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1,2,3-triphenylbutan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6333-99-9

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6333-99-9 Usage

Physical state

White crystalline solid

Uses

a. Fragrance ingredient
b. Production of lotions, soaps, and cosmetics
c. Photoinitiator in adhesives and inks

Medicinal properties

Inhibits growth of certain cancer cells

Potential health concerns

Classified as a potential endocrine disruptor

Adverse health effects

Linked to adverse health effects in some studies

Ongoing research

Debate regarding safety and potential regulation

Check Digit Verification of cas no

The CAS Registry Mumber 6333-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6333-99:
(6*6)+(5*3)+(4*3)+(3*3)+(2*9)+(1*9)=99
99 % 10 = 9
So 6333-99-9 is a valid CAS Registry Number.

6333-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-triphenylbutan-1-one

1.2 Other means of identification

Product number -
Other names 1-Butanone,1,2,3-triphenyl

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:6333-99-9 SDS

6333-99-9Relevant academic research and scientific papers

Epimerization and Kinetic Protonation as Factors Determining the Stereochemistry of the Michael Reaction

Gospodova, Tzveta S.,Stefanovsky, Yuri N.

, p. 275 - 280 (2007/10/02)

Model compounds in which the only possibility for isomerization is epimerization were synthesized.They undergo isomerization under the conditions widely used in the Michael addition.Conclusions are drawn as to the possibilities for epimerization or kineti

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