Product Name

  • Name

    Sodium diethyldithiocarbamate

  • EINECS 205-710-6
  • CAS No. 148-18-5
  • Article Data23
  • CAS DataBase
  • Density 1.086 g/cm3
  • Solubility water: >=10 g/100 mL at 14 °C
  • Melting Point 95 °C
  • Formula C5H10NNaS2
  • Boiling Point 176.4 °C at 760 mmHg
  • Molecular Weight 171.263
  • Flash Point 60.5 °C
  • Transport Information
  • Appearance Odorless white or slightly brown or slightly pink crystals
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 148-18-5 (Sodium diethyldithiocarbamate)
  • Hazard Symbols
  • Synonyms Sodium N,N-diethyldithiocarbamate;Carbamic acid, diethyldithio-, sodium salt;DEDC;Soxinol ESL;Diethyldithiocarbamic acid, sodium;Usaf ek-2596;DEDK;Ditiocarb sodium;Diethyldithiocarbamic acid, sodium salt;Thiocarb;GS 694A;NCI-C02835;DTC;DDC;
  • PSA 60.63000
  • LogP 1.81060

Synthetic route

carbon disulfide
75-15-0

carbon disulfide

diethylamine
109-89-7

diethylamine

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

Conditions
ConditionsYield
With sodium hydroxide In ethanol; water cooling;90%
With sodium hydroxide In ethanol at 20 - 40℃;73%
With sodium hydroxide In water at 20℃; for 1h; Cooling with ice;69%
disulfiram
97-77-8

disulfiram

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

A

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

B

C8H15NOS4
327989-09-3

C8H15NOS4

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Rate constant; Equilibrium constant; μ 0.2 mol/l;
disulfiram
97-77-8

disulfiram

sodium N,N'-diisopropyldithiocarbamate
4092-82-4

sodium N,N'-diisopropyldithiocarbamate

A

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

B

C12H24N2S4

C12H24N2S4

Conditions
ConditionsYield
With sodium nitrate; potassium hexacyanoferrate(III) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C8H15NOS4
327989-09-3

C8H15NOS4

A

bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

B

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Rate constant; Equilibrium constant; μ 0.2 mol/l;
sodium N,N'-diisopropyldithiocarbamate
4092-82-4

sodium N,N'-diisopropyldithiocarbamate

C12H24N2S4

C12H24N2S4

A

tetraisopropylothiuram disulphide
4136-91-8

tetraisopropylothiuram disulphide

B

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

Conditions
ConditionsYield
With sodium nitrate; potassium hexacyanoferrate(III) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
Tributyltin diethyldithiocarbamate
138523-63-4

Tributyltin diethyldithiocarbamate

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

Conditions
ConditionsYield
With sodium hydrogensulfide In methanol at 4℃;
concentrated NaOH

concentrated NaOH

N-(hydroxyethyl)-ethylenediamine

N-(hydroxyethyl)-ethylenediamine

Diethylene glycol monobutyl ether
112-34-5

Diethylene glycol monobutyl ether

chlorophene
120-32-1

chlorophene

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

5'-I-d(TTT)-CPG resin

5'-I-d(TTT)-CPG resin

C35H49N7O18P2S2

C35H49N7O18P2S2

Conditions
ConditionsYield
Stage #1: sodium N,N-diethyldithiocarbamate; 5'-I-d(TTT)-CPG resin In N,N-dimethyl-formamide at 20℃; for 0.0333333h;
Stage #2: With ammonium hydroxide at 60℃; for 17h;
100%
[Re(S3CPh)2(S2CPh)]

[Re(S3CPh)2(S2CPh)]

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

bis(trithioperoxybenzoato)-(diethyldithiocarbamato)rhenium (III)

bis(trithioperoxybenzoato)-(diethyldithiocarbamato)rhenium (III)

Conditions
ConditionsYield
In methanol; dichloromethane at 20℃; for 1h;100%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide
572-09-8

2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

S-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl) N,N-diethyldithiocarbamate

S-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl) N,N-diethyldithiocarbamate

Conditions
ConditionsYield
In acetone for 1h; Reflux;99%
In acetonitrile at 25℃; for 1h;63%
bis(tetraethylammonium) tri-μ2-disulfido-μ3-thio-hexabromo-triangular-trimolybdenum(IV)

bis(tetraethylammonium) tri-μ2-disulfido-μ3-thio-hexabromo-triangular-trimolybdenum(IV)

