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16369-12-3

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16369-12-3 Usage

Class

Alkenes

Properties

Long-chain unsaturated hydrocarbon compound
Colorless
Odorless
Insoluble in water
Soluble in organic solvents

Uses

Starting material in the synthesis of various organic compounds
Used in the production of surfactants, lubricants, and polymers
Chemical intermediate in the production of fragrances, flavors, and pharmaceuticals
Potential application as a renewable biofuel for its high energy density and low toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 16369-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16369-12:
(7*1)+(6*6)+(5*3)+(4*6)+(3*9)+(2*1)+(1*2)=113
113 % 10 = 3
So 16369-12-3 is a valid CAS Registry Number.

16369-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-HEPTADECENE

1.2 Other means of identification

Product number -
Other names heptadec-8c-ene

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:16369-12-3 SDS

16369-12-3Relevant articles and documents

Electrochemistry for biofuel generation: Transformation of fatty acids and triglycerides to diesel-like olefin/ether mixtures and olefins

Dos Santos, Tatiane R.,Harnisch, Falk,Nilges, Peter,Schr?der, Uwe

, p. 886 - 893 (2015/06/02)

Abstract Electroorganic synthesis can be exploited for the production of biofuels from fatty acids and triglycerides. With Coulomb efficiencies (CE) of up to 50%, the electrochemical decarboxylation of fatty acids in methanolic and ethanolic solutions leads to the formation of diesel-like olefin/ether mixtures. Triglycerides can be directly converted in aqueous solutions by using sonoelectrochemistry, with olefins as the main products (with a CE of more than 20%). The latter reaction, however, is terminated at around 50% substrate conversion by the produced side-product glycerol. An energy analysis shows that the electrochemical olefin synthesis can be an energetically competitive, sustainable, and - in comparison with established processes - economically feasible alternative for the exploitation of fats and oils for biofuel production. From fat to fuel: Electrochemical decarboxylation of fatty acids and triglycerides leads to the formation of olefins and ethers (see scheme). This electroorganic synthesis is an energetically competitive, sustainable, and economically feasible alternative for the exploitation of fats and oils for biofuel production.

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