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21436-52-2

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21436-52-2 Usage

Description

1-BROMOHEXADECAN-2-ONE, also known as BHT-Keto Bromo, is a chemical compound that belongs to the class of organobromides. It is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
1-BROMOHEXADECAN-2-ONE is used as an intermediate for the synthesis of pharmaceuticals, contributing to the development of various medications.
Used in Agrochemical Industry:
1-BROMOHEXADECAN-2-ONE is used as an intermediate for the synthesis of agrochemicals, aiding in the production of agricultural products.
Used in Organic Chemical Reactions:
1-BROMOHEXADECAN-2-ONE is used as a reagent in organic chemical reactions, facilitating various chemical processes.
Used in Fragrance and Flavor Production:
1-BROMOHEXADECAN-2-ONE is used as a starting material for the production of fragrances and flavors, enhancing the sensory qualities of various products.
Safety Precautions:
It is important to handle 1-Bromoheptadecan-2-one with caution, as it is classified as a hazardous substance and can cause irritation to the skin, eyes, and respiratory system. The chemical should be stored and handled following proper safety measures to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 21436-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,3 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21436-52:
(7*2)+(6*1)+(5*4)+(4*3)+(3*6)+(2*5)+(1*2)=82
82 % 10 = 2
So 21436-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H31BrO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16(18)15-17/h2-15H2,1H3

21436-52-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H27872)  1-Bromo-2-hexadecanone, 97%   

  • 21436-52-2

  • 10g

  • 1136.0CNY

  • Detail
  • Alfa Aesar

  • (H27872)  1-Bromo-2-hexadecanone, 97%   

  • 21436-52-2

  • 50g

  • 3488.0CNY

  • Detail

21436-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromohexadecan-2-one

1.2 Other means of identification

Product number -
Other names 1-Bromo-2-hexadecanone

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:21436-52-2 SDS

21436-52-2Downstream Products

21436-52-2Relevant articles and documents

Acylcarnitine analogues as topical, microbicidal spermicides.

Savle, Prashant S.,Doncel, Gustavo F.,Bryant, Stephen D.,Hubieki, M. Patricia,Robinette, R. Graham,Gandour, Richard D.

, p. 2545 - 2548 (1999)

Acylcarnitine analogues, (+)-6-Carboxylatomethyl-2-alkyl-4,4-dimethylmorpholinium (Z-n, where n = the number of carbons in the alkyl chain), synthesized in multi-gram quantities show in vitro activities as spermicides, anti-HIV agents, and inhibitors of the growth of Candida albicans. Activity improves with increasing chain length. Compound Z-15 is a candidate for further study as a topical, microbicidal spermicide.

3-O-Alkylascorbic Acids as Free-Radical Quenchers: Synthesis and Inhibitory Effect on Lipid Peroxidation

Nihro, Yasunori,Miyataka, Hideki,Sudo, Tadamitsu,Matsumoto, Hitoshi,Satoh, Toshio

, p. 2152 - 2157 (2007/10/02)

A novel series of 3-O-alkylascorbic acids (3-RASA, 3a-n) was synthesized to act as radical scavengers for active oxygen species and free radicals, and their redox potential and inhibitory effects on lipid peroxidation in rat liver microsomes were evaluated.The redox potentials of the 3-RASA compounds were increased by the substituent group to 90-190 mV above the potential for ascorbic acid (i.e., 3-RASA compounds were harder to oxidize).Although 3-O-dodecylascorbic acid (3c) and 3-O-(decylcarbomethyl)ascorbic acid (3i) differed in their redox potentials, they both markedly inhibited lipid peroxidation in rat liver microsomes to a similar extent (IC50 = 3.1 and 3.3E-6M, respectively).Structure-activity relationship studies demonstrated that the anti lipid peroxidation activity of the 3-RASA compounds was markedly dependent upon their hydrophobicity.

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