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6920-24-7

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6920-24-7 Usage

Chemical Properties

beige powder

Uses

1,2-Hexadecanediol was used as reducing agent in the preparation of silver nanocrystals from a dichlorobenzene solution containing oleyl amine as a surfactant. It was also used in the preparation of:Au-Fe3O4 hetero-dimersiron pyrite nanocrystalsmonodisperse iron platinum nanoparticles

Definition

ChEBI: A glycol that is hexadecane which is substituted by hydroxy groups at positions 1 and 2.

Check Digit Verification of cas no

The CAS Registry Mumber 6920-24-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6920-24:
(6*6)+(5*9)+(4*2)+(3*0)+(2*2)+(1*4)=97
97 % 10 = 7
So 6920-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16(18)15-17/h16-18H,2-15H2,1H3

6920-24-7 Well-known Company Product Price

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  • Aldrich

  • (213748)  1,2-Hexadecanediol  technical grade, 90%

  • 6920-24-7

  • 213748-50G

  • 4,148.82CNY

  • Detail

6920-24-7SDS

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 1,2-hexadecanediol

1.2 Other means of identification

Product number -
Other names 1,2-Hexadecanediol

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:6920-24-7 SDS

6920-24-7Relevant articles and documents

-

Weiss

, p. 1576 (1965)

-

Ring opening of a fatty epoxide by diethylacetamido malonate in basic medium by phase transfer catalysis or under microwave irradiation

Abenhaim,Loupy,Mahieu,Semeria

, p. 1809 - 1816 (1994)

A fatty epoxide (tetradecyl-oxirane) is reacted with diethyl acetamidomalonate in basic medium, with or without solvent under solid-liquid phase transfer catalysis with LiCl, or under microwave irradiation on supported reagents (KF/Al2O3/LiCl). The main product is a lactone which is formed after epoxide ring opening and subsequent cyclisation. We put here into evidence, for the first time, the conjugated advantages of 'dry media' reactions, lithium salt effects and microwave irradiation.

Total synthesis of (-)-goniotrionin

Dias, Luiz C.,Ferreira, Marco A. B.

experimental part, p. 4046 - 4062 (2012/06/29)

A stereoselective total synthesis of the reported structure of goniotrionin (4) has been accomplished. The key steps involved the opening of a chiral epoxide, a highly diastereoselective Mukaiyama aerobic oxidative cyclization, a selective 1,2-syn Mukaiyama aldol reaction, and a Noyori reduction.

DERMATOLOGICAL COMPOSITIONS AND METHODS

-

, (2008/06/13)

Disclosed are methods and compositions for regulating the melanin content of mammalian melanocytes; regulating pigmentation in mammalian skin, hair, wool or fur; treating or preventing various skin and proliferative disorders; by administration of various compounds, including alcohols, diols and/or triols and their analogues.

Treatment of diseases mediated by the nitric oxide/cGMP/protein kinase G pathway

-

, (2008/06/13)

Disclosed are methods and compositions for stimulating cellular nitric oxide (NO) synthesis, cyclic guanosine monophosphate levels (cGMP), and protein kinase G (PKG) activity for purposes of treating diseases mediated by deficiencies in the NO/cGMP/PKG signal transduction pathway, by administration of various compounds including alcohols, diols and/or triols and their analogues.

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