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38256-93-8

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38256-93-8 Usage

Description

N-(2-Methoxyethyl)methylamine, with the chemical formula C4H11NO, is an organic chemical compound that exists as a clear, colorless liquid. It has a faint, amine-like odor and is widely recognized for its utility as a building block in the synthesis of various chemical products.

Uses

Used in Pharmaceutical Industry:
N-(2-Methoxyethyl)methylamine is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new medications due to its reactive amine group which can form amide and other types of bonds essential in drug structures.
Used in Agrochemical Industry:
In the agrochemical sector, N-(2-Methoxyethyl)methylamine serves as a building block for the synthesis of agrochemicals, playing a role in the creation of pesticides and other agricultural products that are vital for crop protection and yield enhancement.
Used in Solvent Applications:
N-(2-METHOXYETHYL)METHYLAMINE is also utilized as a solvent in various chemical processes, capitalizing on its ability to dissolve a range of substances, which is beneficial for numerous industrial applications.
Used in Surfactant and Detergent Production:
N-(2-Methoxyethyl)methylamine is employed as an intermediate in the production of surfactants and detergents, where it aids in creating compounds that reduce the surface tension of liquids, thus improving the effectiveness of cleaning products.
Safety and Handling:
Given its classification as a hazardous substance, N-(2-Methoxyethyl)methylamine necessitates careful handling to prevent irritation to the skin, eyes, and respiratory system. It is crucial to store and manage this compound in a well-ventilated area and to employ suitable personal protective equipment to mitigate potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 38256-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,5 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38256-93:
(7*3)+(6*8)+(5*2)+(4*5)+(3*6)+(2*9)+(1*3)=138
138 % 10 = 8
So 38256-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H11NO/c1-5-3-4-6-2/h5H,3-4H2,1-2H3

38256-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-METHOXYETHYL)METHYLAMINE

1.2 Other means of identification

Product number -
Other names N-(2-Methoxyethyl)methylamine

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:38256-93-8 SDS

38256-93-8Relevant articles and documents

Benzothiazole derivatives with activity as adenosine receptor ligands

-

, (2008/06/13)

The present invention relates to substituted benzothiazole derivitives and to their pharmaceutically acceptable salts useful for the treatment of diseases related to the adenosine receptor.

Schiff's Bases as Intermediates in the Hydrolytic Decomposition of 2-Alkyl-3-methyl-1,3-oxazolidines in Aqueous Acid

Pihlaja, Kalevi,Parkkinen, Aija,Loennberg, Harri

, p. 1223 - 1226 (2007/10/02)

The kinetics for the hydrolysis of 2-alkyl-3-methyl-1,3-oxazolidines have been examined spectrophotometrically in acidic solutions.The decomposition of the substrates to 2-methylaminoethanol and the corresponding aldehydes have been shown to proceed via stable intermediates which are kinetically and u.v.-spectroscopically very similar to the acyclic cationic Schiff's base derived from isobutyraldehyde and 2-methoxyethylmethylamine.The mechanisms for the formation and breakdown of the Schiff's base intermediate are discussed on the basis of pH-rate profiles, activation parameters, salt effects, and solvent deuterium isotope effects.

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