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22890-53-5

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22890-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22890-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22890-53:
(7*2)+(6*2)+(5*8)+(4*9)+(3*0)+(2*5)+(1*3)=115
115 % 10 = 5
So 22890-53-5 is a valid CAS Registry Number.

22890-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-2-hydroxybenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Et-2-OHC6H3CO2H

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:22890-53-5 SDS

22890-53-5Relevant articles and documents

Substituted amide phenol compound and its preparation method, pharmaceutical composition and use thereof

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Paragraph 0410-0413, (2019/07/04)

The invention discloses substituted-amide phenolic compounds, their preparation method, a pharmaceutical composition and an application thereof. The compounds have a structure as shown in the general formula I, wherein Z, L and Q are as defined in the spe

External preparation for skin

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, (2008/06/13)

An external preparing for skin comprising one or more than two types of 2-hydroxy benzoic acid derivative and/or salt thereof represented by the following formula: STR1 wherein R is an alkoxy group or alkyl group in the formula. The external preparation for the skin according to the present invention has a suppression effect on melanine generation by inhibition of tyrosinase activity. Accordingly, an excellent bleaching effect based upon the suppression of chromatosis and a high degree of safety can be obtained.

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