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55543-68-5

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55543-68-5 Usage

General Description

Crezacin is a chemical compound that is commonly used in the pharmaceutical industry. It is primarily used as an ingredient in topical ointments and creams due to its anti-inflammatory and anti-fungal properties. Crezacin is known for its ability to reduce redness, itching, and swelling caused by various skin conditions such as eczema, psoriasis, and dermatitis. It is also used as a preservative in some cosmetic products. Additionally, crezacin may have potential applications in the treatment of certain types of cancer due to its anti-proliferative effects. Overall, crezacin is a versatile chemical that is valued for its numerous medical and cosmetic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 55543-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,4 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55543-68:
(7*5)+(6*5)+(5*5)+(4*4)+(3*3)+(2*6)+(1*8)=135
135 % 10 = 5
So 55543-68-5 is a valid CAS Registry Number.

55543-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[bis(2-hydroxyethyl)amino]ethanol,2-(2-methylphenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names T 2M

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:55543-68-5 SDS

55543-68-5Relevant articles and documents

New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium

Adamovich,Oborina,Ushakov,Mirskova

, p. 2227 - 2229 (2018/12/11)

Physiologically and pharmacologically active het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium of pharmacopeial purity have been synthesized by the reaction of het(aryl)chalcogenylacetic acids with sodium (potassium) hydroxide and triethanolami

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