The present disclosure relates to a process for preparing 3-methylbenzo-5,6-quinoline.
The process involves desulphonating 2-aminonaphthalene-1-sulphonic acid, followed by the addition of at least one aldehyde and at least one oxidizing agent to obtain 3-methylbenzo-5,6-quinoline. The process of the present disclo...
The present disclosure relates to a process for the preparation of 4-ethanesulfonyl-2-nitroaniline.
4-Ethanesulfonyl-2-nitroaniline is used as an intermediate for preparing dyes and pH indicators. It is also used in the manufacturing of UV stabilizers and optical brighteners. 4-Ethanesulfonyl-2-nitroaniline is rep...
The present disclosure relates to a process for the synthesis of benzothiazoles, with comparatively high yield and high purity. The process comprises chlorination of N-arylthiourea with a first chlorinating agent in the presence of a catalyst, followed by controlled chlorination with a second chlorinating agent and ...
The present disclosure relates to a process for the preparation of 1-methylhexyl(5-chloroquinolin-8-yloxy)acetate of Formula I:
1-Methylhexyl(5-chloroquinolin-8-yloxy)acetate is used as a safener with herbicides to protect crops from the incidental damage caused by herbicides. The process of the present disclosu...
The present disclosure relates to a process for the preparation of 2,6-dichloro-4-nitrophenol.
2,6-Dichloro-4-nitrophenol is an important intermediate in the agrochemical and the pharmaceutical industry. The present disclosure provides a simple, efficient, and eco-friendly process for the preparation of 2,6-dichlo...
The present disclosure relates to a process for the preparation of quinophthalone derivatives.
Quinophthalone derivatives are used as intermediates for many commercially important compounds such as pigments, dyes for synthetic fibers, plastic and ink-jet recording dyes. Some of the quinophthalone derivatives are a...
2-Nitro-4,5-dichloroacetanilide is an important intermediate in the dyestuff industry. In the present disclosure 2-nitro-4,5-dichloroacetanilide is prepared from 3,4-dichloroacetanilide using a nitrating agent in the presence of resultant sulfuric acid having strength of 104% w/w, in a simple, efficient and environm...
The present disclosure relates to azo dyes and a process for preparation thereof. The present disclosure provides azo dyes of formula I.
The azo dyes of the present disclosure being characterized by having ?max value in the range of 490 to 505 nm, thus resulting in vivid colors, especially reds, oranges, and ye...
In the present disclosure an azo disperse dye is prepared using an azo compound of formula (I) having ?max value of 495 nm.
The azo disperse dye is in the form of powder having average particle size in the range of 1 micron to 3 microns. The azo disperse dye is used to color the polyester fabrics in yellowish-r...
2-Nitro-45-dichloroacetanilide is an important intermediate in the dyestuff industry. In the present disclosure 2-nitro-45-dichloroacetanilide is prepared from 34-dichloroacetanilide using a nitrating agent in the presence of resultant sulfuric acid having strength of 104% w/w in a simple efficient and environmental...
[Class : 2] Dyes, Basic Dyes , Natural Dyes, Synthetic Dyes, Acid Dyes; Colorants And Pigments For Use In The Manufacture Of Pharmaceuticals; Pigments And Pigment Preparations; Dyes, Colorants, Pigments And Inks; Pigments For Use In The Manufacture Of Coloured Paper; Colorants For Use In The Manufacture Of Paper
[Class : 1] Chemical Intermediates For Use In Manufacture And Industry; Polymeric Intermediates, Chemicals For Use In Manufacturing Pharmaceuticals; Chemical Intermediates For Use In The Manufacture Of Agricultural Chemicals; Chemicals Used For The Formulation Of Hair Treatment Products; Reactive Liquid Polymer Compositions, Acids; Acetates; Chemicals For The Manufacture Of ...
[Class : 2] Dyes, Basic Dyes , Natural Dyes, Synthetic Dyes, Acid Dyes; Colorants And Pigments For Use In The Manufacture Of Pharmaceuticals; Pigments And Pigment Preparations; Dyes, Colorants, Pigments And Inks; Pigments For Use In The Manufacture Of Coloured Paper; Colorants For Use In The Manufacture Of Paper
View +1 more Brands for Amogh Chemicals Private Limited.
Charges
4 Crore
15 March 2019
Hdfc Bank Limited
4 Crore
23 January 2012
Citibank N.a
4 Crore
31 January 2012
Citi Bank N.a.
