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N-methyl-3,5-dichlorobenzylamine is a chemical compound characterized by the molecular formula C9H10Cl2N. It is a derivative of benzylamine, featuring two chlorine atoms at the 3 and 5 positions on the benzene ring and a methyl group attached to the amine nitrogen. N-methyl-3,5-dichlorobenzylamine is recognized for its potent antibacterial properties, which make it a valuable asset in the realm of sanitation and hygiene.

90390-21-9

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90390-21-9 Usage

Uses

Used in Household and Industrial Cleaning Products:
N-methyl-3,5-dichlorobenzylamine is utilized as a disinfectant and antimicrobial agent in various cleaning products. Its strong antibacterial properties allow it to effectively eliminate a broad spectrum of bacteria, fungi, and viruses, ensuring a hygienic and clean environment.
Used in Healthcare Settings:
In the healthcare industry, N-methyl-3,5-dichlorobenzylamine is employed for disinfection and sterilization purposes. Its effectiveness against a wide range of pathogens makes it a crucial component in maintaining a sterile environment, thus preventing the spread of infections and promoting patient safety.
Used in Sanitation and Hygiene Applications:
Beyond household and industrial cleaning, N-methyl-3,5-dichlorobenzylamine is also applied in broader sanitation and hygiene applications. Its versatility in combating various microorganisms makes it a commonly used chemical for ensuring cleanliness and reducing the risk of disease transmission in various settings.

Check Digit Verification of cas no

The CAS Registry Mumber 90390-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,9 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90390-21:
(7*9)+(6*0)+(5*3)+(4*9)+(3*0)+(2*2)+(1*1)=119
119 % 10 = 9
So 90390-21-9 is a valid CAS Registry Number.

90390-21-9SDS

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 3,5-Dichloro-N-methylbenzylamine

1.2 Other means of identification

Product number -
Other names 1-(3,5-dichlorophenyl)-N-methylmethanamine

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:90390-21-9 SDS

90390-21-9Downstream Products

90390-21-9Relevant academic research and scientific papers

Tertiary Amine Pyrazolones and Their Salts as Inhibitors of Mutant Superoxide Dismutase 1-Dependent Protein Aggregation for the Treatment of Amyotrophic Lateral Sclerosis

Zhang, Yinan,Zhao, Kevin Tianmeng,Fox, Susan G.,Kim, Jinho,Kirsch, Donald R.,Ferrante, Robert J.,Morimoto, Richard I.,Silverman, Richard B.

, p. 5942 - 5949 (2015/08/24)

Pyrazolone derivatives have previously been found to be inhibitors of Cu/Zn superoxide dismutase 1 (SOD1)-dependent protein aggregation, which extended survival of an amyotrophic lateral sclerosis (ALS) mouse model. On the basis of ADME analysis, we describe herein a new series of tertiary amine-containing pyrazolones and their structure-activity relationships. Further conversion to the conjugate salts greatly improved their solubility. Phosphate compound 17 exhibited numerous benefits both to cellular activity and to CNS-related drug-like properties in vitro and in vivo, including microsomal stability, tolerated toxicity, and blood-brain barrier permeation. These results indicate that tertiary amine pyrazolones comprise a valuable class of ALS drug candidates.

TACHYKININ RECEPTOR ANTAGONISTS

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Page 29, (2010/02/10)

The present invention relates to selective NK-1 receptor antagonists of Formula (I) or a pharmaceutically acceptable salt thereof, for the treatment of disorders associated with an excess of tachykinins.

Benzylamines: Synthesis and evaluation of antimycobacterial properties

Meindl,Von Angerer,Schonenberger,Ruckdeschel

, p. 1111 - 1118 (2007/10/02)

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

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