L-homoserine lactone hydrochloride
Names
[ CAS No. ]:
2185-03-7
[ Name ]:
L-homoserine lactone hydrochloride
[Synonym ]:
(S)-α-Amino-γ-butyrolactone hydrochloride
(S)-(-)-α-Amino-γ-butyrolactone Hydrochloride
2(3H)-Furanone, 3-aminodihydro-, (3S)-, hydrochloride (1:1)
(S)-3-Aminodihydrofuran-2(3H)-one hydrochloride
(S)-(-)-3-Aminotetrahydrofuran-2-one Hydrochloride
(3S)-3-Aminodihydrofuran-2(3H)-one hydrochloride (1:1)
(S)-(+)-|A-amino-|A-butyrolactone hydrochloride
L-(-)-Homoserine Lactone Hydrochloride
EINECS 218-571-1
L-Homoserine lactone hydrochloride
L-Homoserine lactone HCl
(2S)-homoserine lactone hydrochloride
LSHLO,HCl
(S)-Homoserine-lactone hydrochloride
MFCD00058172
(3S)-3-Aminodihydro-2(3H)-furanone hydrochloride (1:1)
Biological Activity
[Description]:
[Related Catalog]:
[References]
Chemical & Physical Properties
[ Boiling Point ]:
257.1ºC at 760 mmHg
[ Melting Point ]:
221-226ºC
[ Molecular Formula ]:
C4H8ClNO2
[ Molecular Weight ]:
137.56
[ Flash Point ]:
120.1ºC
[ Exact Mass ]:
137.024353
[ PSA ]:
52.32000
[ LogP ]:
0.76290
[ Vapour Pressure ]:
0.000411mmHg at 25°C
[ Index of Refraction ]:
-26 ° (C=0.2, H2O)
[ Storage condition ]:
2~8°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-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2932209090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2932209090
[ Summary ]:
2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Psychol. Bull. 141(2) , 404-46, (2015)
Among immigrant Asian and Latino groups, the contrast between collectivism in traditional heritage and individualism in the mainstream American cultures presents unique challenges for their family rel...
Catalytic asymmetric construction of spiro(γ-butyrolactam-γ-butyrolactone) moieties through sequential reactions of cyclic imino esters with Morita-Baylis-Hillman bromides.Chemistry 18(40) , 12614-8, (2012)
Spiro(γ-butyrolactam-γ-butyrolactone): a route to enantioenriched spiro(γ-butyrolactam-γ-butyrolactone) compounds, a valuable motif for drug discovery, was developed by use of a highly efficient coppe...
[The influence of bacterial autoregulation molecules (homoserine lactones and alkyloxybenzoles) on oxidative metabolism of the natural immunity cellular effectors].Mikrobiologiia 82(2) , 147-56, (2013)