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108098-37-9

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108098-37-9 Usage

Chemical composition

Consists of a phenol group with a hexylamino methyl substituent.

Molar mass

207.31 g/mol.

Usage

Commonly used as an antiseptic and disinfectant.

Efficacy

Effective against a wide range of bacteria and fungi.

Applications

Used in medical and personal care products, as well as in industrial settings for controlling microbial growth and preserving goods.

Safety precautions

Can be toxic and irritating to the skin, eyes, and respiratory system, so it should be handled and used with care.

Check Digit Verification of cas no

The CAS Registry Mumber 108098-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,9 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108098-37:
(8*1)+(7*0)+(6*8)+(5*0)+(4*9)+(3*8)+(2*3)+(1*7)=129
129 % 10 = 9
So 108098-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H21NO/c1-2-3-4-7-10-14-11-12-8-5-6-9-13(12)15/h5-6,8-9,14-15H,2-4,7,10-11H2,1H3

108098-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(hexylamino)methyl]phenol

1.2 Other means of identification

Product number -
Other names N-Hexyl-2-hydroxy-benzylamin

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:108098-37-9 SDS

108098-37-9Downstream Products

108098-37-9Relevant articles and documents

Structure - bacteriostatic activity relationship for 2-aminomethylphenols and their ammonium salts

Kudryavtseva,Molodykh,Ryzhkina,Shagidullina,Timofeeva,Bel'skii

, p. 194 - 198 (2007/10/03)

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A FACILE SYNTHESIS OF HOGHLY FUNCTIONALIZED UNSYMMETRICAL HETEROBIARYLS UTILIZING THE INTRAMOLECULAR ULLMANN COUPLING REACTION DIRECTED BY SALICYL ALCOHOL AS A TEMPLATE

Takahashi, Masami,Kuroda, Tooru,Ogiku, Tsuyoshi,Ohmizu, Hiroshi,Kondo, Kazuhiko,Iwasaki, Tameo

, p. 1867 - 1882 (2007/10/02)

The cyclic heterobiaryls (3) containing a thenoyl of furoyl group were synthesized in good yields by regioselective acylations of salicyl alcohol (1), followed by the intramolecular Ullmann coupling reaction of the diesters (2).The cleavage of the two est

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