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Sodium diethyldithiocarbamate

  • CasNo:148-18-5

Product Description

Quality products?make an important contribution to long-term revenue and profitability. Reputable factory supply Sodium diethyldithiocarbamate 148-18-5 in bulk at low price

1.What is the Sodium diethyldithiocarbamate ?

Sodium diethyldithiocarbamate is an organic molecular entity. It is an inhibitor of superoxide dismutase, having both antioxidant and oxidant effects.

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C<sub>8</sub>H<sub>15</sub>NOS<sub>4</sub>
327989-09-3

C8 H15 NOS4

bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

Conditions
Conditions Yield
With sodium nitrate; C8MoN8(3-)*3Na(1+); In water; acetone; at 25 ℃; Rate constant; Equilibrium constant; μ 0.2 mol/l;
carbon disulfide
75-15-0,12122-00-8

carbon disulfide

diethylamine
109-89-7

diethylamine

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

Conditions
Conditions Yield
With sodium hydroxide; In ethanol; water; cooling;
90%
diethylamine; With sodium hydroxide; In methanol; at 20 ℃; for 0.5h;
carbon disulfide;
82%
With sodium hydroxide; In ethanol; at 20 - 40 ℃;
73%
With sodium hydroxide; In water; at 20 ℃; for 1h; Cooling with ice;
69%
With sodium hydroxide; In methanol; other reagent;
With sodium hydroxide; In tetrahydrofuran; water; at 15 - 20 ℃; for 2h;
With sodium hydroxide; In water; Yield given;
With sodium hydroxide;
With sodium hydroxide; In ethanol; for 2h;
With sodium hydroxide; In water; at 20 ℃; for 1h; Cooling with ice;
carbon disulfide; diethylamine; In ethanol; at 5 ℃;
With sodium hydroxide; In ethanol; water;
With sodium hydroxide; pH=Ca. 6.5;
With sodium hydroxide; In ethanol; at 0 ℃;
With sodium hydroxide; In water; ethyl acetate; at 0 - 5 ℃; for 0.5h;
With sodium hydroxide; at 25 ℃; for 5h;
With sodium hydroxide; In methanol; water; at 20 ℃; for 8h; Cooling with ice;
With sodium hydroxide; In ethanol;
With sodium hydroxide; for 4h;

2.What is the CAS number for Sodium diethyldithiocarbamate ?

The CAS number of Sodium diethyldithiocarbamate is 148-18-5.

More information of Sodium diethyldithiocarbamate 148-18-5 are:

CAS?Number

148-18-5

Density

1.086 g/cm3

Melting Point

95 °C

Boiling Point

176.4 °C at 760 mmHg

Flash Point

60.5 °C

Vapor Pressure

0Pa at 20℃

HS CODE

2930909090

PSA

60.63000

LogP

1.81060

3.What are another words for Sodium diethyldithiocarbamate ?

Synonyms?for?Sodium diethyldithiocarbamate 148-18-5: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;

4.What is the molecular formula of Sodium diethyldithiocarbamate?

The chemical formula of ?Sodium diethyldithiocarbamate is?C5H10NNaS2 which containing 5 Carbon atoms,10 Hydrogen atoms,1 Nitrogen atoms,1 Sodium atoms and 2 Sulfur atoms,and the molecular weight of??Sodium diethyldithiocarbamate?is 171.263.

5.What is Sodium diethyldithiocarbamate (148-18-5) used for?

Sodium diethyldithiocarbamate is an odorless white or slightly brown or slightly pink crystalline powder. It is an organic molecular entity that is easily soluble in water and alkaline, soluble in alcohol, and rapidly decomposed in acidic aqueous solution to separate out carbon disulfide and make the solution cloudy. In an ammonia medium, it generates a precipitate or brown colloidal solution with copper ions.

InChI:InChI=1/C4H10.CH3NS2.Na/c1-3-4-2;2-1(3)4;/h3-4H2,1-2H3;(H3,2,3,4);/q;;+1/p-1

Relevant articles related to Sodium diethyldithiocarbamate:

Article

Source

Dithiocarbamates: Efficient metallo-β-lactamase inhibitors with good antibacterial activity when combined with meropenem

Wang, Ming-Ming,Chu, Wen-Chao,Yang, Yi,Yang, Qian-Qian,Qin, Shang-Shang,Zhang, En

, p. 3436 - 3440 (2018)

Synthesis and dynamic NMR studies of some new symmetrical podands of dithiocarbamates formed from Bis(N-thiazol)chloroacetamides

Shockravi, Abbas,Kamali, Mahmood,Halimehjani, Azim Ziyaei,Jafari, Reza

, p. 209 - 215 (2013)

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