Sodium diethyldithiocarbamate trihydrate
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Sodium diethyldithiocarbamate trihydrate
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CAS No:
20624-25-3
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Formula:
C5H11NS2.3H2O.Na
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Chemical Name:
Sodium diethyldithiocarbamate trihydrate
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Synonyms:
Carbamodithioic acid,N,N-diethyl-,sodium salt,hydrate (1:1:3);Carbamic acid,diethyldithio-,sodium salt,trihydrate;Carbamodithioic acid,diethyl-,sodium salt,trihydrate;Sodium N,N-diethyldithiocarbamate trihydrate;Sodium diethyldithiocarbamate trihydrate;958445-96-0
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CAS No:
Description
white to light yellow crystals
A chelating agent that has been used to mobilize toxic metals from the tissues of humans and experimental animals. It is the main metabolite of DISULFIRAM.
Sodium diethyldithiocarbamate trihydrate Basic Attributes
225.31
225.046921
3920507
205-710-6
04574EXF2C
DTXSID3021275
29302000
Characteristics
39.3
1.61770
White to off-white Crystals or Powder
1.086g/cm3
95-98.5 °C(lit.)
176.4ºC at 760mmHg
60.5ºC
H2O: FREELY soluble
−20°C
5.9 (vs air)
LD50 orally in Rabbit: 1500 mg/kg LD50 dermal Rat > 1000 mg/kg
Safety Information
Ⅲ
UN 3077 9 / PGIII
3
22-38-41-36/37/38
26-39-37/39-36
EZ6550000
Xn,Xi
Stable. Incompatible with strong oxidizing agents. Hygroscopic.
P301 + P312 + P330
H302-H400
|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P310, P321, P330, P332+P313, P362, P391, and P501|Aggregated GHS information provided by 115 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)|Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. (See all compounds classified as Adjuvants, Immunologic.)|Chemicals that bind to and remove ions from solutions. Many chelating agents function through the formation of COORDINATION COMPLEXES with METALS. (See all compounds classified as Chelating Agents.)
Ammonium Salt Ditiocarb
Sodium diethyldithiocarbamate trihydrate Use and Manufacturing
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.
Computed Properties
Molecular Weight:225.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:225.04693000
Monoisotopic Mass:225.04693000
Topological Polar Surface Area:39.3
Heavy Atom Count:12
Complexity:83
Covalently-Bonded Unit Count:5
Compound Is Canonicalized:Yes
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Sodium diethyldithiocarbamate trihydrate
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