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About This Item
Linear Formula:
(C2H5)2NCSSNa · 3H2O
CAS Number:
Molecular Weight:
225.31
Beilstein:
3920507
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
Grade:
ACS reagent
Product Name
Sodium diethyldithiocarbamate trihydrate, ACS reagent
grade
ACS reagent
Quality Level
vapor density
5.9 (vs air)
composition
Na (as Na2SO4), 30.5-32.5%
mp
95-98.5 °C (lit.)
functional group
amine
SMILES string
[H]O[H].[H]O[H].[H]O[H].CCN(CC)C(=S)S[Na]
InChI
1S/C5H11NS2.Na.3H2O/c1-3-6(4-2)5(7)8;;;;/h3-4H2,1-2H3,(H,7,8);;3*1H2/q;+1;;;/p-1
InChI key
WWGXHTXOZKVJDN-UHFFFAOYSA-M
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General description
Sodium diethyldithiocarbamate trihydrate may be used:
- To synthesize cis-dichlorobis(N,N-diethyldithiocarbamato) tin(IV) by reacting with tin(II) chloride.
- As an alternative to xanthates to generate carbamoyl radical precursors.
- To synthesize a soluble precursor polymer for poly(thienylene vinylene).
- To synthesize dichlorotetrakis(dimethyl sulfoxide)ruthenium (II), which can be a precursor to prepare other ruthenium complexes.[17}
Application
Spin trap used in conjunction with Fe2+ to detect NO in brain, kidney, liver, and other tissues.
Spin trap used in conjunction with Fe2+ to detect NO in brain, kidney, liver, and other tissues.
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.
Biochem/physiol Actions
Inhibits induction of macrophage nitric oxide synthase.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Characterization of an unusual reaction product of tin (II) chloride with sodium N, N-diethyldithiocarbamate.
Selvaraju R, et al.
Polyhedron, 13(6), 903-908 (1994)
Incorporation of benzocarborane into conjugated polymer systems: synthesis, characterisation and optoelectronic properties.
Marshall J, et al.
Journal of Material Chemistry C, 2(2), 232-239 (2014)
Precursor route poly (thienylene vinylene) for organic solar cells: Photophysics and photovoltaic performance
Gunes S, et al.
Solar Energy Materials and Solar Cells, 90(17), 2815-2828 (2006)
Dithiocarbamate Group Transfer Cyclization Reactions of Carbamoyl Radicals under ?Tin?Free? Conditions
Grainger RS and Innocenti P
Angewandte Chemie (International Edition in English), 43(26), 3445-3448 (2004)
Anna M Biesbrock et al.
Journal of visualized experiments : JoVE, (91)(91), 51953-51953 (2014-10-07)
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