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P50919

Sigma-Aldrich

Propargylamine hydrochloride

95%

Synonym(s):

2-Propynylamine hydrochloride, 3-Amino-1-propyne hydrochloride

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About This Item

Linear Formula:
HC≡CCH2NH2 · HCl
CAS Number:
15430-52-1
Molecular Weight:
91.54
Beilstein:
3669858
EC Number:
239-440-5
MDL number:
MFCD00012907
UNSPSC Code:
12352100
PubChem Substance ID:
24898593
NACRES:
NA.22

Assay

95%

form

powder

reaction suitability

reaction type: click chemistry

mp

179-182 °C (lit.)

storage temp.

2-8°C

SMILES string

Cl.NCC#C

InChI

1S/C3H5N.ClH/c1-2-3-4;/h1H,3-4H2;1H

InChI key

IKXNIQJDNKPPCH-UHFFFAOYSA-N

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Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H315,H319,H335

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Thomas Hermanns et al.
Life science alliance, 3(9) (2020-07-29)
Deubiquitinating enzymes (DUBs) are important regulators of the posttranslational protein ubiquitination system. Mammalian genomes encode about 100 different DUBs, which can be grouped into seven different classes. Members of other DUB classes are found in pathogenic bacteria, which use them
Abdelouahid Samadi et al.
European journal of medicinal chemistry, 52, 251-262 (2012-04-17)
The synthesis, pharmacological evaluation and molecular modeling of heterocyclic substituted alkyl and cycloalkyl propargyl amines 1-7 of type I, and 9-12 of type II, designed as multipotent inhibitors able to simultaneously inhibit monoamine oxidases (MAO-A/B) as well as cholinesterase (AChE/BuChE)
A robust, efficient, and highly enantioselective method for synthesis of homopropargyl amines.
Erika M Vieira et al.
Angewandte Chemie (International ed. in English), 51(27), 6618-6621 (2012-05-25)
Suyan Qiu et al.
Biosensors & bioelectronics, 26(11), 4326-4330 (2011-05-21)
Copper(I) species can be acquired from the reduction of copper(II) by ascorbic acid (AA) in situ, and which in turn quantitative catalyze the azides and alkynes cycloaddition reaction. In this study, propargyl-functionalized ferrocene (propargyl-functionalized Fc) has been modified on the
Orit Bar-Am et al.
Journal of Alzheimer's disease : JAD, 21(2), 361-371 (2010-06-18)
The anti-Parkinsonian, irreversible, selective monoamine oxidase (MAO)-B inhibitors, selegiline (deprenyl, (R)-N-methyl-N-(1-phenylpropan-2-yl) prop-2-yn-1-amine) and rasagiline (Azilect, N-propargyl-1(R)-aminoindan), have been proven to possess neuroprotective/neurorestorative activities in cell cultures and animal models of neurodegenerative diseases. Structure-activity studies provide evidence that neuroprotection is associated
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