structure of Allylamine hydrochloride

Allylamine hydrochloride

CAS No.: 10017-11-5
M. Wt: 93.555
M. Fa: C3H8ClN
InChI Key: MLGWTHRHHANFCC-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 10017-11-5

CAS Number

10017-11-5

EC Number

415-050-2

MDL Number

MFCD00054329

IUPAC Name

prop-2-en-1-amine;hydrochloride

InChI

InChI=1S/C3H7N.ClH/c1-2-3-4;/h2H,1,3-4H2;1H

InChIKey

MLGWTHRHHANFCC-UHFFFAOYSA-N

Canonical SMILES

C=CCN.Cl

UNII

R2H25ILF98

Physical and chemical properties of 10017-11-5

Boiling Point

54.3ºC at 760mmHg

Exact Mass

93.034531

Flash Point

>110℃

Index of Refraction

1.414

LogP

1.63340

Melting Point

106 °C

Molecular Formula

C3H8ClN

Molecular Weight

93.555

PSA

26.02000

Vapour Pressure

247mmHg at 25°C

Water Solubility

almost transparency

Safety Information of 10017-11-5

Pictograms

Signal Word

Danger

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of 10017-11-5

Allylamine hydrochloride finds use in multiple fields:

  • Polymer Science: It serves as a precursor for synthesizing poly(allylamine) and related polymers used in drug delivery systems and hydrogels.
  • Biotechnology: Its properties make it suitable for applications in cell culture and tissue engineering.
  • Chemical Industry: It is utilized in the production of surfactants, emulsifiers, and other chemical intermediates.

Interaction Studies of 10017-11-5

Research on the interactions of allylamine hydrochloride includes:

  • Binding Studies: Investigations into its ability to bind anions such as perchlorate indicate its potential use in environmental remediation technologies.
  • Cellular Interactions: Studies have demonstrated its role in enhancing cell adhesion and growth, suggesting its utility in regenerative medicine.
  • Toxicological Assessments: Evaluations of its safety profile reveal potential risks associated with skin exposure and ingestion, necessitating careful handling procedures.

Biological Activity of 10017-11-5

Allylamine hydrochloride exhibits several biological activities:

  • Antimicrobial Properties: Some studies suggest that allylamine derivatives possess antimicrobial activity against various pathogens.
  • Cell Adhesion: Poly(allylamine hydrochloride) has been investigated for its ability to promote cell adhesion and proliferation, making it a candidate for biomedical applications such as tissue engineering.
  • Toxicity: While it has beneficial properties, allylamine hydrochloride can be harmful if ingested or if it comes into contact with skin, potentially causing irritation or allergic reactions.

Physical sample testing spectrum (NMR) of 10017-11-5

Physical sample testing spectrum (NMR) of 10017-11-5

Retrosynthesis analysis of 10017-11-5

  • Route#1

    Cas:7688-51-9
    Cas:10017-11-5
  • Route#2

    Cas:20020-75-1
    Cas:10017-11-5
  • Route#3

    Cas:112-29-8
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