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1-Hexadecanol-1-14C is a radioactive chemical compound with the molecular formula C16H33OH, where one carbon atom is replaced by a carbon-14 isotope. 1-HEXADECANOL-1-14C is a straight-chain fatty alcohol with 16 carbon atoms, commonly used as a tracer in various biochemical and metabolic studies. It is particularly useful in research involving lipid metabolism, as it can be incorporated into cellular membranes and other lipid structures. The presence of the radioactive carbon-14 isotope allows for the tracking of the compound's distribution and metabolism within biological systems, providing valuable insights into the processes involving fatty alcohols.

3877-54-1

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3877-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3877-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3877-54:
(6*3)+(5*8)+(4*7)+(3*7)+(2*5)+(1*4)=121
121 % 10 = 1
So 3877-54-1 is a valid CAS Registry Number.

3877-54-1SDS

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 1-(14)C cetyl alcohol

1.2 Other means of identification

Product number -
Other names 1-HEXADECANOL-1-14C

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:3877-54-1 SDS

3877-54-1Upstream product

3877-54-1Downstream Products

3877-54-1Relevant academic research and scientific papers

A lysophospholipase D pathway in the metabolism of ether linked lipids in brain microsomes

Wykle,Schremmer

, p. 1742 - 1746 (2007/10/13)

Microsomal preparations from rat brain in the presence of Mg2+ hydrolyzed the ethanolamine, choline, and phosphate moieties from 1 [1 14C]hexadecyl sn glycero 3 phosphorylethanolamine, 1 [1 14C]hexadec 1 enyl sn glycero 3 phosphorylethanolamine, and 1 [1 14C]hexadecyl sn glycero 3 phosphorylcholine. Studies of the hydrolysis of 1 [1 14C]hexadecyl sn glycero 3 phosphorylethanolamine in this system indicated that the ethanolamine moiety was first removed by a phosphodiesterase to form 1 [1 14C]hexadecyl glycero 3 phosphate which was then dephosphorylated to form 1 [1 14C]hexadecylglycerol. Only minimal hydrolysis occurred when the 2 positions of the substrates were acylated; otherwise the phosphodiesterase activity was similar to that of phospholipase D from plants. The occurrence of such a lysophospholipase D pathway has not been previously reported. When Ca2+ (5 mM) was added to the system instead of Mg2+ (5 mM), little, if any, stimulation occurred; higher concentrations of Ca2+ (25 mM) inhibited the reaction. Therefore, this reaction does not appear to be related to the Ca2+ stimulated base exchange reaction found in the brain by others.

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