation and a process for preparing the formulations thereof. The invention particularly relate...
The invention relates to an agrochemical composition comprising metalaxyl-m, propineb and a film forming agent and formulations thereof, particularly wettable powder (WP) and water dispersible granule (WDG) formulations. The agrochemical formulation increases the rainfastness and has improved bio-efficacy thereby pr...
Registered Trademarks
[Class : 5] Pesticides, Insecticides, Fungicides, Herbicides, Weedicides, Disinfectants, Preparations For Destroying Vermin.
[Class : 31] Plant Seeds, Hybrid Seeds, Maize Seeds, Genetically Modified Seeds, All Kinds Of Agricultural Seeds Included In Class 31
[Class : 31] Plant Seeds, Hybrid Seeds, Cotton Seeds, Genetically Modified Seeds, All Kinds Of Agricultural Seeds Included In Class 31
View +662 more Brands for Rallis India Limited.
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Others
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Axis Bank Limited
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23 February 2012
Hdfc Bank Limited
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23 December 2002
Uco Bank
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24 January 2014
Icici Bank Limited
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22 May 2010
Biotechnology Industry Research Assistance Council
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01 August 1986
State Bank Of India
0
03 November 2014
Kotak Mahindra Bank Limited
0
28 March 2003
Indusind Bank Ltd
0
21 July 2015
Citi Bank N.a.
0
27 March 2015
Kotak Mahindra Bank Limited
0
17 January 2014
Kotak Mahindra Bank Limited
0
15 May 2012
Hdfc Bank Limited
0
27 January 2011
Axis Trustee Services Limited
0
25 March 2009
Axis Bank Limited
0
01 February 2011
Others
0
30 October 2006
State Bank Of India
0
29 March 2011
Others
0
17 July 2009
Axis Bank Limited
0
23 February 2012
Hdfc Bank Limited
0
23 December 2002
Uco Bank
0
24 January 2014
Icici Bank Limited
0
22 May 2010
Biotechnology Industry Research Assistance Council
0
01 August 1986
State Bank Of India
0
03 November 2014
Kotak Mahindra Bank Limited
0
28 March 2003
Indusind Bank Ltd
0
21 July 2015
Citi Bank N.a.
0
27 March 2015
Kotak Mahindra Bank Limited
0
17 January 2014
Kotak Mahindra Bank Limited
0
15 May 2012
Hdfc Bank Limited
0
27 January 2011
Axis Trustee Services Limited
0
25 March 2009
Axis Bank Limited
0
01 February 2011
Others
0
30 October 2006
State Bank Of India
0
29 March 2011
Others
0
17 July 2009
Axis Bank Limited
0
23 February 2012
Hdfc Bank Limited
0
23 December 2002
Uco Bank
0
24 January 2014
Icici Bank Limited
0
22 May 2010
Biotechnology Industry Research Assistance Council
0
01 August 1986
State Bank Of India
0
03 November 2014
Kotak Mahindra Bank Limited
0
28 March 2003
Indusind Bank Ltd
0
21 July 2015
Citi Bank N.a.
0
27 March 2015
Kotak Mahindra Bank Limited
0
17 January 2014
Kotak Mahindra Bank Limited
0
15 May 2012
Hdfc Bank Limited
0
27 January 2011
Axis Trustee Services Limited
0
25 March 2009
Axis Bank Limited
0
Documents
Form AOC-4(XBRL)-20072024_signed
Optional Attachment-(2)-19072024
Optional Attachment-(4)-19072024
Optional Attachment-(3)-19072024
Optional Attachment-(1)-19072024
Form MGT-15-09072024_signed
Form MSME FORM I-30042024_signed
Form MGT-6-17042024_signed
-17042024
Optional Attachment-(1)-17042024
Form Addendum to AOC-4 CSR-27032024_signed
Form MGT-6-28022024_signed
-28022024
Optional Attachment-(1)-28022024
Form MSME FORM I-05112023_signed
Form MGT-6-04092023_signed
Form MGT-7-03092023_signed
Form Addendum to AOC-4 CSR-01092023_signed
Form MSME FORM I-29082023_signed
Form MGT-15-24082023_signed
Form AOC-4(XBRL)-24082023_signed
R1ShareholdersMGT7mcaupload_F62828587_RALLIS123_20230804110922.xlsm
Form MGT-6-03082023_signed
-03082023
Form MGT-7-03082023_signed
Copy of MGT-8-02082023
Optional Attachment-(3)-02082023
Optional Attachment-(4)-02082023
Optional Attachment-(2)-02082023
Optional Attachment-(1)-02082023
