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Ethane-1,2-diyl didecanoate, also known as di(decanoate) or bis(decanoate), is a chemical compound with the molecular formula C24H44O4. It is an ester derived from the reaction of ethane-1,2-diol (ethylene glycol) with two molecules of decanoic acid (capric acid). This organic compound is a colorless liquid with a density of approximately 0.92 g/cm3 and a melting point of -40°C. It is widely used in the production of various polymers, such as polyethylene terephthalate (PET), and as a plasticizer in the manufacturing of flexible materials. Additionally, it serves as a precursor in the synthesis of other chemicals and has applications in the pharmaceutical and cosmetic industries.

627-85-0

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627-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 627-85-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 627-85:
(5*6)+(4*2)+(3*7)+(2*8)+(1*5)=80
80 % 10 = 0
So 627-85-0 is a valid CAS Registry Number.

627-85-0SDS

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 2-decanoyloxyethyl decanoate

1.2 Other means of identification

Product number -
Other names Ethandioldidecanoat

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:627-85-0 SDS

627-85-0Downstream Products

627-85-0Relevant academic research and scientific papers

Structure and origin of artifacts in the analysis of plasmalogens

Dudda, Angela,Spiteller, Gerhard

, p. 303 - 308 (2007/10/03)

The determination of aldehydic compounds was achieved by gas chromatographic/mass spectrometric analysis of derived thioacetals. These were produced, together with artifacts, in a one-step reaction when plasmalogens were treated with ethane-1,2-dithiol and BF3. The artifacts Were recognized to be 2-alkylidene-1,3-dithiolanes derived from phospholipids. The latter were converted by BP, treatment into diacylglycerols, which were transformed in a complicated reaction into 2-alkyl-2-((2-mercaptoethyl)thiol-1,3-dithiolane. These compounds were decomposed thermally, e.g. in the injector of a gas chromatograph, in 2-alkylidene-1,3-dithiolanes, This reaction is not restricted to phospholipids but occurs with all monoacylated glycols.

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