3 Crore
31 January 2012
Citibank N. A.
1 Crore
23 October 2008
Idbi Bank Limited
4 Crore
30 August 2008
Idbi Bank Limited
4 Crore
26 December 2006
Ruppe Co-operative Bank Ltd.
2 Crore
18 December 2002
Rupee Co-op Bank Ltd
25 Lak
10 January 2007
Rupee Co-operative Bank Ltd.
1 Crore
15 April 2004
Rupe Co-op Bank Ltd
20 Lak
10 January 2008
Rupee Co-operative Bank Ltd
15 Lak
15 October 2007
Rupee Co-operative Bank Ltd
1 Crore
31 March 2005
Rupe Co-op Bank Ltd
25 Lak
15 March 2019
Hdfc Bank Limited
0
31 March 2005
Rupe Co-op Bank Ltd
0
30 August 2008
Idbi Bank Limited
0
15 October 2007
Rupee Co-operative Bank Ltd
0
23 October 2008
Idbi Bank Limited
0
31 January 2012
Citibank N. A.
0
31 January 2012
Citi Bank N.a.
0
18 December 2002
Rupee Co-op Bank Ltd
0
15 April 2004
Rupe Co-op Bank Ltd
0
23 January 2012
Citibank N.a
0
26 December 2006
Ruppe Co-operative Bank Ltd.
0
10 January 2007
Rupee Co-operative Bank Ltd.
0
10 January 2008
Rupee Co-operative Bank Ltd
0
15 March 2019
Hdfc Bank Limited
0
31 March 2005
Rupe Co-op Bank Ltd
0
30 August 2008
Idbi Bank Limited
0
15 October 2007
Rupee Co-operative Bank Ltd
0
23 October 2008
Idbi Bank Limited
0
31 January 2012
Citibank N. A.
0
31 January 2012
Citi Bank N.a.
0
18 December 2002
Rupee Co-op Bank Ltd
0
15 April 2004
Rupe Co-op Bank Ltd
0
23 January 2012
Citibank N.a
0
26 December 2006
Ruppe Co-operative Bank Ltd.
0
10 January 2007
Rupee Co-operative Bank Ltd.
0
10 January 2008
Rupee Co-operative Bank Ltd
0
15 March 2019
Hdfc Bank Limited
0
31 March 2005
Rupe Co-op Bank Ltd
0
30 August 2008
Idbi Bank Limited
0
15 October 2007
Rupee Co-operative Bank Ltd
0
23 October 2008
Idbi Bank Limited
0
31 January 2012
Citibank N. A.
0
31 January 2012
Citi Bank N.a.
0
18 December 2002
Rupee Co-op Bank Ltd
0
15 April 2004
Rupe Co-op Bank Ltd
0
23 January 2012
Citibank N.a
0
26 December 2006
Ruppe Co-operative Bank Ltd.
0
10 January 2007
Rupee Co-operative Bank Ltd.
0
10 January 2008
Rupee Co-operative Bank Ltd
0
Documents
Form MSME FORM I-03122020_signed
Form MSME FORM I-17062020_signed
Instrument(s) of creation or modification of charge;-05022020
Form CHG-1-05022020_signed
CERTIFICATE OF REGISTRATION FOR MODIFICATION OF CHARGE-20200205
List of share holders, debenture holders;-25122019
Copy of MGT-8-25122019
Form MGT-7-25122019_signed
Directors report as per section 134(3)-11112019
Copy of Financial Staements duly authenticated as per section 134 (Including Boards report, auditors report and other documents)-11112019
Form AOC-4-11112019_signed
Form DPT-3-08112019-signed
Form MSME FORM I-26102019_signed
Form ADT-1-12102019_signed
Copy of resolution passed by the company-12102019
Copy of the intimation sent by company-12102019
Copy of written consent given by auditor-12102019
Form CHG-4-08072019_signed
Letter of the charge holder stating that the amount has been satisfied-08072019
CERTIFICATE OF SATISFACTION OF CHARGE-20190708
Optional Attachment-(1)-15062019
Form ADT-1-20042019_signed
Copy of resolution passed by the company-19042019
Copy of written consent given by auditor-19042019
Copy of the intimation sent by company-19042019
Form CHG-1-03042019_signed
Instrument(s) of creation or modification of charge;-03042019