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3,3-Diethylpentanedioic acid, also known as 3,3-diethylglutaric acid, is an organic compound with the chemical formula C9H16O4. It is a white crystalline solid that is soluble in water and has a molecular weight of 192.22 g/mol. This dicarboxylic acid is characterized by a pentane backbone with two carboxyl groups (-COOH) at the terminal ends and two ethyl groups (-CH2CH3) attached to the third carbon atom. 3,3-Diethylpentanedioic acid is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the production of polymers and as a chelating agent in various industrial processes.

4160-95-6

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4160-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4160-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4160-95:
(6*4)+(5*1)+(4*6)+(3*0)+(2*9)+(1*5)=76
76 % 10 = 6
So 4160-95-6 is a valid CAS Registry Number.

4160-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-diethylpentanedioic acid

1.2 Other means of identification

Product number -
Other names 3,3-Diethylglutaric 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:4160-95-6 SDS

4160-95-6Relevant academic research and scientific papers

Geminate-Substituted Cyclopentadienes. 1. Synthesis of 5,5-Dialkylcyclopentadienes via 4,4-Dialkylcyclopent-2-en-1-ones.

Holder, Richard W.,Daub, John P.,Baker, Wesley E.,Gilbert, Raymond H,Graf, Norman A.

, p. 1445 - 1451 (2007/10/02)

A synthetic route for the preparation of 5,5,-dialkylcyclopentadienes (1) via 4,4-dialkylcyclopent-2-en-1-ones (3) is described.Beginnig with ketones (in which the two carbonyl substituents will become the two alkyl groups in the title compounds), the route traverses the Guareschi imides 5, 3,3-dialkylglutaric acids 4 and their ethyl esters 7, masked acyloins 8, cyclopentenones 3, alkohols 9, and bromides 10 to reach the dienes 1.Physical properties of five such derivates 1 and 3 (dimethyl, methylethyl,diethyl, methyl-n-propyl, and methylisopropyl) are presented.

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