(S)-(-)-1,2-Diaminopropane dihydrochloride
Suppliers
Names
[ CAS No. ]:
19777-66-3
[ Name ]:
(S)-(-)-1,2-Diaminopropane dihydrochloride
[Synonym ]:
(S)-(−)-Propylenediamine dihydrochloride
(2S)-propane-1,2-diamine dihydrochloride
1,2-Propanediamine, (2S)-, hydrochloride (1:2)
(S)-diaminopropane dihydrochloride
(S)-(-)-Diaminopropane Hydrochloride
S-(-)-1,2-diaminopropane dihydrochloride
R-(-)-1,2-propanediamine dihydrochloride
(S)-1,2-diaminopropane
(S)-1,2-propanediamine*2HCl
(S)-1,2-Diaminopropane Dihydrochloride
(2S)-1,2-Propanediamine dihydrochloride
(S|)-1,2-Propanediamine dihydrochloride
(S)-Propane-1,2-diamine dihydrochloride
(S)-1,2-Propanediamine dihydrochloride
(S)-1,2-Diaminopropane 2HCl
MFCD01862631
(S)-Propylenediamine Dihydrochloride
(S)-(-)-1,2-Diaminopropane dihydrochloride
Chemical & Physical Properties
[ Boiling Point ]:
215.8ºC at 760 mmHg
[ Melting Point ]:
227-229ºC
[ Molecular Formula ]:
C3H12Cl2N2
[ Molecular Weight ]:
147.047
[ Flash Point ]:
84.3ºC
[ Exact Mass ]:
146.037750
[ PSA ]:
52.04000
[ LogP ]:
2.29690
[ Vapour Pressure ]:
0.12mmHg at 25°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
2811.0
[ WGK Germany ]:
3
[ Hazard Class ]:
6.1
[ HS Code ]:
2921290000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2921290000
[ Summary ]:
2921290000 other acyclic polyamines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%
Articles
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 873(1) , 15-9, (2008)
Capillary gas chromatographic (GC) determination of methylglyoxal (MGo) was developed on the basis of precolumn derivatization with 1,2-diaminopropane (DAP) at pH 3. The elution was carried out on an ...
J. Med. Chem. 23 , 1232, (1980)
The synthesis and alpha-adrenergic blocking activity of a series of optically active 2,4-disubstituted imidazolines are presented. The substituted analogues of naphazoline, tolazoline, and clonidine p...
J. Med. Chem. 19 , 1382, (1976)
The synthesis of (R)-(+)-4-methyl-2-(1-naphthylmethyl)imidazoline hydrochloride (2) and (S)-(-)-4-methyl-2-(1-naphthylmethyl)imidazoline hydrochloride (3) is presented. The synthesis involves the prep...