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(1-14C)heptadecanoic acid is a radiolabeled fatty acid with the chemical formula C16H32O2 and a molecular weight of 256.43 g/mol. It is a straight-chain, saturated fatty acid consisting of 17 carbon atoms, with the first carbon atom (ω-1 position) labeled with the radioactive isotope carbon-14 (14C). (1-~14~C)heptadecanoic acid is commonly used in biochemical research to study lipid metabolism, fatty acid oxidation, and the synthesis of complex lipids. The radiolabel allows for the tracking and quantification of heptadecanoic acid and its metabolic products in various biological systems, providing valuable insights into cellular processes and potential therapeutic targets for metabolic disorders.

98365-91-4

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98365-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98365-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,6 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98365-91:
(7*9)+(6*8)+(5*3)+(4*6)+(3*5)+(2*9)+(1*1)=184
184 % 10 = 4
So 98365-91-4 is a valid CAS Registry Number.

98365-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name heptadecanoic acid

1.2 Other means of identification

Product number -
Other names Heptadecanoic acid-1-14C 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:98365-91-4 SDS

98365-91-4Downstream Products

98365-91-4Relevant academic research and scientific papers

Pyrolysis of Alkyl Acetates. A Radical Pathway for the Formation of Minor Products

Shi, Buchang,Ji, Ying,Dabbagh, Hossein A.,Davis, Burtron H.

, p. 845 - 849 (2007/10/02)

Decyl acetate and decene pyrolysis under the same reaction conditions show that the formation of the minor products during the pyrolysis of esters occurs by a parallel, and not a secondary, reaction.The radioactivity observed in the CO2 and CO produced during the pyrolysis of 1-hexyl acetate-1-14C and the radioactivity in the methane from the pyrolysis of 1-hexyl acetate-2-14C strongly suggested a radical reaction pathway for the formation of the minor products.Considering the above results together with the radioactivity data of gas samples from the pyrolysis of 1-decyl-1-14C acetate, 1-hexyl-1-14C acetate, and 1-heptadecyl-1-14C acetate leads to the conclusion that the mechanism of pyrolysis of esters may be viewed as a cyclo-DEDNAN mechanism for the formation of the major alkene product and a radical mechanism for the formation of minor products.A useful synthetic procedure for the preparation of high carbon number alkenes (>10) also results from this study.

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