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1,2-dimethylbutylamine, also known as DMBA, is a chemical compound belonging to the amine class of organic compounds. It is derived from butylamine, with two methyl groups attached to the first carbon in the chain. DMBA is known for its potential to increase energy levels and may promote weight loss, but its safety and legality have been questioned due to potential health risks.

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  • 35399-81-6 Structure
  • Basic information

    1. Product Name: 1,2-dimethylbutylamine
    2. Synonyms: 1,2-dimethylbutylamine;3-Methyl-2-pentanamine;Einecs 252-544-5
    3. CAS NO:35399-81-6
    4. Molecular Formula: C6H15N
    5. Molecular Weight: 101.19
    6. EINECS: 252-544-5
    7. Product Categories: N/A
    8. Mol File: 35399-81-6.mol
  • Chemical Properties

    1. Melting Point: -40.7°C (estimate)
    2. Boiling Point: 119.64°C (estimate)
    3. Flash Point: 12.7°C
    4. Appearance: /
    5. Density: 0.7500
    6. Vapor Pressure: 26.8mmHg at 25°C
    7. Refractive Index: 1.4100
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2-dimethylbutylamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2-dimethylbutylamine(35399-81-6)
    12. EPA Substance Registry System: 1,2-dimethylbutylamine(35399-81-6)
  • 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: 35399-81-6(Hazardous Substances Data)

35399-81-6 Usage

Uses

Used in Dietary Supplements and Sports Nutrition Products:
1,2-dimethylbutylamine is used as a stimulant and performance-enhancing substance for increasing energy levels and potentially promoting weight loss. However, its safety and legality have been called into question by regulatory agencies, and it has been banned in some countries. It is crucial to exercise caution and seek professional advice before using products containing 1,2-dimethylbutylamine.

Check Digit Verification of cas no

The CAS Registry Mumber 35399-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,9 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35399-81:
(7*3)+(6*5)+(5*3)+(4*9)+(3*9)+(2*8)+(1*1)=146
146 % 10 = 6
So 35399-81-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H15N/c1-4-5(2)6(3)7/h5-6H,4,7H2,1-3H3

35399-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylpentan-2-amine

1.2 Other means of identification

Product number -
Other names 1,2-Dimethylbutylamin

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:35399-81-6 SDS

35399-81-6Downstream Products

35399-81-6Relevant articles and documents

Asymmetric Amination of Secondary Alcohols by using a Redox-Neutral Two-Enzyme Cascade

Chen, Fei-Fei,Liu, You-Yan,Zheng, Gao-Wei,Xu, Jian-He

, p. 3838 - 3841 (2016/01/26)

Multienzyme cascade approaches for the synthesis of optically pure molecules from simple achiral compounds are desired. Herein, a cofactor self-sufficient cascade protocol for the asymmetric amination of racemic secondary alcohols to the corresponding chiral amines was successfully constructed by employing an alcohol dehydrogenase and a newly developed amine dehydrogenase. The compatibility and the identical cofactor dependence of the two enzymes led to an ingenious in situ cofactor recycling system in the one-pot synthesis. The artificial redox-neutral cascade process allowed the transformation of racemic secondary alcohols into enantiopure amines with considerable conversions (up to 94 %) and >99 % enantiomeric excess at the expense of only ammonia; this method thus represents a concise and efficient route for the asymmetric synthesis of chiral amines. If you know what amine: A redox-neutral two-enzyme cascade encompassing an alcohol dehydrogenase (ADH) and an amine dehydrogenase (AmDH) is constructed for the synthesis of chiral amines from the corresponding racemic alcohols in one pot to afford considerable conversions (up to 94 %) and high enantiomeric excess values (>99 %) at the expense of only ammonia.

Stereochemistry of Aliphatic Carbocations, 12. Alkyl Shifts between Secondary Carbon Atoms

Kirmse, Wolfgang,Prolingheuer, Ernst-Christoph

, p. 104 - 128 (2007/10/02)

Several optically active, β-branched alkylamines have been synthesized from amino acids.The corresponding amines were obtained from isobutyraldehyde and 2-methylbutanal (37), respectively.The stereochemistry at the terminus of 1,2-methyl shifts has been elucidated in the nitrous acid deaminations of 4 and 21.Predominant, although incomplete inversion at the migration terminus is consistent with conformational control rather than neighboring group participation.The deamination of 31 involves a degenerate 1,2-ethyl shift and a nondegenerate 1,2-methyl shift, the reverse holds for 44.Complete inversion at the origin of the methyl migrations and the absence of subsequent retrogressive H shifts strongly support the intermediacy of methyl-bridged carbocations.Partial racemization at the origin of the ethyl migrations has been traced to proton shifts within ethyl-bridged intermediates.Rearranged open cations contribute significantly to the overall reaction if micelles are produced by self-aggregation of the alkylammonium ions.

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