Prop-2-yn-1-aminium chloride
Names
[ CAS No. ]:
15430-52-1
[ 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
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
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
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...