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OCTYL 3-MERCAPTOPROPIONATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71849-93-9

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71849-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71849-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,4 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71849-93:
(7*7)+(6*1)+(5*8)+(4*4)+(3*9)+(2*9)+(1*3)=159
159 % 10 = 9
So 71849-93-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H22OS/c1-3-5-6-7-8-9-10-13-11(12)4-2/h3-10H2,1-2H3

71849-93-9SDS

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 octyl 3-sulfanylpropanoate

1.2 Other means of identification

Product number -
Other names Octyl 3-mercaptopropionate

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:71849-93-9 SDS

71849-93-9Downstream Products

71849-93-9Relevant academic research and scientific papers

Macrocyclic derivative and assemblies formed therefrom

-

Page/Page column 21, (2014/10/16)

The present invention is directed to a macrocyclic derivative which is formed by modification of a macrocycle. The invention further relates to assemblies formed by the self-assembly of such macrocyclic derivatives in aqueous solvent, and includes bilayer vesicles, micelles, monolayers, nanoparticles, colloidal assemblies and surface-coated assemblies.

Poly-6-cationic amphiphilic cyclodextrins designed for gene delivery

Byrne, Colin,Sallas, Florence,Rai, Dilip K.,Ogier, Julien,Darcy, Raphael

experimental part, p. 3763 - 3771 (2009/10/23)

A new series of amphiphilic cyclodextrins containing cationic groups at the 6-positions and alkyl or biolabile ester groups at the 2-positions has been synthesised. Selective 2-O-allylation followed by photochemical addition of lipophilic thiols made it possible to control lipophilicity in these mesomolecules and allow solubility and self-assembly in water. The cationic groups are cysteamine-derived, while the alkyl and ester groups are C 1-C16 and benzyl ester groups. This is a new general synthetic route to a potentially wide range of polycationic cyclodextrins capable of acting as gene delivery vectors by condensing DNA and forming liquid crystalline complexes with oligonucleotides.

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