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45584-07-4

4-AMINO-1-METHYLPIPERIDINE, with the molecular formula C6H14N2, is a piperidine derivative characterized by a piperidine ring with a methyl group attached to the nitrogen atom and an amino group at the 4th carbon position. This versatile chemical compound serves as a crucial intermediate in the synthesis of a wide range of pharmaceuticals, agrochemicals, and other organic compounds. It is also utilized as a building block in the production of various drugs and active pharmaceutical ingredients, showcasing its importance in both industrial and scientific applications.

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  • 45584-07-4 Structure

  • Basic information

    1. Product Name: 4-AMINO-1-METHYLPIPERIDINE
    2. Synonyms: 1-METHYL-PIPERIDIN-4-YLAMINE;4-AMINO-N-METHYLPIPERIDINE;4-AMINO-1-METHYL PIPERIDNE;AKOS BBS-00005327;AKOS B016064;ART-CHEM-BB B016064;CHEMBRDG-BB 4003460;TIMTEC-BB SBB004306
    3. CAS NO:45584-07-4
    4. Molecular Formula: C6H14N2
    5. Molecular Weight: 114.19
    6. EINECS: 921-218-0
    7. Product Categories: Piperidine
    8. Mol File: 45584-07-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 62-64°C 1mm
    3. Flash Point: 52.228 °C
    4. Appearance: /
    5. Density: 0.912 g/cm3
    6. Vapor Pressure: 1.778mmHg at 25°C
    7. Refractive Index: 1.472
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.40±0.20(Predicted)
    11. CAS DataBase Reference: 4-AMINO-1-METHYLPIPERIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-AMINO-1-METHYLPIPERIDINE(45584-07-4)
    13. EPA Substance Registry System: 4-AMINO-1-METHYLPIPERIDINE(45584-07-4)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 36/37/38-41-37/38-22
    3. Safety Statements: 26-36/37/39-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 45584-07-4(Hazardous Substances Data)

45584-07-4 Usage

Uses

Used in Pharmaceutical Industry:
4-AMINO-1-METHYLPIPERIDINE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and active pharmaceutical ingredients. Its unique structure allows for the creation of diverse compounds with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-AMINO-1-METHYLPIPERIDINE is employed as a precursor in the production of agrochemicals, aiding in the development of effective and environmentally friendly solutions for pest control and crop protection.
Used in Organic Compounds Synthesis:
4-AMINO-1-METHYLPIPERIDINE is used as a building block in the synthesis of a variety of organic compounds, enabling the creation of novel chemical entities with potential applications in various industries.
Used in Research and Development:
4-AMINO-1-METHYLPIPERIDINE is utilized in research and development for the synthesis of novel compounds with biological activity, driving scientific innovation and the discovery of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 45584-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,5,8 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 45584-07:
(7*4)+(6*5)+(5*5)+(4*8)+(3*4)+(2*0)+(1*7)=134
134 % 10 = 4
So 45584-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-7-6-2-4-8-5-3-6/h6-8H,2-5H2,1H3

45584-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methylpiperidin-4-amine

1.2 Other means of identification

Product number -
Other names N-methylpiperidin-4-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:45584-07-4 SDS

45584-07-4Relevant articles and documents

The effect of substitution on the utility of piperidines and octahydroindoles for reversible hydrogen storage

Cui, Yi,Kwok, Samantha,Bucholtz, Andrew,Davis, Boyd,Whitney, Ralph A.,Jessop, Philip G.

, p. 1027 - 1037 (2008/12/20)

Substituted piperidines and octahydroindoles are compared in terms of their usability as reversible organic hydrogen storage liquids for hydrogen-powered fuel cells. Theoretical Gaussian calculations indicate which structural features are likely to lower the enthalpy of dehydrogenation. Experimental results show that attaching electron donating or conjugated substituents to the piperidine ring greatly increases the rate of catalytic dehydrogenation, with the greatest rates being observed with 4-aminopiperidine and piperidine-4-carboxamide. Undesired side reactions were observed with some compounds such as alkyl transfer reactions during the dehydrogenation of 4-dimethylaminopiperidine, C-O and C-N cleavage reactions during hydrogenation and/or subsequent dehydrogenation of 4-alkoxy and 4-amino indoles, and disproportionation during the hydrogenation of 4-aminopyridine. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

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