Propargylamine, 98%
Propargylamine, 98%
Propargylamine, 98%
Thermo Scientific Chemicals

Propargylamine, 98%

CAS: 2450-71-7 | C3H5N | 55.08 g/mol
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Catalog NumberQuantity
ALFH53495.065 g
Catalog number ALFH53495.06
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Quantity:
5 g
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Specifications
Chemical Name or MaterialPropargylamine
CAS2450-71-7
Health Hazard 1H225-H302-H311-H314
Health Hazard 2GHS H Statement
H225-H310-H314-H318-H302
Highly flammable liquid and vapor.
Fatal in contact with skin.
Causes severe skin burns and eye damage.
Causes serious eye damage.
Harmful if swallowed.
Health Hazard 3P210-P233-P240-P241-P242-P243-P260-P264b-P270-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P370+P378q-P501c
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Propargylamine is used in the synthesis of a chiral, a fluorescent macrocycle by 1,3-dipolar cycloaddition of propargyl amides of carbohydrate-linked amino acids and 9,10-bis(azidomethyl)anthracene. It acts as an intermediate in the production of drugs.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Propargylamine is used in the synthesis of a chiral, a fluorescent macrocycle by 1,3-dipolar cycloaddition of propargyl amides of carbohydrate-linked amino acids and 9,10-bis(azidomethyl)anthracene. It acts as an intermediate in the production of drugs.

Solubility
Miscible with water, chloroform and ethyl acetate.

Notes
Hygroscopic. Light sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents and carbon dioxide.
RUO – Research Use Only

General References:

  1. He, Y.; Liang, Y.; Wang, D. The highly sensitive and facile colorimetric detection of the glycidyl azide polymer based on propargylamine functionalized gold nanoparticles using click chemistry. Chem. Commun. 2015, 51 (60), 12092-12094.
  2. Zindo, F.; Joubert, J.; Malan, S. Polycyclic propargylamine derivatives as multifunctional neuroprotective agents: cum laude. S Afr. Pharm. J. 2015, 82 (2), 32-34.