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6622-06-6

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6622-06-6 Usage

General Description

N-tert-butyl-succinamic acid, also known as N-TBSA, is a chemical compound with the molecular formula C10H19NO3. It is a white crystalline powder that is commonly used as a stabilizer in the synthesis of polymers and as an intermediate in the production of pharmaceuticals and agrochemicals. N-TBSA has been found to possess antioxidant and anti-inflammatory properties, and it is widely used in the food and beverage industry as a preservative to extend the shelf life of products. Additionally, it is used in personal care products and cosmetics as an emulsifier and stabilizer. Due to its versatility and beneficial properties, N-tert-butyl-succinamic acid is an important chemical in a variety of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6622-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6622-06:
(6*6)+(5*6)+(4*2)+(3*2)+(2*0)+(1*6)=86
86 % 10 = 6
So 6622-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO3/c1-8(2,3)9-6(10)4-5-7(11)12/h4-5H2,1-3H3,(H,9,10)(H,11,12)

6622-06-6SDS

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 4-(tert-butylamino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names N-tert-Butyl-succinamic acid

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:6622-06-6 SDS

6622-06-6Relevant articles and documents

Novel naphthalene-enoates: Design and anticancer activity through regulation cell autophagy

Di Yang, Meng,Shen, Xiao Bao,Hu, Yang Sheng,Chen, Yan Yan,Liu, Xin Hua

, (2019/03/09)

Eleven dihydroxy-2-(1-hydroxy-4-methylpent-3-enyl)naphthalene derivatives as anticancer agents through regulating cell autophagy were designed and synthesized. The anticancer activity results indicated that most compounds manifested obvious un-toxic effec

Facile syntheses and characterization of hyperbranched poly(ester-amide)s from commercially available aliphatic carboxylic anhydride and multihydroxyl primary amine

Li, Xiuru,Zhan, Jie,Li, Yuesheng

, p. 7584 - 7594 (2007/10/03)

A new method for synthesis of novel hyperbranched poly(ester-amide)s from commercially available AA′ and CBx type monomers has been developed on the basis of a series of model reactions. The hyperbranched poly(ester-amide)s with multihydroxyl end groups are prepared by thermal polycondensation of carboxyl anhydrides (AA′) and multihydroxyl primary amine (CBx) without any catalyst and solvent. The reaction mechanism in the initial stage of polymerization was investigated with in situ 1H NMR. In the initial stage of the reaction, primary amino groups of 2-amino-2-ethyl-1,3-propanediol (AEPO) or tris(hydroxymethyl)aminomethane (THAM) react rapidly with anhydride, forming an intermediate which can be considered as a new ABx type monomer. Further self-polycondensation reactions of the ABx molecules produce hyperbranched polymers. Analysis using 1H and 13C NMR spectroscopy revealed the degree of branching of the resulting polymers ranging from 0.36 to 0.55. These hyperbranched poly(ester-amide)s contain configurational isomers observed by 13C and DEPT 13C NMR spectroscopy, possess high molecular weights with broad distributions and display glass-transition temperatures (Tgs) between 7 and 96°C. The thermogravimetric analytic measurements revealed the decomposition temperature at 10% weight-loss temperatures (Td10%) ranging from 212 to 325°C. Among the hyperbranched poly(ester-amide)s obtained, the polymers with cyclohexyl molecular skeleton structure exhibit the lowest branching degree, the highest glass-transition temperatures, and the best thermal stability.

MEDICINAL COMPOSITIONS CONTAINING GABAPENTIN OR PREGABALIN AND N-TYPE CALCIUM CHANNEL ANTAGONIST

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Page/Page column 33, (2010/02/09)

The present invention relates to a pharmaceutical composition useful for preventing/treating pain, which comprises combination of gabapentin or pregabalin, or pharmaceutically acceptable salts thereof and N-type calcium channel antagonists or pharmaceutically acceptable salts thereof such as a compound having the following structure.

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