Substance
ID:356786
Names and Identifiers
IUPAC name
N,N-diethyl(sodiosulfanyl)carbothioamide trihydrate
Synonyms
Cupral铜锌灵二乙基二硫代氨基甲酸钠 三水合物二乙基二硫代氨基甲酸 钠盐Sodium diethyldithiocarbamate trihydrateDiethyldithiocarbamic acid sodium salt
IUPAC Traditional name
N,N-diethylsodiosulfanylcarbothioamide trihydrate
Registration numbers
CAS Number
EC Number
Beilstein Number
MDL Number
PubChem SID
Properties
Product Information
Grade
purum
Purity
≥97.0% (NT)
Linear Formula
(C2H5)2NCSSNa · 3H2O
Safety Information
Safety Statements
26-39
German water hazard class
3
Risk Statements
22-38-41
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
European Hazard Symbols
Harmful (Xn)RTECS
EZ6550000
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
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
MSDS Link
GHS Signal Word
Danger
GHS Hazard statements
H302-H315-H318
GHS Precautionary statements
P280-P305+P351+P338
Physical Property
Melting Point
95-98.5 °C(lit.)
Vapor Density
5.9 (vs air)
Molecule Details
Biochem/physiol Actions
Inhibits induction of macrophage nitric oxide synthase.
Application
Spin trap used in conjunction with Fe2+ to detect NO in brain, kidney, liver, and other tissues. Simultaneous direct measurement of NO* and pO2 has been reported. A copper chelator, it has been used to quantitate copper in biological materials by ESR and is an inhibitor of superoxide dismutase, ascorbate oxidase, and other enzymes.
Inhibits induction of macrophage nitric oxide synthase.
Application
Spin trap used in conjunction with Fe2+ to detect NO in brain, kidney, liver, and other tissues. Simultaneous direct measurement of NO* and pO2 has been reported. A copper chelator, it has been used to quantitate copper in biological materials by ESR and is an inhibitor of superoxide dismutase, ascorbate oxidase, and other enzymes.
Molecular Spectra
No Data Available
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References
No Data Available
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