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6010-34-0

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6010-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6010-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6010-34:
(6*6)+(5*0)+(4*1)+(3*0)+(2*3)+(1*4)=50
50 % 10 = 0
So 6010-34-0 is a valid CAS Registry Number.

6010-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]phenol

1.2 Other means of identification

Product number -
Other names Ionox 312

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:6010-34-0 SDS

6010-34-0Downstream Products

6010-34-0Relevant articles and documents

2-(2′-hydroxyphenyl)benzotriazoles used as U.V. stabilizers

-

, (2008/06/13)

2-(2′-hydroxyphenyl)benzotriazoles having general formula (I). The above 2-(2′-hydroxyphenyl)benzotriazoles are useful as light stabilizers for organic polymers.

2-(2'Hydroxyphenyl) benzotriazoles and process for their preparation

-

, (2008/06/13)

2-(2'-hydroxyphenyl)benzotriazoles having general formula (I): The above 2-(2'-hydroxyphenyl)benzotriazoles can be used as light stabilizers for organic polymers.

SUBSTITUTED DIALKYLAMINOMETHYLPHENOLS IN AN EXCHANGE REACTION WITH CARBOXYLIC ACID ANHYDRIDES

Nikiforov, G. A.,Bannikov, G. F.,Mal'donado, I. K. A. Romero,Malysheva, R. D.,Ershov, V. V.

, p. 2530 - 2535 (2007/10/02)

Carboxylic acid benzyl esters are formed in the reaction of carboxylic acid anhydrides with N,N-dialkyl-4(2)-hydroxy-substituted benzylamines. 4-Hydroxy-3,5-di-tert-butylbenzyl acetate exchanges an acetyl fragment for an alkoxyl fragment and benzylates phenol derivatives in the presence of an acid.

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