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6829-42-1

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6829-42-1 Usage

General Description

DIETHYL-3-METHYLGLUTARATE is a chemical compound with the molecular formula C9H16O4. It is a diethyl ester derivative of 3-methylglutaric acid and is commonly used as a flavoring agent in the food and beverage industry. It is also used in the production of fragrances and as a solvent in various industrial applications. DIETHYL-3-METHYLGLUTARATE is known for its fruity and sweet odor, making it a popular ingredient in perfumes and cosmetic products. It is important to handle this chemical with care as it may cause irritation to the eyes, skin, and respiratory system if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 6829-42-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,2 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6829-42:
(6*6)+(5*8)+(4*2)+(3*9)+(2*4)+(1*2)=121
121 % 10 = 1
So 6829-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O4/c1-4-13-9(11)6-8(3)7-10(12)14-5-2/h8H,4-7H2,1-3H3

6829-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 3-methylpentanedioate

1.2 Other means of identification

Product number -
Other names 3-methyl-glutaric acid diethyl ester

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:6829-42-1 SDS

6829-42-1Relevant articles and documents

PROCESS FOR DOUBLE CARBONYLATION OF ALLYL ALCOHOLS TO CORRESPONDING DIESTERS

-

Paragraph 0055; 0060; 0061, (2017/07/14)

The invention relates to a process for doubly carbonylating allyl alcohols to the corresponding diesters, wherein a linear or branched allyl alcohol is reacted with a linear or branched alkanol (alcohol) with supply of CO and in the presence of a catalytic system composed of a palladium complex and at least one organic phosphorus ligand and in the presence of a hydrogen halide selected from HCl, HBr and HI.

Tobacco smoke chemistry. 1. A chemical and mass spectrometric study of tobacco smoke alkyl 2-hydroxy-2-cyclopentenones.

Arnarp,Enzell,Petersson,Pettersson

, p. 839 - 854 (2007/10/02)

A series of alkyl 2-hydroxy-2-cyclopentenones, which comprise biologically and organoleptically active compounds, have been synthesized and subjected to high resolution mass spectrometric studies to clarify structurally significant fragmentation pathways. On the basis of these results, 26 alkyl 2-hydroxy-2-cyclopentenones were identified in the weakly acidic fraction of smoke condensate from American blend type cigarettes, eighteen of which had not been detected in tobacco smoke previously. The utility for identification purposes of the corresponding quinoxaline derivatives, obtained through condensation with o-phenylenediamine, is discussed.

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