L-homoserine lactone hydrochloride

Modify Date: 2024-01-04 16:17:15

L-homoserine lactone hydrochloride Structure
L-homoserine lactone hydrochloride structure
Common Name L-homoserine lactone hydrochloride
CAS Number 2185-03-7 Molecular Weight 137.56
Density N/A Boiling Point 257.1ºC at 760 mmHg
Molecular Formula C4H8ClNO2 Melting Point 221-226ºC
MSDS Chinese USA Flash Point 120.1ºC
Symbol GHS07
GHS07
Signal Word Warning

 Use of L-homoserine lactone hydrochloride


L-Homoserine lactone hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name (3S)-3-aminooxolan-2-one,hydrochloride
Synonym More Synonyms

 L-homoserine lactone hydrochloride Biological Activity

Description L-Homoserine lactone hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
References

[1]. Koch, T., and Buchardt, O.Synthesis of L-(+)-selenomethionineSynthesis1065-1067(1993)

[2]. Chhabra, SR, Harty, C., Hooi, DSW, et al.Synthetic analogues of the bacterial signal (quorum seeing) molecule N-(3-oxododecanoyl)-L-homoserine lactone as immune modulators J. Med. Chem. 46(1) 97-104(2003)

 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

 Safety Information

Symbol GHS07
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

 Customs

HS Code 2932209090
Summary 2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles28

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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)

 Synonyms

(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)
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