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

tris(diethyldithiocarbamato-S,S')tris(μ2-η(2)-disulfido)(μ3-sulfido)trimolybdenum(IV)(3 Mo-Mo) diethyldithiocarbamate

tris(diethyldithiocarbamato-S,S')tris(μ2-η(2)-disulfido)(μ3-sulfido)trimolybdenum(IV)(3 Mo-Mo) diethyldithiocarbamate

Conditions
ConditionsYield
In solid byproducts: Et4NBr, NaBr; mixt. was evacuated at 80 °C for 2 h, mech. activation for 1.5 h in a vac. vibration mill with steel ball (23 Hz); H2O was added, ppt. was washed with hot H2O and EtOH, dried in vac. at 75 °C, residue was treated with hot MeCN, washed with H2O and EtOH, dried in vac. at 75 °C, recrystn. from DMSO, elem. anal.;99%
[AuCl(2-thia-1,3,5-triaza-7-phosphaadamantane-2,2-dioxide)]
1243627-92-0

[AuCl(2-thia-1,3,5-triaza-7-phosphaadamantane-2,2-dioxide)]

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

[Au(diethyldithiocarbamate)(2-thia-1,3,5-triaza-7-phosphaadamantane-2,2-dioxide)]
1243628-11-6

[Au(diethyldithiocarbamate)(2-thia-1,3,5-triaza-7-phosphaadamantane-2,2-dioxide)]

Conditions
ConditionsYield
In methanol Na salt was added to suspn. of Au complex in MeOH; stirred for 18 h; filtered; washed (H2O, MeOH, Et2O); dried in air; elem. anal.;99%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

(1R,6S)-1-Methyl-7-(toluene-4-sulfonyl)-7-aza-bicyclo[4.1.0]heptane

(1R,6S)-1-Methyl-7-(toluene-4-sulfonyl)-7-aza-bicyclo[4.1.0]heptane

C19H30N2O2S3

C19H30N2O2S3

Conditions
ConditionsYield
In acetonitrile at 80℃; for 12h; stereoselective reaction;99%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

7-[(4-methylphenyl)sulfonyl]-7-azabicyclo[4.1.0]hept-3-ene
112297-29-7

7-[(4-methylphenyl)sulfonyl]-7-azabicyclo[4.1.0]hept-3-ene

C18H26N2O2S3

C18H26N2O2S3

Conditions
ConditionsYield
In acetonitrile at 80℃; for 0.5h; stereoselective reaction;99%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

2-(N-acetylanilino)-4-iodomethyl-1,3-selenazole
121995-12-8

2-(N-acetylanilino)-4-iodomethyl-1,3-selenazole

[2-(N-acetylanilino)-1,3-selenazol-4-ylmethyl]-N,N-diethyldithiocarbamate

[2-(N-acetylanilino)-1,3-selenazol-4-ylmethyl]-N,N-diethyldithiocarbamate

Conditions
ConditionsYield
In acetone for 0.5h; Heating;98%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

copper dichloride

copper dichloride

bis(N,N-diethyldithiocarbamato)copper(II)
13681-87-3

bis(N,N-diethyldithiocarbamato)copper(II)

Conditions
ConditionsYield
In neat (no solvent, solid phase) byproducts: NaCl; placing of CuCl2 and NaS2CNEt2 in 1:2 ratio to the reactor; sealing, vibrating for 60 min; sublimating in vac. at 180-190°C; crystn.; elem. anal.;98%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

tetraphenylchloroantimony(V)
16894-68-1

tetraphenylchloroantimony(V)

tetraphenylantimony N,N-diethyldithiocarbamate
109423-89-4

tetraphenylantimony N,N-diethyldithiocarbamate

Conditions
ConditionsYield
In water byproducts: NaCl; soln. of ligand in water was added to soln. of Sb-complex in water; filtered off, dried, crystd. from toluene-heptane;98%
2-(bromomethyl)-1,3-thiaselenole
1112152-67-6

2-(bromomethyl)-1,3-thiaselenole

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

(Z)-2-([(diethylamino)carbothioyl]sulfanylselanyl)ethenyl vinyl sulfide

(Z)-2-([(diethylamino)carbothioyl]sulfanylselanyl)ethenyl vinyl sulfide

Conditions
ConditionsYield
In acetonitrile at 20℃; for 0.0333333h; regioselective reaction;98%
{Mo(CPh)Br(CO)2(4-picoline)2}

