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921-04-0

N,N-Dimethyl-2-butylamine is an organic compound with the chemical formula C6H15N. It is a colorless liquid with a strong, fishy odor and is classified as a secondary amine due to the presence of two alkyl groups attached to the nitrogen atom. N,N-DIMETHYL-2-BUTYLAMINE is soluble in water and is commonly used as a solvent, a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also employed as a catalyst in various chemical reactions and as a flotation agent in the mining industry. Due to its reactive nature, N,N-dimethyl-2-butylamine should be handled with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

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  • 921-04-0 Structure

  • Basic information

    1. Product Name: N,N-DIMETHYL-2-BUTYLAMINE
    2. Synonyms: 2-(Dimethylamino)butane;2-Butanamine, N,N-dimethyl-;N,N,1-Trimethylpropylamine;N,N-Dimethyl-2-butanamine;N,N-Dimethyl-sec-butylamine;Propylamine, N,N,1-trimethyl-;sec-Butyldimethylamine;N,N-DIMETHYL-2-BUTYLAMINE
    3. CAS NO:921-04-0
    4. Molecular Formula: C6H15N
    5. Molecular Weight: 101.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 921-04-0.mol

  • Chemical Properties

    1. Melting Point: -102.35°C (estimate)
    2. Boiling Point: 93.25°C
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 0.7340
    6. Vapor Pressure: 87.1mmHg at 25°C
    7. Refractive Index: 1.4000
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N,N-DIMETHYL-2-BUTYLAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N-DIMETHYL-2-BUTYLAMINE(921-04-0)
    12. EPA Substance Registry System: N,N-DIMETHYL-2-BUTYLAMINE(921-04-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 921-04-0(Hazardous Substances Data)

921-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 921-04-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 921-04:
(5*9)+(4*2)+(3*1)+(2*0)+(1*4)=60
60 % 10 = 0
So 921-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H15N/c1-5-6(2)7(3)4/h6H,5H2,1-4H3

921-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethylbutan-2-amine

1.2 Other means of identification

Product number -
Other names sec-butyl-dimethyl-amine

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:921-04-0 SDS

921-04-0Downstream Products

921-04-0Relevant articles and documents

Ring-Opening Reactions. 31. Mechanistic Path vs. Ring Strain Control in Elimination and Substitution Reactions of 1,1-Dimethyl Cyclic Ammonium Ions and Their α,α'-Dimethyl-Substituted Derivatives

Cospito, Gabriella,Illuminati, Gabriello,Lillocci, Claudio,Petride, Horia

, p. 2944 - 2947 (2007/10/02)

From the determination of product composition and overall second-order rate constants for the reactions of a number of cyclic quaternary ammonium ions with sodium methoxide in methanol and previous similar data, a complete set of partial rate coefficients for the ring-opening reactions (substitution and elimination) of 1,1-dimethyl cyclic ammonium ions and their α,α'-dimethyl-substituted derivatives for ring sizes 4-6 was made available.Such reactions are sensitive probes for steric strain and reaction mechanism requirements in the β-elimination reaction and for thedifferent stereochemical requirements of elimination vs. substitution.

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