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119313-12-1

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119313-12-1 Usage

Chemical Properties

Light yellow solid

Uses

Different sources of media describe the Uses of 119313-12-1 differently. You can refer to the following data:
1. DBMP can be used as a dopant to dope silicone elastomer for the formation of 3D biocompatible scaffolds. It can also be used in two photon polymerization for the micro-fabrication of 3D hydrogels for potential biomedical and tissue engineering applications.
2. UV solidify ink and coating

General Description

2-Benzyl-2-(dimethylamino)-4′-morpholinobutyrophenone (DBMP) is a photoinitiator that acts at near UV and visible range. It can be incorporated into the polymeric matrix, which upon UV irradiation forms radicals by radical chain polymerization.

Check Digit Verification of cas no

The CAS Registry Mumber 119313-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,1 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119313-12:
(8*1)+(7*1)+(6*9)+(5*3)+(4*1)+(3*3)+(2*1)+(1*2)=101
101 % 10 = 1
So 119313-12-1 is a valid CAS Registry Number.

119313-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Benzyl-2-(dimethylamino)-4'-morpholinobutyrophenone

1.2 Other means of identification

Product number -
Other names 2-Benzyl-2-dimethylamino-1-(4-morpholinophenyl)-1-butanone

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:119313-12-1 SDS

119313-12-1Relevant articles and documents

A 1 - (4 - morpholino phenyl) -1 - butanone preparation method

-

, (2019/05/16)

The invention relates to a kind of α - amino ethyl ketone photoinitiator intermediate preparation method, in particular to photoinitiator 2 - benzyl - 2 - dimethylamino - 1 - (4 - morpholino phenyl) butanone and 2 - (4 - methyl benzyl) - 2 - dimethylamino - 1 - (4 - morpholino phenyl) butanone intermediate 1 - (4 - morpholino-phenyl) - 1 - butanone. To overcome the shortcomings of the prior art, provides a does not need to add the heavy metal catalyst, does not need high-temperature high-pressure feeding, after treatment is simple, the appearance of the product is good, is suitable for the industrial production of α - amino ethyl ketone photoinitiator preparation method of the midbody.

Alpha-amino acetophenone photoinitiator preparation method

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, (2016/10/07)

The present invention relates to an alpha-amino acetophenone photoinitiator preparation method, particularly to a preparation method of 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)butanone and 2-(4-methylbenzyl)-2-dimethylamino-1-(4-morpholinophenyl)butanone. According to the present invention, 1-p-fluorophenyl-1-butanone is adopted as the raw material, and only the safe and cheap solvent is used in the whole method to conveniently prepare 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)butanone and 2-(4-methylbenzyl)-2-dimethylamino-1-(4-morpholinophenyl)butanone; and the method has characteristics of cheap and readily available raw materials, high yield, no requirement of intermediate purification, and continuous reaction without solvent replacement, and is the preparation method with characteristics of low cost, environmental protection and easy operation and suitable for industrialization.

Novel nitrogen-containing titanocenes, and the use thereof

-

, (2008/06/13)

Titanocenes of the formula I STR1 in which R1 are cyclopentadienyl? groups and R2 and R3 are aromatic radicals which are substituted in both ortho-positions by fluorine and, in addition, are substituted by a pyrrylalkyl group, amidoalkyl group or imidoalkyl group, are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds.

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