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Sodium diethyldithiocarbamate trihydrate

ACS reagent, for the determination and separation of heavy metals, ≥99.0%

Synonym(s):

Cupral, Diethyldithiocarbamic acid sodium salt

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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:
12000000
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor density

5.9 (vs air)

Assay

≥99.0%

form

powder

quality

for the determination and separation of heavy metals

mp

95-98.5 °C (lit.)

cation traces

Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
Mn: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

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 is a chelating agent, generally used in mobilizing toxic metals from the human tissues and experimental animals. It exists as a white or colorless solid, and is freely soluble with gradual decomposition.

Application

Sodium diethyldithiocarbamate trihydrate was used during the synthesis of N-allylpeptides, in a study outlining the strategy to synthesize and purify a hydrogen bond surrogate (HBS) α-helix in ∼1 week.
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.

Other Notes

Reagent used for the extraction of trace metals into organic solvents for atomic absorption spectroscopy; Precipitation of trace metals for x-ray fluorescence spectroscopy

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard 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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Inhibition of induction of benzpyrene hydroxylase by nickel carbonyl.
Sunderman, F. William.
Cancer Research, 27.5, 950-955 (1967)
K.L. Cheng et al.
Handbook of Organic Analytical Reagents (1982)
S. Bruggerhoff et al.
Fresenius Journal of Analytical Chemistry, 311, 252-252 (1982)
W. Klemm et al.
Fresenius Journal of Analytical Chemistry, 364, 429-429 (1999)
Paul A. Bouis
Reagent Chemicals: Specifications and Procedures, 609-609 (2006)

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