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Butanedioic acid, dodecyl-, dimethyl ester, also known as dimethyl azelate, is a chemical compound with the molecular formula C17H32O4. It is an ester derived from butanedioic acid (succinic acid) and dodecanol (1-dodecanol), where the hydroxyl group of the alcohol is replaced by a methyl group. This organic compound is a colorless liquid with a mild, pleasant odor and is commonly used as a solvent, plasticizer, and emollient in various industrial applications, including the production of cosmetics, personal care products, and pharmaceuticals. It is also employed as a fragrance ingredient and a component in the synthesis of other chemicals. Dimethyl azelate is known for its low toxicity and is generally considered safe for use in consumer products.

1472-86-2

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1472-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1472-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1472-86:
(6*1)+(5*4)+(4*7)+(3*2)+(2*8)+(1*6)=82
82 % 10 = 2
So 1472-86-2 is a valid CAS Registry Number.

1472-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-dodecylsuccinate

1.2 Other means of identification

Product number -
Other names Methyl-(n-dodecyl-succinat)

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:1472-86-2 SDS

1472-86-2Downstream Products

1472-86-2Relevant academic research and scientific papers

Selective Mono- and Bis(alkoxycarbonylation)s of Olefins Catalyzed by Palladium in the Presence of Cu(I) or Cu(II) Chloride under Remarkably Mild Conditions. Application to the Synthesis of γ-Butyrolactone Derivatives

Toda, Shiho,Miyamoto, Masanori,Kinoshita, Hideki,Inomata, Katsuhiko

, p. 3600 - 3606 (2007/10/02)

Palladium-catalyzed mono- and bis(alkoxycarbonylation)s of the olefins were controlled by the use of copper(II) and copper(I) chloride, respectively, in alcohol under normal pressure of carbon monoxide and oxygen at room temperature without any other additives. 3-Buten-1-ols gave the corresponding γ-butyrolactones and 2-oxotetrahydrofuran-3-acetic acid esters, respectively, in high yields.

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