{Mo(CPh)Br(CO)2(4-picoline)2}

tetraethylammonium chloride
56-34-8

tetraethylammonium chloride

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

{N(C2H5)4}(1+)*{Mo(S2CN(C2H5)2)2(CO)(C6H5CCO)}(1-)={N(C2H5)4}{Mo(S2CN(C2H5)2)2(CO)(C6H5CCO)}

{N(C2H5)4}(1+)*{Mo(S2CN(C2H5)2)2(CO)(C6H5CCO)}(1-)={N(C2H5)4}{Mo(S2CN(C2H5)2)2(CO)(C6H5CCO)}

Conditions
ConditionsYield
In tetrahydrofuran byproducts: NaBr; under inert atm.; addn. of soln. of Na-compd. to soln. of complex at -78°C, removed from cold bath and stirred at ambient temp. for 1.45 h; evapd. (vac.), dissolved in CH2Cl2, addn. of NEt4Cl, stirred for 45 min, filtered (cellulose), dried (vac., 2.5 h), treated with THF, cooled to -8°C for 30 min, supernatant decanted, , washed (THF), recrystd. (CH2Cl2/Et2O);97.5%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

zinc(II) chloride
7646-85-7

zinc(II) chloride

bis(N,N-diethyldithiocarbamato)zinc(II)
14324-55-1

bis(N,N-diethyldithiocarbamato)zinc(II)

Conditions
ConditionsYield
In neat (no solvent, solid phase) byproducts: NaCl; placing of ZnCl2 and NaS2CNEt2 in 1:2 ratio to the reactor; sealing, vibrating for 10 min; sublimating at 150-165°C in vac.; crystn.; elem. anal.;97%
dichloro(2,2'-bipyridine)platinum(II)
13965-31-6

dichloro(2,2'-bipyridine)platinum(II)

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

bis(N,N-diethyldithiocarbamate)platinum(II)
15730-38-8

bis(N,N-diethyldithiocarbamate)platinum(II)

Conditions
ConditionsYield
In not given stoich. amts., stirring for 1 h (pptn.); collection (filtration), washing (water), drying (vac.);97%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

dichlorophenylstibine
5035-52-9

dichlorophenylstibine

phenylantimony chloride diethyldithiocarbamate

phenylantimony chloride diethyldithiocarbamate

Conditions
ConditionsYield
In chloroform equimolar amts. at 25°C;97%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

dichlorophenylstibine
5035-52-9

dichlorophenylstibine

phenylantimony diethyldithiocarbamate
18615-16-2

phenylantimony diethyldithiocarbamate

Conditions
ConditionsYield
In chloroform equimolar amts. of educts at 25°C;97%
RuCl2(CO)(P(CH3)(CH(CH3)2)2)2

RuCl2(CO)(P(CH3)(CH(CH3)2)2)2

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

RuCl(CO)(S2CN(C2H5)2)(P(CH3)(CH(CH3)2)2)2

RuCl(CO)(S2CN(C2H5)2)(P(CH3)(CH(CH3)2)2)2

Conditions
ConditionsYield
In dichloromethane (inert atmosphere); stirring (12 h); filtration (Celite), solvent removal (vac.), washing (light petroleum); elem. anal.;97%
(±)-trans-N-tosyl-2-isopropyl-3-methylaziridine

(±)-trans-N-tosyl-2-isopropyl-3-methylaziridine

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

C18H30N2O2S3

C18H30N2O2S3

Conditions
ConditionsYield
In acetonitrile at 80℃; for 12h; stereoselective reaction;97%
cyclohexyl-N-tosyl aziridine
68820-12-2

cyclohexyl-N-tosyl aziridine

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

C18H28N2O2S3

C18H28N2O2S3

Conditions
ConditionsYield
In acetonitrile at 80℃; for 0.166667h; stereoselective reaction;97%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

N-tosyl-6-azabicyclo[3.1.0]hexane
81097-48-5

N-tosyl-6-azabicyclo[3.1.0]hexane

C17H26N2O2S3

C17H26N2O2S3

Conditions
ConditionsYield
In acetonitrile at 80℃; for 1h; stereoselective reaction;97%
4-Vinylbenzyl chloride
1592-20-7

