Substance
ID:182282
Names and Identifiers
Synonyms
N-Acetyl-3-(nitrosothio)-DL-valineS-Nitroso-N-acetylpenicillamineSNAPS-Nitroso-N-acetyl-DL-penicillamine
IUPAC name
2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid
IUPAC Traditional name
2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid
Properties
Safety Information
Safety Statements
26-36
GHS Precautionary statements
P261-P305+P351+P338
Risk Statements
36/37/38
Storage Temperature
-20°C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
European Hazard Symbols
Irritant (Xi)GHS Signal Word
Warning
GHS Hazard statements
H315-H319-H335
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
German water hazard class
3
Physical Property
Solubility
H2O: ≥2 mg/mL
DMSO: ≥20 mg/mL, clear, light green
Apperance
green powder
Product Information
Purity
≥97%
Quality Level
PREMIUM
Molecule Details
Biochem/physiol Actions
NO donor; vasodilator, smooth muscle relaxant, lymphocyte activator. Activates soluble guanylyl cyclase.
SNAP, a nitrosothiol derivative, releases nitric oxide (NO.) under physiological conditions thus making it a useful tool for studying pharmacological and physiological actions of NO. Because of its NO releasing properties SNAP is a potent vasodilator in vitro and in vivo and is less prone to produce pharmacological tolerance.
NO donor; vasodilator, smooth muscle relaxant, lymphocyte activator. Activates soluble guanylyl cyclase.
SNAP, a nitrosothiol derivative, releases nitric oxide (NO.) under physiological conditions thus making it a useful tool for studying pharmacological and physiological actions of NO. Because of its NO releasing properties SNAP is a potent vasodilator in vitro and in vivo and is less prone to produce pharmacological tolerance.
Molecular Spectra
No Data Available
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References
No Data Available
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