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17643-17-3

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17643-17-3 Usage

Uses

2-(2-Mercaptoethoxy)ethanol is used in preparation method of curing type hydrotreating catalyst.

Check Digit Verification of cas no

The CAS Registry Mumber 17643-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,4 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17643-17:
(7*1)+(6*7)+(5*6)+(4*4)+(3*3)+(2*1)+(1*7)=113
113 % 10 = 3
So 17643-17-3 is a valid CAS Registry Number.

17643-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Mercaptoethoxy Ethanol

1.2 Other means of identification

Product number -
Other names 1-(2-sulfanylethoxy)ethanol

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:17643-17-3 SDS

17643-17-3Relevant articles and documents

Critical role of surface hydration on the dynamics of serum adsorption studied with monoethylene glycol adlayers on gold

Avci, Ceren,Sheikh, Sonia,Blaszykowski, Christophe,Thompson, Michael

, p. 466 - 468 (2013)

The dynamics of serum adsorption on bare and monoethylene glycol adlayer-modified gold surfaces is investigated using acoustic wave physics. Hydration experiments support the pivotal role ascribed to water in the antifouling of surfaces. Behavioural discr

SELF DELIVERING BIO-LABILE PHOSPHATE PROTECTED PRO-OLIGOS FOR OLIGONUCLEOTIDE BASED THERAPEUTICS AND MEDIATING RNA INTERFERENCE

-

Page/Page column title page; 105-106, (2010/04/27)

Disclosed herein are compositions and methods for generating ribo-nucleic neutral (RNN) or deoxyribo-nucleic-neutral (DNN) polynucleotides with reduced anionic charge, for improved intracellular delivery. Also disclosed herein are methods of using RNN and DNN compositions.

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