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Hexadecanoic acid, 1-(bromomethyl)-1,2-ethanediyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34607-52-8

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34607-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34607-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34607-52:
(7*3)+(6*4)+(5*6)+(4*0)+(3*7)+(2*5)+(1*2)=108
108 % 10 = 8
So 34607-52-8 is a valid CAS Registry Number.

34607-52-8SDS

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 1,2-dipalmitoylglycerol bromohydrid

1.2 Other means of identification

Product number -
Other names Dipalmitoyl-D,L-glycerin-1-bromhydrin

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:34607-52-8 SDS

34607-52-8Relevant academic research and scientific papers

Surface-Specific Cleavage of a Cationic Carbonate-Functionalized Vesicular Surfactant

Moss, Robert A.,Bhattacharya, Santanu,Scrimin, Paolo,Swarup, Shanti

, p. 5740 - 5744 (1987)

The cationic, p-nitrophenyl carbonate functionalized 1,2 -dipalmitoylglyceryl surfactant 2 was synthesized.Vesicles created at pH 3.9 from this surfactant gave rapid partial p-nitrophenol release at pH 7.9, attributed to site-specific hydrolysis of exoves

A METHOD FOR MODIFICATION OF PEPTIDES IMMOBILIZED ON A SOLID SUPPORT BY TRACELESS REDUCTIVELY CLEAVABLE LINKER MOLECULES

-

Page/Page column 55; 56, (2021/02/12)

The present invention relates to a method for modifying and purifying peptides comprising an immobilizing step, a modification step and a releasing step. In the immobilizing step, a crude linker-tagged peptide L-P is coupled to a solid support yielding an immobilized linker-tagged peptide S-L-P. Subsequently, the immobilized linker-tagged peptide S-L-P is modified with one or more organic molecules yielding an immobilized linker-tagged peptide S-L-mP. Finally, the modified peptide is released via a reduced intermediate RI. The linker molecule is a compound of formula 1, X-Tbb-Vaa-U-Y-Z (1), which can be coupled to a purification resin via the moiety X and to a peptide via the moiety Y under the release of the leaving group Z. T is an optional spacer moiety and V is an optional electron withdrawing moiety. U is an aryl or 5- or 6-membered heteroaryl moiety bound to at least one electron withdrawing moiety V, W or E. The linker is stable under acidic conditions and releases the peptide upon addition of a reducing agent.

A CONVENIENT METHOD OF ESTERIFICATION OF FATTY ACIDS. PREPARATION OF ALKYL ESTERS, STEROL ESTERS, WAX ESTERS AND TRIACYLGLYCEROLS

Saroja, M.,Kaimal, T. N. B.

, p. 1423 - 1430 (2007/10/02)

A quick and mild, one-pot method of esterification of fatty acids with pripary, secondary and tertiary alcohols as well as with fatty alcohols, sterols and glycerol is proposed via the acyl bromides formed in situ.

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