| Identification | More | [Name]
L-Homoserine lactone hydrochloride | [CAS]
2185-03-7 | [Synonyms]
H-L-HSE-LACTONE HCL
HOMOSERINE LACTONE HYDROCHLORIDE
HOMOSERINE(L-) LACTONE HCL
HSE LACTONE HCL
HSL
L-(-)-A-AMINO-G-BUTYROLACTONE HYDROCHLORIDE
L-(-)-HOMOSERINE LACTONE HYDROCHLORIDE
L-HOMOSERINE LACTONE HYDROCHLORIDE
(S)-2-AMINO-4-BUTYROLACTONE HYDROCHLORIDE
(S)-3-AMINO-DIHYDROFURAN-2(3H)-ONE HYDROCHLORIDE
(S)-(-)-3-AMINOTETRAHYDROFURAN-2-ONE HYDROCHLORIDE
(S)-(-)-ALPHA-AMINO-GAMMA-BUTYROLACTONE HYDROCHLORIDE
(S)-(+)-α-amino-γ-butyrolactone hydrochloride
L-Homoserine Lactone HCl
(S)-[dihydro-2-oxo-3-furyl]ammonium chloride
(S)-(-)-ALPHA-AMINO-GAMMA-BUTYROLACTON HYDROCHLORID 97%
(S)-Homoserinelactonehydrochloride
(S)-ALPHA-AMINO--BUTYROLACTONE HYDROCHLORIDE
L-Homoserine lactone hydrochloride, HSI | [EINECS(EC#)]
218-571-1 | [Molecular Formula]
C4H8ClNO2 | [MDL Number]
MFCD00058172 | [Molecular Weight]
137.56 | [MOL File]
2185-03-7.mol |
| Chemical Properties | Back Directory | [Appearance]
White Solid | [Melting point ]
210-220 °C (dec.)(lit.)
| [alpha ]
-25 º (c=0.5, water) | [refractive index ]
-26 ° (C=0.2, H2O) | [storage temp. ]
2-8°C
| [solubility ]
DMSO (Slightly), Methanol (Slightly), Water (Slightly) | [form ]
Solid | [color ]
White to Pale Beige | [biological source]
rabbit | [optical activity]
[α]20/D 27.8°, c = 1 in H2O | [Water Solubility ]
soluble | [BRN ]
3562187 | [InChIKey]
XBKCXPRYTLOQKS-DFWYDOINSA-N | [CAS DataBase Reference]
2185-03-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [F ]
3-10 | [HS Code ]
29322090 |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
(S)-α-Amino-γ-butyrolactone hydrochloride can be used:
- As a precursor for the preparation of amino-keto-alcohols and β-amino acids.
- To prepare N-acylhomoserine lactone (AHL) analogs by reacting with substituted 2-chloro-N-phenylacetamide and different halides.
- As a starting material for the synthesis of L-discadenine.
| [storage]
Store at -20°C |
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