L-homoserine lactone hydrochloride
Suppliers
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)
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...
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...
Mikrobiologiia 82(2) , 147-56, (2013)