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1-AMINO PIPERAZINE, also known as 1-Piperazinamine, is an N-aminopiperazine compound that has demonstrated significant antiviral properties. It is a heterocyclic compound with a versatile chemical structure that allows for various modifications and applications in different industries.

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  • 30651-60-6 Structure
  • Basic information

    1. Product Name: 1-AMINO PIPERAZINE
    2. Synonyms: 1-AMINO PIPERAZINE;AMINOPIPERAZINE-N;N-AMINOPIPERAZINE;1-Piperazinamine(9CI);piperazin-1-aMine
    3. CAS NO:30651-60-6
    4. Molecular Formula: C4H11N3
    5. Molecular Weight: 101.15
    6. EINECS: 625-179-8
    7. Product Categories: VARIOUSAMINE
    8. Mol File: 30651-60-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 163.1 °C at 760 mmHg
    3. Flash Point: 52.4 °C
    4. Appearance: /
    5. Density: 1 g/cm3
    6. Vapor Pressure: 2.1mmHg at 25°C
    7. Refractive Index: 1.483
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: 8.83±0.10(Predicted)
    11. CAS DataBase Reference: 1-AMINO PIPERAZINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-AMINO PIPERAZINE(30651-60-6)
    13. EPA Substance Registry System: 1-AMINO PIPERAZINE(30651-60-6)
  • Safety Data

    1. Hazard Codes: Xi
    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: 30651-60-6(Hazardous Substances Data)

30651-60-6 Usage

Uses

Used in Pharmaceutical Industry:
1-AMINO PIPERAZINE is used as an antiviral agent for its ability to exhibit antiviral activity against herpes simplex, pseudorabies, and vaccinia viruses. This makes it a promising candidate for the development of new antiviral drugs and therapies to combat these viral infections.
Used in Research and Development:
1-AMINO PIPERAZINE is used as a chemical intermediate in the synthesis of various pharmaceutical compounds, particularly those with antiviral properties. Its versatile structure allows for the development of new drugs and therapies targeting a wide range of viral diseases.
Used in Chemical Synthesis:
1-AMINO PIPERAZINE serves as a key building block in the synthesis of various organic compounds, including those with potential applications in the pharmaceutical, agrochemical, and materials science industries. Its unique structure and reactivity make it a valuable component in the development of new molecules with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 30651-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30651-60:
(7*3)+(6*0)+(5*6)+(4*5)+(3*1)+(2*6)+(1*0)=86
86 % 10 = 6
So 30651-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H11N3/c5-7-3-1-6-2-4-7/h6H,1-5H2

30651-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name piperazin-1-amine

1.2 Other means of identification

Product number -
Other names N-aminopiperazine

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:30651-60-6 SDS

30651-60-6Upstream product

30651-60-6Relevant articles and documents

Radiosynthesis and bioimaging of the tuberculosis chemotherapeutics isoniazid, rifampicin and pyrazinamide in baboons

Liu, Li,Xu, Youwen,Shea, Colleen,Fowler, Joanna S.,Hooker, Jacob M.,Tonge, Peter J.

experimental part, p. 2882 - 2891 (2010/09/14)

The front-line tuberculosis (TB) chemotherapeutics isoniazid (INH), rifampicin (RIF), and pyrazinamide (PZA) have been labeled with carbon-11 and the biodistribution of each labeled drug has been determined in baboons using positron emission tomography (P

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