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1,2-DIPALMITOYL-3-P-TOLUENE-SULFONYL-RAC-GLYCEROL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65266-80-0

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65266-80-0 Usage

Type

Chemical compound

Usage

Production of pharmaceuticals and cosmetics

Derivative of

Glycerol

Common use

Emulsifying agent in topical creams and ointments

Structure

Two palmitoyl (fatty acid) chains attached to the glycerol backbone

Property

Lipophilic nature

Function

Allows formation of stable emulsions

Additional group

p-Toluene-sulfonyl

Role of p-Toluene-sulfonyl group

Provides stability, control over solubility and reactivity

Known for

Improving texture and shelf-life of cosmetic and pharmaceutical products

Note

Information based on general knowledge, consult relevant expert or reference material for specific applications and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 65266-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,6 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65266-80:
(7*6)+(6*5)+(5*2)+(4*6)+(3*6)+(2*8)+(1*0)=140
140 % 10 = 0
So 65266-80-0 is a valid CAS Registry Number.

65266-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-(tosyloxy)propane-1,2-diyl dipalmitate

1.2 Other means of identification

Product number -
Other names -

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:65266-80-0 SDS

65266-80-0Downstream Products

65266-80-0Relevant academic research and scientific papers

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

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Page/Page column 56; 57, (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.

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