4-Vinylbenzyl chloride

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

N,N-(diethylamino)dithiocarbamoylmethylstyrene

N,N-(diethylamino)dithiocarbamoylmethylstyrene

Conditions
ConditionsYield
In acetone at 40℃; for 1h;97%
bis(4-methyl-2-chloroacetamidothiazole)sulfide

bis(4-methyl-2-chloroacetamidothiazole)sulfide

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

C22H32N6O2S7

C22H32N6O2S7

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 6h;97%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

1,3,2-dioxathiane 2,2-dioxide
1073-05-8

1,3,2-dioxathiane 2,2-dioxide

C13H22NO7S3(1-)*Na(1+)

C13H22NO7S3(1-)*Na(1+)

Conditions
ConditionsYield
In methanol at 20℃;97%
4-fluoro-2-iodoaniline
61272-76-2

4-fluoro-2-iodoaniline

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

6-fluoro-N,N-diethylbenzo[d]thiazol-2-amine

6-fluoro-N,N-diethylbenzo[d]thiazol-2-amine

Conditions
ConditionsYield
With copper diacetate; potassium carbonate In N,N-dimethyl-formamide at 120℃; for 6h; Sealed tube;97%
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

cadmium(II) chloride
10108-64-2

cadmium(II) chloride

cadmium(II) diethyldithiocarbamate
14239-68-0

cadmium(II) diethyldithiocarbamate

Conditions
ConditionsYield
In neat (no solvent, solid phase) byproducts: NaCl; placing of CdCl2 and NaS2CNEt2 in 1:2 ratio to the reactor; sealing, vibrating for 60 min; sublimating in vac. at 180-230°C; crystn.; elem. anal.;96.6%
In water byproducts: NaCl; pptn. of complex from soln. at room temp., filtration while hot, drying (80°C, vac.); recrystn. (benzene); (1)H- and (13)C-NMR;
In water byproducts: NaCl; ZnCl2, the thiocarbamate in water, immediately pptn.; filtered hot to remove NaCl and any excess of unreacted thiocarbamate, dried (vac. at 80°C), recrystn. (boiling benzene);
In water solution of CdCl2 added to stirred solution of the ligand; filtered, dried, recrystd. from chloroform;
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

disulfiram
97-77-8

disulfiram

Conditions
ConditionsYield
With 1,3,5-trichloro-2,4,6-triazine; dimethyl sulfoxide In dichloromethane at 20℃; for 2h;96%
With iodine In methanol at 0℃;95%
With oxygen; sodium hydroxide In water at 25℃; for 1.08333h; pH=10; Kinetics; pH-value; Reagent/catalyst;94%
dimethyl 2-bromosuccinate
760-90-7

dimethyl 2-bromosuccinate

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

dimethyl (diethylthiocarbamoylthio)succinate
94725-95-8

dimethyl (diethylthiocarbamoylthio)succinate

Conditions
ConditionsYield
In water for 8h;96%
ethyl 2-bromoisobutyrate
600-00-0

ethyl 2-bromoisobutyrate

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

S-(1-methyl-1-ethoxycarbonylethyl) N,N-diethyl-dithiocarbamate
120924-70-1

S-(1-methyl-1-ethoxycarbonylethyl) N,N-diethyl-dithiocarbamate

Conditions
ConditionsYield
In acetone at 40℃;96%
2-chloro-1-acetoxyethane
542-58-5

2-chloro-1-acetoxyethane

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

N,N-diethyldithiocarbamic acid 2-(acetoxy)ethyl ester

N,N-diethyldithiocarbamic acid 2-(acetoxy)ethyl ester

Conditions
ConditionsYield
In acetone at 40℃;96%
With water In N,N-dimethyl-formamide at 75 - 80℃;88%
3-benzyltetrahydro-1,3-oxazine-2-thione
700840-90-0

3-benzyltetrahydro-1,3-oxazine-2-thione

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

polymer, product of cationic ring-opening polymerization, Mn 20400 Da by SEC in THF, Mn 12200 by light scattering, PDI 1.04; monomer(s): 3-benzyltetrahydro-1,3-oxazine-2-thione; sodium N,N-diethyldithiocarbamate

polymer, product of cationic ring-opening polymerization, Mn 20400 Da by SEC in THF, Mn 12200 by light scattering, PDI 1.04; monomer(s): 3-benzyltetrahydro-1,3-oxazine-2-thione; sodium N,N-diethyldithiocarbamate

Conditions
ConditionsYield
Stage #1: 3-benzyltetrahydro-1,3-oxazine-2-thione With boron trifluoride diethyl etherate In nitrobenzene at 50℃; for 24h;
Stage #2: sodium N,N-diethyldithiocarbamate In nitrobenzene; acetonitrile
96%

