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2,6-dimethyl-4-morpholinepropiononitrile is a chemical compound that serves as a stabilizer in the production of polymers, particularly polyurethane foam. It is a nitrile derivative of a morpholine ring, which imparts unique chemical and physical properties to the compound. Due to its potential toxicity, it is crucial to handle this chemical with care.

84145-73-3

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84145-73-3 Usage

Uses

Used in Polymer Production Industry:
2,6-dimethyl-4-morpholinepropiononitrile is used as a stabilizer for enhancing the stability and performance of polyurethane foam. It is added to the reaction mixture to control the formation of undesirable byproducts, thereby improving the quality and safety of the final product.

Check Digit Verification of cas no

The CAS Registry Mumber 84145-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84145-73:
(7*8)+(6*4)+(5*1)+(4*4)+(3*5)+(2*7)+(1*3)=133
133 % 10 = 3
So 84145-73-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2O/c1-8-6-11(5-3-4-10)7-9(2)12-8/h8-9H,3,5-7H2,1-2H3

84145-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,6-dimethylmorpholin-4-yl)propanenitrile

1.2 Other means of identification

Product number -
Other names 4-morpholinepropanenitrile,2,6-dimethyl

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:84145-73-3 SDS

84145-73-3Relevant academic research and scientific papers

A structure-activity relationship study of novel phenylacetamides which are sodium channel blockers

Roufos, Ioannis,Hays, Sheryl,Schwarz, Roy D.

, p. 1514 - 1520 (2007/10/03)

A structure-activity relationship study of a series of novel Na+ channel blockers, structurally related to N-[3-(2,6-dimethyl-1-piperidinyl)propyl]- α-phenylbenzeneacetamide (1, PD85639) is described. The diphenylacetic acid portion of the molecule was left unchanged throughout the study, while structural features in the amine portion and the amide alkyl linkage of the molecule were modified. The compounds were tested for inhibition of veratridine-stimulated Na+ influx in CHO cells expressing type IIA Na+ channels. Several derivatives show a trend toward more potent Na+ channel blockade activity with increasing lipophilicity of the amine portion of the molecule. The presence of a phenyl ring near the amine increases inhibitory potency. A three-carbon spacer between the amide and amine is optimal, and a secondary amide linkage is preferred.

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