Prop-2-yn-1-aminium chloride

Names

[ Name ]:
Prop-2-yn-1-aminium chloride

[Synonym ]:
2-Propyn-1-amine, hydrochloride (1:1)
2-Propyn-1-amine hydrochloride (1:1)
Prop-2-yn-1-amine hydrochloride (1:1)
PropargylaMine Hydrochloride
Prop-2-yn-1-amine hydrochloride
3-Amino-1-propyne Hydrochloride
prop-2-yn-1-amine,hydrochloride
Prop-2-yn-1-aminium chloride
MFCD00041601
EINECS 239-440-5
Propynylamine Hydrochloride

Chemical & Physical Properties

[ Density]:
0.989 g/mL at 25 °C(lit.)

[ Boiling Point ]:
27-28 °C(lit.)

[ Melting Point ]:
179-182 °C(lit.)

[ Molecular Formula ]:
C₃H₆ClN

[ Molecular Weight ]:
91.539

[ Flash Point ]:
91 °F

[ Exact Mass ]:
91.018875

[ PSA ]:
26.02000

[ LogP ]:
1.08060

[ Vapour Pressure ]:
76.8mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.417(lit.)

[ Storage condition ]:
0-6°C

[ Stability ]:
Moisture SensitiveHighly Toxic

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H315-H319-H335

[ Precautionary Statements ]:
P261-P301 + P310-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges

[ Hazard Codes ]:
T:Toxic;

[ Risk Phrases ]:
R25;R36/37/38

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 2811 6.1/PG 2

[ WGK Germany ]:
3

[ RTECS ]:
UK5076000

[ Packaging Group ]:
II

[ Hazard Class ]:
6.1

[ HS Code ]:
2921199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2921199090

[ Summary ]:
2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Monoclonal antibody-functionalized multilayered particles: targeting cancer cells in the presence of protein coronas.

ACS Nano 9(3) , 2876-85, (2015)

Engineered particles adsorb biomolecules (e.g., proteins) when introduced in a biological medium to form a layer called a "corona". Coronas, in particular the protein corona, play an important role in...

Stereoselective intermolecular C-H amination reactions.

Chem. Commun. (Camb.) 48(63) , 7799-801, (2012)

A novel chiral N-mesyloxycarbamate to perform rhodium-catalyzed stereoselective C-H amination reactions is reported. Chiral benzylic and propargylic amines are produced in good yields and selectivitie...

Kinetic resolution of propargylamines via a highly enantioselective non-enzymatic N-acylation process.

Chem. Commun. (Camb.) 48(85) , 10511-3, (2012)

The non-enzymatic kinetic resolution of diversely substituted primary propargylic amines is reported featuring a highly selective acetyl transfer using (1S,2S)- in conjunction with Aliquat(TM) 336, af...