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93216-90-1

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93216-90-1 Usage

Common uses

Illicit production of methylenedioxymethamphetamine (MDMA), also known as ecstasy

Physical properties

Colorless liquid with a strong odor

Hazard class

Highly flammable, classified as a hazardous chemical

Health and environmental risks

Potential to cause harm to human health and the environment

Legal status

Controlled substance in many countries, regulated and monitored by law enforcement agencies to prevent illegal manufacturing and trafficking of illicit drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 93216-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,1 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93216-90:
(7*9)+(6*3)+(5*2)+(4*1)+(3*6)+(2*9)+(1*0)=131
131 % 10 = 1
So 93216-90-1 is a valid CAS Registry Number.

93216-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)-2-methyl-2-morpholin-4-ylpropan-1-one

1.2 Other means of identification

Product number -
Other names p-methoxy-2,2-dimethyl-2-N-morpholinoacetophenone

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:93216-90-1 SDS

93216-90-1Upstream product

93216-90-1Relevant articles and documents

Aminoaryl ketone photoinitiators

-

, (2008/06/13)

The photopolymerizable mixture described contains (A) at least one ethylenically unsaturated photopolymerisable compound, (B) a photoinitiator of the formula I STR1 and (C) a photosensitiser from the group of aromatic carbonyl compounds having a triplet energy of 225-310 kJ/mol, for example xanthones, thioxianthones, coumarins, phthalimides, phenones and the like. Ar is phenyl substituted in the 4-position by a substituted amino group, R1 and R2 are alkyl, R3 and R4 are alkyl or alkoxyalkyl, or R3 and R4 together are 3-oxapentamethylene. Said sensitisers (C) raise the activity of said photoinitiators (B) without shortening the shelf life of the mixtures. The photocurable mixtures are used especially as binders for printing inks or paints.

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