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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

P50919-1G:
P50919-BULK:
P50919-VAR:
P50919-10G:

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.
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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
Claudio Gnaccarini et al.
Organic & biomolecular chemistry, 10(27), 5258-5265 (2012-06-02)
Transglutaminases (TGases) catalyse the transamidation of glutamine residues with primary amines. Herein we report the first FRET-based activity assay for the direct detection of the ligation (transamidation) reaction mediated by tissue TGase (TG2). This novel assay was then used in
Adrian Sulistio et al.
Chemical communications (Cambridge, England), 47(4), 1151-1153 (2010-12-15)
Highly functionalized water soluble core cross-linked star (CCS) polymers having degradable cores and hierarchical functionalities spanning from the peripheral groups along the arms to the core have been synthesized entirely from amino acid building blocks. The core-isolated moieties were shown
Anna Fodor et al.
Organic & biomolecular chemistry, 8(20), 4575-4581 (2010-08-27)
A new, heterogeneous, 4 A molecular sieve-supported copper(ii) catalyst was developed and was used successfully in the A(3) coupling of alkynes, aldehydes and amines under simple reaction conditions.
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)
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