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Home > Encyclopedia > N,N-diethylcarbamodithioate

N,N-diethylcarbamodithioate

N,N-diethylcarbamodithioate structure

N,N-diethylcarbamodithioate 

structure
  • CAS No:

    392-74-5

  • Formula:

    C5H10NS2-

  • Chemical Name:

    N,N-diethylcarbamodithioate

  • Synonyms:

    Ammonium Salt Ditiocarb;Bismuth Salt Ditiocarb;Diethylcarbamodithioic Acid;Diethyldithiocarbamate;Diethyldithiocarbamate, Sodium;Diethyldithiocarbamate, Zinc;Diethyldithiocarbamic Acid;Dithiocarb;Ditiocarb;Ditiocarb Sodium;Ditiocarb, Ammonium Salt;Ditiocarb, Bismuth Salt;Ditiocarb, Lead Salt;Ditiocarb, Potassium Salt;Ditiocarb, Sodium Salt;Ditiocarb, Sodium Salt, Trihydrate;Ditiocarb, Tin(4+) Salt;Ditiocarb, Zinc Salt;Imuthiol;Lead Salt Ditiocarb;Potassium Salt Ditiocarb;Sodium Diethyldithiocarbamate;Sodium Salt Ditiocarb;Sodium, Ditiocarb;Thiocarb;Zinc Diethyldithiocarbamate;Zinc Salt Ditiocarb;Diethyldithiocarbamate;DDTC;Carbamodithioic acid, diethyl-, ion(1-);Imuthiol;Dieca;diethylcarbamodithioate;392-74-5;CHEMBL107217;Diethydithiocarbamate;Diethyldithiocarbamate ion;N,N-diethylcarbamodithioate;Diethyldithiocarbamate anion;Diethyldithiocarbamate(1-);Ba 2768;N,N-diethyldithiocarbamate;DTXSID90192448;CHEBI:144359;sodium N,N-diethyl-dithiocarbamate;BBL011325;BDBM50010231;STL146399;AKOS005206822;Carbamic acid, diethyldithio-, ion(1-);NCGC00248583-01;NCGC00248583-02;Sodium salt of Diethyl-dithiocarbamic acid(DDC);111999-EP2270005A1;111999-EP2298761A1

Description

Diethyldithiocarbamate is a member of the class of dithiocarbamate anions resulting from the removal of the proton from the dithiocarbamic acid moiety of diethyldithiocarbamic acid. It is a conjugate base of a diethyldithiocarbamic acid.|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.

N,N-diethylcarbamodithioate Basic Attributes

148.3 g/mol

148.02546667 g/mol

DTXSID90192448

Characteristics

36.3 Ų

Drug Information

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.)|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.)|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.)

Ammonium Salt Ditiocarb

Computed Properties

Molecular Weight:148.3
XLogP3:1.6
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:148.02546667
Monoisotopic Mass:148.02546667
Topological Polar Surface Area:36.3
Heavy Atom Count:8
Formal Charge:-1
Complexity:73
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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