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N-Methyl Diisobutylamine, with the molecular formula C10H23N, is a tertiary amine characterized by a bulky isobutyl group and a methyl group attached to the nitrogen atom. This colorless, water-insoluble liquid possesses a strong amine odor and is recognized for its flammability and hazardous nature if not handled with care.

10471-20-2

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10471-20-2 Usage

Uses

Used in Chemical Catalysts:
N-Methyl Diisobutylamine is utilized as a catalyst in various chemical reactions, enhancing the rate of these processes and improving overall efficiency.
Used in Pesticide Production:
In the agricultural industry, N-Methyl Diisobutylamine serves as an intermediate in the synthesis of pesticides, contributing to the development of effective solutions for pest control.
Used in Rubber Chemicals:
N-METHYL DIISOBUTYLAMINE is employed as an intermediate in the production of rubber chemicals, which are essential for the manufacturing of rubber products with enhanced properties.
Used in Pharmaceutical Industry:
N-Methyl Diisobutylamine plays a crucial role as an intermediate in the synthesis of various pharmaceuticals, aiding in the development of new drugs and medications.
Used as a Corrosion Inhibitor:
In industrial applications, N-Methyl Diisobutylamine functions as a corrosion inhibitor, protecting metal surfaces from degradation and extending their lifespan.
Used in Fuel and Lubricant Additives:
N-METHYL DIISOBUTYLAMINE is also used as an additive in fuel and lubricants, improving their performance and reducing wear on engines and machinery.

Check Digit Verification of cas no

The CAS Registry Mumber 10471-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10471-20:
(7*1)+(6*0)+(5*4)+(4*7)+(3*1)+(2*2)+(1*0)=62
62 % 10 = 2
So 10471-20-2 is a valid CAS Registry Number.

10471-20-2SDS

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 N,2-dimethyl-N-(2-methylpropyl)propan-1-amine

1.2 Other means of identification

Product number -
Other names Diisobutylmethylamin

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:10471-20-2 SDS

10471-20-2Downstream Products

10471-20-2Relevant academic research and scientific papers

Method for selectively preparing N-monomethylamine compound

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Paragraph 0034-0035, (2017/08/29)

The invention discloses a method for selectively preparing an N-monomethylamine compound. The method takes an amine compound, formaldehyde and H2 as reaction raw materials; the raw materials react in a reaction medium in the presence of a compound catalyst at 30 DEG C-180 DEG C for 2h-48h, so as to obtain the N-monomethylamine compound; and the compound catalyst is composed of oxides of at least two of the following metal or oxides of least one of the following metal and at least one metal simple substance: aluminum, copper, nickel, cobalt and iron. According to the method for preparing the N-monomethylamine compound, the conversion ratio and the selectivity of N-monomethylamine are relatively high; the H2 is used as a reducing agent and is clean, cheap and environment-friendly; the catalyst utilized by the method is cheap, simple to prepare and high in catalysis efficiency; and the method has mild preparation and reaction conditions and the catalyst has no corrosiveness, is easy to separate and can be repeatedly used.

The Chemistry of N-Substituted Benzotriazoles. Part 14. Novel Routes to Secondary and Tertiary Amines and to N,N-Disubstituted Hydroxylamines

Katritzky, Alan R.,Yannakopoulou, Konstantina,Lue, Ping,Rasala, Danuta,Urogdi, Laszlo

, p. 225 - 233 (2007/10/02)

Tertiary amines of types R4R3CHNR1R2 (2), (R2CH2)2NR1 (10) and 11, or (R2CH2)3N (12), secondary amines of type (R2CH2)2NH (8), and N,N-disubstituted hydroxylamines of type (R2CH2)2NOH (9), are prepared in high yield by the action of Grignard reagents or sodium borohydride on easily available N,N-dialkyl-N-amines (1) or tris(benzotriazolylmethyl)amine (7), on bis(benzotriazolylmethyl)amines (3), (5), and (6), and on N,N-bis(benzotriazolylmethyl)hydroxylamine (4), respectively.

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