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93942-45-1

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93942-45-1 Usage

Common Use

Sunscreens and personal care products as a UV filter

Chemical Class

Triazine derivative

Function

Provides effective protection against UVB radiation

Mechanism

Absorbs and dissipates UV light

Skin Protection

Prevents damage to the skin caused by sun exposure

Safety

Considered safe for human use

Irritation

Does not cause irritation or sensitization

Popularity

Popular ingredient in sunscreen formulations

Check Digit Verification of cas no

The CAS Registry Mumber 93942-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,4 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93942-45:
(7*9)+(6*3)+(5*9)+(4*4)+(3*2)+(2*4)+(1*5)=161
161 % 10 = 1
So 93942-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H57N3/c1-7-13-16-25(10-4)19-28-22-29(20-26(11-5)17-14-8-2)24-30(23-28)21-27(12-6)18-15-9-3/h25-27H,7-24H2,1-6H3

93942-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-tris(2-ethylhexyl)-1,3,5-triazinane

1.2 Other means of identification

Product number -
Other names 1,3,5-Tri(2-ethylhexyl)hexahydro-1,3,5-triazine

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:93942-45-1 SDS

93942-45-1Downstream Products

93942-45-1Relevant articles and documents

Oligomerization catalyst

-

, (2008/06/13)

An oligomerization catalyst for olefins is obtainable from a) a chromium compound CrX3 and the at least equimolar amount, based on the chromium compound CrX3, of a ligand L or from an existing chromium complex CrX3L, in which the groups X are, independently of one another, abstractable counterions and L is a 1,3,5-triazacyclohexane of the formula I ?where the groups R1 to R9 are, independently of one another: hydrogen or organosilicon or substituted or unsubstituted carboorganic groups having from 1 to 30 carbon atoms, where two geminal or vicinal radicals R1 to R9 may also be joined to form a five—or six-membered ring, andb) at least one activating additive and also a process for preparing oligomers of olefins using these catalysts, the oligomers thus obtainable, and the oxo alcohols obtainable from these oligomers.

Synthesis of Synthetic Lubricants by Trimerization of 1-Decene and 1-Dodecene with Homogeneous Chromium Catalysts

Wasserscheid, Peter,Grimm, Siegfried,Koehn, Randolf D.,Haufe, Matthias

, p. 814 - 818 (2007/10/03)

The Cr-catalyzed trimerization of 1-decene and 1-dodecene is a highly selective method to synthesize C30 and C36 olefins. After hydrogenation, these products display very attractive viscosity indices (VI's). Due to the high trimer se

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