Substance
ID:355082
Names and Identifiers
Synonyms
L-Canavanine sulfate saltL-刀豆氨酸 硫酸盐4-胍氧丁胺酸 硫酸盐L-α-Amino-γ-(guanidinooxy)butyric acid sulfate salt
IUPAC Traditional name
canavanine; sulfuric acid
IUPAC name
(2S)-2-amino-4-(carbamimidamidooxy)butanoic acid; sulfuric acid
Registration numbers
Beilstein Number
EC Number
CAS Number
MDL Number
PubChem SID
Properties
Product Information
Empirical Formula (Hill Notation)
C5H12N4O3 · H2SO4
Purity
≥98.0% (TLC)
Safety Information
Risk Statements
20/21/22
European Hazard Symbols
Harmful (Xn)Storage Temperature
2-8°C
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Hazard statements
H302-H312-H332
GHS Precautionary statements
P280
MSDS Link
Safety Statements
36
German water hazard class
3
GHS Signal Word
Warning
Physical Property
Optical Rotation
[α]20/D +17±1°, c = 2% in H2O
Melting Point
160-165 °C (dec.)
Molecule Details
Other Notes
A structural analog of L-arginine. Review: Biological effects and mode of action1
Biochem/physiol Actions
Naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity with this L-amino acid. It is a selective inhibitor of inducible nitric oxide synthase (iNOS).
A structural analog of L-arginine. Review: Biological effects and mode of action1
Biochem/physiol Actions
Naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity with this L-amino acid. It is a selective inhibitor of inducible nitric oxide synthase (iNOS).
Molecular Spectra
No Data Available
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References
No Data Available
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