dextro,laevo-cycloserine

DL-cycloserine

CAS: 68-39-3 C3 H6 N2 O2 MW: 102.09322000

Identification

Namedextro,laevo-cycloserine
IUPAC4-amino-1,2-oxazolidin-3-one
CAS Number68-39-3
EINECS200-687-9
FDA UNIISearch
Molecular FormulaC3 H6 N2 O2
Molecular Weight102.09322000
MDL NumberMFCD00064323
Nikkaji NumberJ60.873D

Regulatory

Physical Properties

Appearance white to pale yellow crystals (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 155.00 °C. @ 760.00 mm Hg (est)
Flash Point 32.00 °F. TCC ( 0.00 °C. ) (est)
logP (o/w) -1.840 (est)
Soluble in water, 1.655e+005 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityintraperitoneal-mouse LD50 3200 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for dextro,laevo-cycloserine usage levels up tonot for fragrance use.
Recommendation for dextro,laevo-cycloserine flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

4- amino-1,2-oxazolidin-3-one 4- amino-3-isoxazolidone DL- cycloserine 3-iso xazolidinone, 4-amino- PubMed: Mechanism of synergy between epigallocatechin gallate and beta-lactams against methicillin-resistant Staphylococcus aureus. PubMed: The glutathione dependence of inorganic sulfate formation from L- or D-cysteine in isolated rat hepatocytes. PubMed: Alanine and hyperosmolarity are responsible for the stimulation of cardiomyocyte glucose transport by samples containing a glucose tolerance factor. PubMed: Inhibition of urea-cycle activity by high concentrations of alanine. PubMed: Beta-cyanoalanine synthase: purification and characterization. PubMed: [Allergic manifestations due to dl-cycloserine (oxamycin)]. PubMed: [Chemical and microbiological determination of the liberation of antitubercular agents from emulsion and suspension systems. 1. Streptomycin sulfate, rifamycin SV sodium, DL-cycloserine]. PubMed: [COMPARATIVE STUDY OF THE FUNCTIONAL AND MORPHOLOGICAL CHANGES IN THE CENTRAL NERVOUS SYSTEM OF WHITE RATS FOLLOWING INTERMITTENT ADMINISTRATION OF DL-CYCLOSERINE]. PubMed: [Comparative study of functional and morphological changes under the action of dl-cycloserine on the central nervous system]. PubMed: [Relation between dl-cycloserine and d-cycloserine and the effect on the convulsive action of various analeptics]. PubMed: Inhibition of glutamic-pyruvic transaminase by DL-cycloserine and other compounds. PubMed: [Effect of dl-cycloserine on the nervous system]. PubMed: Formation of DL-cycloserine from the methyl ester of dl-aminoxyalanine. PubMed: [Circulation of D-cycloserine & Czechosiovak DL-cycloserine in the organism]. PubMed: [Formation of dl-cycloserine from beta-hydroxaminoalanine methyl ester].