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4092-82-4

Carbamodithioic acid, bis(1-methylethyl)-, sodium salt, also known as sodium diisopropyldithiocarbamate, is a chemical compound with the formula C7H13NS2Na. It is a yellowish-white crystalline solid that is soluble in water and ethanol. Carbamodithioic acid, bis(1-methylethyl)-, sodium salt is primarily used as a fungicide, specifically in the protection of crops against various fungal diseases. It works by inhibiting the growth and development of fungi, thereby helping to maintain crop health and yield. Sodium diisopropyldithiocarbamate is also used in the rubber industry as an accelerator, promoting the vulcanization process. Due to its potential health and environmental risks, it is important to handle this chemical with care and follow proper safety guidelines.

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  • 4092-82-4 Structure

  • Basic information

    1. Product Name: Carbamodithioic acid, bis(1-methylethyl)-, sodium salt
    2. Synonyms: Carbamodithioic acid, bis(1-methylethyl)-, sodium salt
    3. CAS NO:4092-82-4
    4. Molecular Formula: C7H14NS2*Na
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4092-82-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 207.1°Cat760mmHg
    3. Flash Point: 79.1°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 0.229mmHg at 25°C
    7. Refractive Index: 1.535
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Carbamodithioic acid, bis(1-methylethyl)-, sodium salt(CAS DataBase Reference)
    11. NIST Chemistry Reference: Carbamodithioic acid, bis(1-methylethyl)-, sodium salt(4092-82-4)
    12. EPA Substance Registry System: Carbamodithioic acid, bis(1-methylethyl)-, sodium salt(4092-82-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4092-82-4(Hazardous Substances Data)

4092-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4092-82-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4092-82:
(6*4)+(5*0)+(4*9)+(3*2)+(2*8)+(1*2)=84
84 % 10 = 4
So 4092-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NS2/c1-5(2)8(6(3)4)7(9)10/h5-6H,1-4H3,(H,9,10)

4092-82-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,di(propan-2-yl)carbamodithioic acid

1.2 Other means of identification

Product number -
Other names N,n-diisopropyldithiocarbamic acid sodium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4092-82-4 SDS

4092-82-4Relevant articles and documents

Reduction Potentials of Thiuram Disulfide/Dithiocarbamate Couples in Acetone/Water

Nichols, Peter J.,Grant, Michael W.

, p. 2455 - 2463 (2007/10/02)

Reduction potentials relative to the saturated calomel electrode, Eo, of a series of thiuram disulfide/dithiocarbamate couples have been measured in 30percent v/v water in acetone and at μ 0.2 mol l-1 (NaNO3) by a combination of potentiometric measurements and equilibrium constant determinations for thiolate/disulfide interchange reactions.Eo values lie in the range -250 to -340 mV which place dithiocarbamates as intermediate between thiophenolate (Eo -540 mV) and ethylxanthate (Eo -206 mV) in reducing properties.The significant effect on Eo of varying the substituents on the nitrogen in the dithiocarbamates correlates with the substituent effects on the acid dissociation constants of the parent dithiocarbamic acid and with trends in the half-wave potentials for metal-based oxidation and reduction of transition metal dithiocarbamate complexes.

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