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6183-35-3

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6183-35-3 Usage

General Description

1,2,4,5-Benzenetetracarboxamide, also known as BTCA, is a chemical compound made up of a benzene ring with four carboxamide groups attached to it. It is commonly used as a cross-linking agent in the production of synthetic fibers, particularly in the manufacturing of nylon. BTCA is also utilized as a flame retardant in textiles and plastics, as well as a coating and adhesive in various industrial applications. Additionally, it is employed as a corrosion inhibitor in metalworking fluids. BTCA is known for its high thermal stability and resistance to chemicals, making it an effective and versatile additive in a wide range of industrial processes. However, there are concerns about its potential environmental and human health impacts, particularly due to its persistence and potential for bioaccumulation.

Check Digit Verification of cas no

The CAS Registry Mumber 6183-35-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6183-35:
(6*6)+(5*1)+(4*8)+(3*3)+(2*3)+(1*5)=93
93 % 10 = 3
So 6183-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N4O4/c11-7(15)3-1-4(8(12)16)6(10(14)18)2-5(3)9(13)17/h1-2H,(H2,11,15)(H2,12,16)(H2,13,17)(H2,14,18)

6183-35-3 Well-known Company Product Price

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  • Aldrich

  • (472115)  1,2,4,5-Benzenetetracarboxamide  97%

  • 6183-35-3

  • 472115-5G

  • 919.62CNY

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6183-35-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,2,4,5-tetracarboxamide

1.2 Other means of identification

Product number -
Other names Pyromellitamid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6183-35-3 SDS

6183-35-3Relevant articles and documents

Corresponding amine nitrile and method of manufacturing thereof

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Paragraph 0122; 0123; 0127; 0129, (2018/05/24)

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Corresponding amine nitrile and method of manufacturing thereof (by machine translation)

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Paragraph 0123-0124; 0129-0130, (2017/10/22)

The invention relates to a method of manufacturing one kind of nitrile, compared with the prior art, has significantly reduced the amount of ammonia, the environmental pressure of the small, low energy consumption, low production cost, nitrile product purity and yield and the like, and can obtain more complex structure of the nitriles. The invention also relates to the corresponding amine by the nitrile manufacture method. (by machine translation)

Octaalkyl Esters of 2,3,9,10,16,17,23,24-(29H,31H)-Phthalocyanineoctacarboxylic Acid: A New Homologous Series of Discotis Liquid Crystals

Dulog, Lothar,Gittinger, Andreas

, p. 31 - 42 (2007/10/02)

The synthesis of a homologous series of octaalkoxycarbonyl-substitued metal-free phthalocyanines (Pc) is described.The mesomorphic properties of these new materials were studied by differential scanning calorimetry (DSC), optical microscopy and X-ray investigations.All compounds show a discotic mesophase in an extremely large temperature interval including room temperature.X-ray diffraction patterns of the mesophases confirm that all compounds form a hexagonal columnar mesophase of the type Dho.

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