Sodium diethyldithiocarbamate Chemical Properties

IUPAC Name: sodium N,N-diethylcarbamodithioate
Following is the structure of Sodium diethyldithiocarbamate (CAS NO.148-18-5):
                             
Molecular formula: C5H10NNaS2 
Molecular Weight: 171.26
EINECS: 205-710-6
Melting point: 95°C 
Flash Point: 60.5 °C 
Index of Refraction: 1.555 
Molar Refractivity: 44.12 cm3
Molar Volume: 137.3 cm3
Density: 1.086 g/cm3
Surface Tension: 44.6 dyne/cm
Boiling Point: 176.4 °C at 760 mmHg
Enthalpy of Vaporization: 41.27 kJ/mol 
Vapour Pressure: 1.1 mmHg at 25 °C
Water Solubility of Sodium diethyldithiocarbamate (CAS NO.148-18-5): >=10 g/100 mL at 14 °C
Product Categories of Sodium diethyldithiocarbamate (CAS NO.148-18-5): Pharmaceutical Intermediates; Aliphatics  
Canonical SMILES: CCN(CC)C(=S)[S-].[Na+]
InChI: InChI=1S/C5H11NS2.Na/c1-3-6(4-2)5(7)8;/h3-4H2,1-2H3,(H,7,8);/q;+1/p-1
InChIKey: IOEJYZSZYUROLN-UHFFFAOYSA-M

Sodium diethyldithiocarbamate Uses

 Sodium diethyldithiocarbamate (CAS NO.148-18-5) can be used as a pesticide.

Sodium diethyldithiocarbamate Toxicity Data With Reference

1.    

oms-omi 100 µmol/L

    BBACAQ    Biochimica et Biophysica Acta. 519 (1978),65.
2.    

dnd-hmn:hla 100 µmol/L

    BBACAQ    Biochimica et Biophysica Acta. 519 (1978),65.
3.    

cyt-rat-orl 5200 mg/kg

    MUREAV    Mutation Research. 53 (1978),212.
4.    

dni-ckn:emb 4 µmol/L

    BBACAQ    Biochimica et Biophysica Acta. 519 (1978),65.
5.    

oms-ckn:emb 40 µmol/L

    BBACAQ    Biochimica et Biophysica Acta. 519 (1978),65.
6.    

orl-rat LD50:1500 mg/kg

    DRFUD4    Drugs of the Future. 6 (1981),225.
7.    

ipr-rat LD50:1250 mg/kg

    DRFUD4    Drugs of the Future. 6 (1981),225.
8.    

orl-mus LD50:1500 mg/kg

    DRFUD4    Drugs of the Future. 6 (1981),225.
9.    

ipr-mus LD50:1302 mg/kg

    DRFUD4    Drugs of the Future. 6 (1981),225.
10.    

scu-rbt LD50:500 mg/kg

    APTOA6    Acta Pharmacologica et Toxicologica. 8 (1952),329.

Sodium diethyldithiocarbamate Consensus Reports

IARC Cancer Review: Group 3 IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 7 ,1987,p. 56.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Inadequate Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 12 ,1976,p. 217.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) . NCI Carcinogenesis Bioassay (feed); No Evidence: mouse, rat NCITR*    National Cancer Institute Carcinogenesis Technical Report Series. (Bethesda, MD 20014) No. NCI-CG-TR-172 ,1979. . Reported in EPA TSCA Inventory.

Sodium diethyldithiocarbamate Safety Profile

 Moderately is toxic by ingestion, intraperitoneal, and subcutaneous routes. Experimental reproductive effects. Questionable carcinogen with experimental neoplastigenic and teratogenic data. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx, SOx, and Na2O. See also CARBAMATES.

Sodium diethyldithiocarbamate Standards and Recommendations

DFG MAK: 2 mg/m3

Sodium diethyldithiocarbamate Specification

 Sodium diethyldithiocarbamate , its cas register number is 148-18-5. It also can be called Diethyldithiocarbamic acid sodium salt ; N,N-Diethyldithiocarbamic acid, sodium salt ; and Sodium N,N-diethyldithiocarbamate . Its classification code are Agricultural Chemical; Antidote for nickel and cadmium poisoning; Fungicide, bactericide, wood preservative; Mutation data ; Reproductive Effect and Tumor data.

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