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55699-13-3

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  • 4-tert-Butyl-2,6-dimethyl-3-hydroxyphenylacetamide(Oxymetazoline hydrochloride impurity)

    Cas No: 55699-13-3

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55699-13-3 Usage

Uses

Oxymetazoline (O876470) impurity.

Check Digit Verification of cas no

The CAS Registry Mumber 55699-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,9 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55699-13:
(7*5)+(6*5)+(5*6)+(4*9)+(3*9)+(2*1)+(1*3)=163
163 % 10 = 3
So 55699-13-3 is a valid CAS Registry Number.

55699-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 4-tert-butyl-2,6-dimethyl-3-hydroxyphenylacetamide

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:55699-13-3 SDS

55699-13-3Upstream product

55699-13-3Downstream Products

55699-13-3Relevant articles and documents

2,4,6-Trialkyl L-3-hydroxyphenylalkanoates

-

, (2008/06/13)

Ester and amides having the formula SPC1 Wherein R, R1 and R2 are independently lower alkyl or cycloalkyl groups, R3 is hydrogen, alkyl, cycloalkyl, alkylene, phenyl, phenyl substituted by alkyl groups, alkylthioethyl, thiobis-alkylene, alkyleneoxyalkylene, polyoxyalkylene or a polyvalent cyclic or acyclic hydrocarbon radical, R4 is hydrogen, lower alkyl, cycloalkyl, R5 is hydrogen, alkyl, phenyl, phenyl substituted by alkyl groups, alkylene, a polyvalent cyclic or acyclic hydrocarbon radical or alkyleneoxyalkylene, A is lower alkylene, m is 1 to 4 and n is 1 to 6. The esters are prepared by usual esterification procedures from a suitable alcohol and an acid of the formula III SPC2 or an acid halide or acid anhydride thereof. The higher alkyl esters can also be prepared from the lower alkyl ester, especially the methyl ester, by transesterification with a higher alkanol or polyol. The amides are prepared by usual amidation procedures by reacting a carboxylic acid of formula III, an acid chloride, anhydride or a lower alkyl ester thereof with the appropriate amine. The nitriles corresponding to acids of formula III are prepared as well as some malonate esters derived having the formula V. SPC3 The compounds are useful as stabilizers or organic materials, especially polyolefins, which deteriorate upon exposure to light and heat.

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