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6975-33-3

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6975-33-3 Usage

Description

4-[(2-ethylhexyl)amino]-4-oxoisocrotonic acid is a chemical compound with the molecular formula C14H25NO3. It is known for its chelating and surfactant properties, making it a versatile substance in various industrial and research applications.

Uses

Used in Pharmaceuticals and Cosmetics:
4-[(2-ethylhexyl)amino]-4-oxoisocrotonic acid is used as a surfactant in pharmaceuticals and cosmetics for its ability to reduce surface tension and stabilize formulations.
Used in Metal Working Fluids and Drilling Fluids:
In the metalworking and drilling industries, 4-[(2-ethylhexyl)amino]-4-oxoisocrotonic acid is used as a corrosion inhibitor to protect metal surfaces from degradation and wear.
Used as a Chelating Agent:
4-[(2-ethylhexyl)amino]-4-oxoisocrotonic acid is used as a chelating agent in metal-ion complexation, which is important for various chemical processes and reactions.
Used in Chemical Synthesis:
4-[(2-ethylhexyl)amino]-4-oxoisocrotonic acid can also act as an intermediate to synthesize other organic compounds, contributing to the development of new chemical products.
Solubility:
4-[(2-ethylhexyl)amino]-4-oxoisocrotonic acid is soluble in organic solvents such as ethanol and acetone, and it is sparingly soluble in water, which further broadens its range of applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6975-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6975-33:
(6*6)+(5*9)+(4*7)+(3*5)+(2*3)+(1*3)=133
133 % 10 = 3
So 6975-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO3/c1-3-5-6-10(4-2)9-13-11(14)7-8-12(15)16/h7-8,10H,3-6,9H2,1-2H3,(H,13,14)(H,15,16)/b8-7-

6975-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-ethylhexylamino)-4-oxobut-2-enoic acid

1.2 Other means of identification

Product number -
Other names -

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:6975-33-3 SDS

6975-33-3Downstream Products

6975-33-3Relevant articles and documents

CLEAVABLE ADDITIVES FOR USE IN A METHOD OF MAKING A SEMICONDUCTOR SUBSTRATE

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Paragraph 0132, (2020/02/15)

The use of an organic compound as cleavable additive, preferably as cleavable surfactant, in the modification and/or treatment of at least one surface of a semiconductor substrate is described. Moreover, it is described a method of making a semiconductor substrate, comprising contacting at least one surface thereof with an organic compound, or with a composition comprising it, to treat or modify said surface, cleaving said organic compound into a set of fragments and removing said set of fragments from the contacted surface. More in particular, a method of cleaning or rinsing a semiconductor substrate or an intermediate semiconductor substrate is described. In addition, a compound is described which is suitable for the uses and methods pointed out above and which preferably is a cleavable surfactant.

Synthesis and physicochemical properties of strong electron acceptor 14,14,15,15-tetracyano-6,13-pentacenequinodimethane (TCPQ) diimide

Li, Jie,Xiong, Yu,Wu, Qinghe,Wang, Shitao,Gao, Xike,Li, Hongxiang

supporting information, p. 6136 - 6139,4 (2020/09/16)

14,14,15,15-Tetracyano-6,13-pentacenequinodimethane (TCPQ) diimide, a new tetracyanoquinodimethane analogue with extended conjugation and imide substituents, was synthesized by double Diels-Alder reactions and a Knoevenagel condensation reaction. Experimental results showed that TCPQ diimide has a low LUMO energy level (-4.03 eV) and good solubility in organic solvents.

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