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19721-22-3

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19721-22-3 Usage

Chemical Properties

Clear colorless liquid

Uses

Different sources of media describe the Uses of 19721-22-3 differently. You can refer to the following data:
1. 3-Mercapto-1-propanol is used to produce hydrophilic SAMs. Also used as a Traceless Linker for Chemical and Enzymatic Synthesis of Oligosaccharides1
2. 3-Mercapto-1-propanol has been reported to be used as a label-free capacitive DNA detection system due to it’s terminating thiol end.

Check Digit Verification of cas no

The CAS Registry Mumber 19721-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19721-22:
(7*1)+(6*9)+(5*7)+(4*2)+(3*1)+(2*2)+(1*2)=113
113 % 10 = 3
So 19721-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H8OS/c4-2-1-3-5/h4-5H,1-3H2

19721-22-3 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (405736)  3-Mercapto-1-propanol  95%

  • 19721-22-3

  • 405736-1G

  • 1,001.52CNY

  • Detail
  • Aldrich

  • (405736)  3-Mercapto-1-propanol  95%

  • 19721-22-3

  • 405736-5G

  • 2,699.19CNY

  • Detail

19721-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-MERCAPTO-1-PROPANOL

1.2 Other means of identification

Product number -
Other names 3-hydroxypropane-1-thiol

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:19721-22-3 SDS

19721-22-3Related news

Domain structure of binary self-assembled monolayers composed of 3-MERCAPTO-1-PROPANOL (cas 19721-22-3) and 1-tetradecanethiol on Au(1 1 1) prepared by coadsorption09/02/2019

The structure of the domains of phase-separated binary self-assembled monolayers (SAMs) composed of 3-mercapto-1-propanol and 1-tetradecanethiol (TDT) on Au(1 1 1) strongly depends on the thiol concentration of the solution from which the SAM is formed. Cyclic voltammograms and scanning tunnelin...detailed

Regular paperThe chemistry of 3-MERCAPTO-1-PROPANOL (cas 19721-22-3) with group 4 metallocene derivatives. The molecular structure of Cp2∗ZrCl(OCH2CH2CH2SH)09/01/2019

Titanocene or permethylzirconocene dichloride reacts with 1 molar equivalent of 3-mercapto-1-propanol (HOCH2CH2CH2SH) in the presence of NEt3 to give the monomeric chelate complex Cp2Ti(OCH2CH2CH2S) (1) or the oxygen-bonded monomeric complex Cp2∗ZrCl(OCH2CH2CH2SH) (2), respectively. When Cp2∗Zr(...detailed

Lipase-catalyzed chemospecific O-acylation of 3-MERCAPTO-1-PROPANOL (cas 19721-22-3) and 4-mercapto-1-butanol08/31/2019

The lipase-catalyzed chemospecific O-acylation of 3-mercapto-1-propanol and 4-mercapto-1-butanol by several aliphatic carboxylic acid ethyl esters are described. Similar treatment on 1-mercapto-2-propanol and 3-mercapto-2-butanol did not yield the expected O-acyl derivatives.detailed

19721-22-3Relevant articles and documents

2-mercaptoethanol synthesis

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Page/Page column 20-25, (2020/07/09)

A process comprising reacting, in a reactor having a fixed bed containing a solid catalyst which contains a zeolite, hydrogen sulfide and an oxirane in the presence of the solid catalyst to yield a reaction product with contains a mercapto-alcohol. A reactor system includes the reactor, an oxirane feed stream, a hydrogen sulfide feed stream, a fixed bed containing the solid catalyst placed inside the reactor, and an effluent stream containing the reaction product. The hydrogen sulfide and the oxirane are present in a mole ratio in a range of about 5:1 to 50:1.

PROCESS FOR PRODUCING 3-MERCAPTO-1-PROPANOL

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Page/Page column 11; 16, (2011/04/25)

3-Mercapto-1-propanol can be produced in high yield without using pyrophoric aluminum lithium hydride, by subjecting a compound of the following formula (1) to addition reaction with allyl alcohol to prepare a compound of the following formula (2) and then hydrolyzing the compound of the following formula (2) into 3-mercapto-1-propanol: wherein R1 is an alkyl group.

7-(2-AMINOETHYL) BENZOTHIAZOLONES

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, (2008/06/13)

There are disclosed compounds of formula I, Ar--CH. sub.2 CH 2--NH--CR 1 R 2--X--Y I in whichAr represents a group, STR1 X represents a C. sub.1-12 alkylene chain optionally interrupted or terminated by one or more groups selected from--S(O) n--,--O--,--C(Z)--, CR 6 R. sup.7, phenylmethyne,--NR 8--,--CONH--,--NHCO--and--NHCONH--, Y represents an optionally substituted aryl or cycloalkyl group,Z represents O or S, R 1, R 2, R 5 and R 9 each independently represent hydrogen or alkyl C 1-6,R 3 and R 4 represent hydrogen, or R. sup.3 and R 4 together form a group--S--,--NR 9--or--CH 2--,R 6 and R 7 independently represent hydrogen, alkyl C 1-6, fluoro, cyano, or CF. sub.3, provided that at least one of R 6 and R 7 is other than hydrogen,R 8 represents hydrogen or alkyl C 1-6, or when X is interrupted or terminated by more than one--NR 8--group may together with another R 8 group form the chain--CH 2--CH 2--, andn represents 0, 1 or 2,and pharmaceutically acceptable derivatives thereof.Processes for their production and pharmaceutical compositions and methods of treatment involving their use are also described.

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