Conditions | Yield |
---|---|
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
sodium O-ethyl dithiocarbonate
A
sodium N,N-diethyldithiocarbamate
B
C8H15NOS4
Conditions | Yield |
---|---|
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Rate constant; Equilibrium constant; μ 0.2 mol/l; |
disulfiram
sodium N,N'-diisopropyldithiocarbamate
A
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
With sodium nitrate; potassium hexacyanoferrate(III) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l; |
sodium O-ethyl dithiocarbonate
C8H15NOS4
A
bis-ethoxythiocarbonyldisulfane
B
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
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
A
tetraisopropylothiuram disulphide
B
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
With sodium nitrate; potassium hexacyanoferrate(III) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l; |
Tributyltin diethyldithiocarbamate
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
With sodium hydrogensulfide In methanol at 4℃; |
BPA
Diethylene glycol monobutyl ether
chlorophene
sodium N,N-diethyldithiocarbamate
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
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% |
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
In methanol; dichloromethane at 20℃; for 1h; | 100% |
sodium N,N-diethyldithiocarbamate
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide
Conditions | Yield |
---|---|
In acetone for 1h; Reflux; | 99% |
In acetonitrile at 25℃; for 1h; | 63% |
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
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)]
sodium N,N-diethyldithiocarbamate
[Au(diethyldithiocarbamate)(2-thia-1,3,5-triaza-7-phosphaadamantane-2,2-dioxide)]
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 12h; stereoselective reaction; | 99% |
sodium N,N-diethyldithiocarbamate
7-[(4-methylphenyl)sulfonyl]-7-azabicyclo[4.1.0]hept-3-ene
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 0.5h; stereoselective reaction; | 99% |
sodium N,N-diethyldithiocarbamate
2-(N-acetylanilino)-4-iodomethyl-1,3-selenazole
Conditions | Yield |
---|---|
In acetone for 0.5h; Heating; | 98% |
sodium N,N-diethyldithiocarbamate
bis(N,N-diethyldithiocarbamato)copper(II)
Conditions | Yield |
---|---|
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
tetraphenylchloroantimony(V)
tetraphenylantimony N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
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
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 0.0333333h; regioselective reaction; | 98% |
Conditions | Yield |
---|---|
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
zinc(II) chloride
bis(N,N-diethyldithiocarbamato)zinc(II)
Conditions | Yield |
---|---|
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)
sodium N,N-diethyldithiocarbamate
bis(N,N-diethyldithiocarbamate)platinum(II)
Conditions | Yield |
---|---|
In not given stoich. amts., stirring for 1 h (pptn.); collection (filtration), washing (water), drying (vac.); | 97% |
Conditions | Yield |
---|---|
In chloroform equimolar amts. at 25°C; | 97% |
sodium N,N-diethyldithiocarbamate
dichlorophenylstibine
phenylantimony diethyldithiocarbamate
Conditions | Yield |
---|---|
In chloroform equimolar amts. of educts at 25°C; | 97% |
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
In dichloromethane (inert atmosphere); stirring (12 h); filtration (Celite), solvent removal (vac.), washing (light petroleum); elem. anal.; | 97% |
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 12h; stereoselective reaction; | 97% |
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 0.166667h; stereoselective reaction; | 97% |
sodium N,N-diethyldithiocarbamate
N-tosyl-6-azabicyclo[3.1.0]hexane
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 1h; stereoselective reaction; | 97% |
Conditions | Yield |
---|---|
In acetone at 40℃; for 1h; | 97% |
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 6h; | 97% |
Conditions | Yield |
---|---|
In methanol at 20℃; | 97% |
4-fluoro-2-iodoaniline
sodium N,N-diethyldithiocarbamate
Conditions | Yield |
---|---|
With copper diacetate; potassium carbonate In N,N-dimethyl-formamide at 120℃; for 6h; Sealed tube; | 97% |
sodium N,N-diethyldithiocarbamate
cadmium(II) chloride
cadmium(II) diethyldithiocarbamate
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
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
sodium N,N-diethyldithiocarbamate
dimethyl (diethylthiocarbamoylthio)succinate
Conditions | Yield |
---|---|
In water for 8h; | 96% |
ethyl 2-bromoisobutyrate
sodium N,N-diethyldithiocarbamate
S-(1-methyl-1-ethoxycarbonylethyl) N,N-diethyl-dithiocarbamate
Conditions | Yield |
---|---|
In acetone at 40℃; | 96% |
Conditions | Yield |
---|---|
In acetone at 40℃; | 96% |
With water In N,N-dimethyl-formamide at 75 - 80℃; | 88% |
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 | Yield |
---|---|
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% |
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 (CAS NO.148-18-5) can be used as a pesticide.
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. |
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.
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.
DFG MAK: 2 mg/m3
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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