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339-72-0

339-72-0 Structure

339-72-0 Structure
IdentificationMore
[Name]

L-CYCLOSERINE
[CAS]

339-72-0
[Synonyms]

H-CYCLOSERINE
L-4-AMINO-3-ISOOXAZOLIDINONE
L-4-AMINO-3-ISOXALOLIDINONE
L-4-AMINO-3-ISOXAZOLIDINONE
L-CYCLOSERINE
S(-)-4-AMINO-3-ISOXAZOLIDINONE
(S)-4-AMINO-3-ISOXAZOLIDONE
(l)-3-isoxazolidinon
(s)-3-isoxazolidinon
Levcycloserine
L-4-aminoisoxazolidin-3-one
(S)-(-)-CYCLOSERINE, 97%
L-CYCLOSERIN
3-Isoxazolidinone, 4-amino-, (4S)-
3-Isoxazolidinone, 4-amino-, (S)-
Cyclo-L-serine
3-Isoxazolidinone,4-amino-,(4S)-(9CI)
(S)-4-Amino-3-isoxazolidone, L-4-Amino-3-isoxazolidinone, L-Cycloserine, L-cycloserine
(4S)-4-Aminoisoxazolidin-3-one
(S)-4-Aminoisoxazolidin-3-one
[EINECS(EC#)]

206-427-0
[Molecular Formula]

C3H6N2O2
[MDL Number]

MFCD00064324
[Molecular Weight]

102.09
[MOL File]

339-72-0.mol
Chemical PropertiesBack Directory
[Appearance]

WHITE GRANULAR POWDER
[Melting point ]

147 °C
[Boiling point ]

191.38°C (rough estimate)
[density ]

1.278
[refractive index ]

1.5110 (estimate)
[storage temp. ]

2-8°C
[solubility ]

H2O: soluble50mg/mg protein
[form ]

White to off-white powder.
[pka]

14.36±0.40(Predicted)
[color ]

White to Off-White
[Water Solubility ]

H2O: 50mg/mg protein
[BRN ]

80799
[CAS DataBase Reference]

339-72-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R5:Heating may cause an explosion.
R20:Harmful by inhalation.
[Safety Statements ]

S38:In case of insufficient ventilation, wear suitable respiratory equipment .
S36/37:Wear suitable protective clothing and gloves .
[WGK Germany ]

2
[RTECS ]

NY2976000
[F ]

10
Hazard InformationBack Directory
[Chemical Properties]

WHITE GRANULAR POWDER
[Uses]

antibacterial, coccidiostat
[Uses]

L-Cycloserine is an irreversible inhibitor of 3-ketodihydrosphingosine synthetase.
[Definition]

ChEBI: A 4-amino-1,2-oxazolidin-3-one that has S configuration. An antibiotic isolated from Erwinia uredovora.
[Biochem/physiol Actions]

L-cycloserine is a potent inhibitor of serine palmitoyltransferase, the first step of sphingolipid synthesis.
[Purification Methods]

Purify cycloserine by recrystallisation from aqueous EtOH or MeOH or aqueous NH3/EtOH or isoPrOH. Also recrystallise it from aqueous ammoniacal solution at pH 10.5 (100mg/mL) by diluting with 5 volumes of isopropanol and then adjusting to pH 6 with acetic acid. An aqueous solution, buffered to pH 10 with Na2CO3, can be stored in a refrigerator for 1week without decomposition. UV: max at 226nm (A1cm 1% 4.02). The tartrate salt has m 165-166o (dec), 166-168o (dec), and [] D 24 -41o (c 0.7, H2O). [Stammer et al. J Am Chem Soc 79 3236 1959, UV: Kuehl J Am Chem Soc 77 2344 1955, Beilstein 27 III/IV 5549.]
Spectrum DetailBack Directory
[Spectrum Detail]

L-CYCLOSERINE(339-72-0)FT-IR
L-CYCLOSERINE(339-72-0)Raman
L-CYCLOSERINE(339-72-0)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

L-Cycloserine, 99%(339-72-0)
[Sigma Aldrich]

339-72-0(sigmaaldrich)
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