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131215-92-4

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131215-92-4 Usage

Uses

9-MNL can be used in the surface modification of gold electrodes for the fabrication of biosensors for biomedical applications.

General Description

9-Mercapto-1-nonanol (9-MNL) is an alkanethiol that forms a self-assembled monolayer (SAM) on a variety of substrates. It facilitates the immobilization of the surface atoms.

Check Digit Verification of cas no

The CAS Registry Mumber 131215-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131215-92:
(8*1)+(7*3)+(6*1)+(5*2)+(4*1)+(3*5)+(2*9)+(1*2)=84
84 % 10 = 4
So 131215-92-4 is a valid CAS Registry Number.

131215-92-4 Well-known Company Product Price

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  • Aldrich

  • (698768)  9-Mercapto-1-nonanol  96%

  • 131215-92-4

  • 698768-1G

  • 714.87CNY

  • Detail

131215-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-sulfanylnonan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Nonanol,9-mercapto

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:131215-92-4 SDS

131215-92-4Upstream product

131215-92-4Downstream Products

131215-92-4Relevant articles and documents

Rational size control of gold nanoparticles employing an organometallic precursor [Au-C≡C-t-Bu]4 and tunable thiolate-functionalized ionic liquids in organic medium

Luska, Kylie L.,Moores, Audrey

scheme or table, p. 145 - 152 (2012/03/07)

Gold nanoparticles (Au NPs) stabilized with six different thiolate-functionalized ionic liquids (TFILs) were synthesized in an organic solvent. The size and optical properties of the TFIL-stabilized Au NPs can be rationally controlled by altering the N-alkyl chain length and (or) the counteranion of the TFIL-stabilizing ligand. Au NPs were prepared from the reduction of a gold precursor (HAuCl4 or [Au-C≡C-t-Bu] 4) employing NaBH4 in the presence of the different disulfide precursors. A model, based on Israelachvili theory, is proposed to account for the dependence of NP size on the N-alkyl chain length and the counteranion of the surfactantlike TFIL stabilizers.

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