Cas no 3735-92-0 (Methyl dimethyldithiocarbamate)

Methyl dimethyldithiocarbamate is a sulfur-containing organic compound primarily used as an intermediate in chemical synthesis and as a fungicide in agricultural applications. Its key advantages include high reactivity due to the dithiocarbamate functional group, which enables effective binding to metal ions and participation in coordination chemistry. The compound exhibits broad-spectrum antifungal properties, making it useful for crop protection. Its stability under controlled conditions ensures consistent performance in formulations. Additionally, the methyl group enhances its solubility in organic solvents, facilitating its incorporation into various industrial processes. Proper handling is essential due to its potential toxicity and environmental impact.
Methyl dimethyldithiocarbamate structure
3735-92-0 structure
Product Name:Methyl dimethyldithiocarbamate
CAS No:3735-92-0
MF:C4H9NS2
MW:135.250958204269
MDL:MFCD00154798
CID:307574
PubChem ID:19526
Update Time:2025-05-26

Methyl dimethyldithiocarbamate Chemical and Physical Properties

Names and Identifiers

    • Carbamodithioic acid,N,N-dimethyl-, methyl ester
    • methyl N,N-dimethylcarbamodithioate
    • CARBAMIC ACID,DIMETHYLDITHIO-,METHYL ESTER
    • Carbamodithioic acid,dimethyl-,methyl ester
    • Cystogon
    • dimethylcarbamodithioic acid methyl ester
    • Dimethyldithiocarbamic acid methyl ester
    • EINECS 223-105-5
    • Forbiat
    • Methyl dimethylcarbamodithioate
    • Methyl dimethyldithiocarbamate
    • Methyl N,N-dimethyldithiocarbamate
    • N,N,S-trimethyldithiocarbamate
    • S-methyl N,N-dimethyl dithiocarbamate
    • CARBAMIC ACID, DIMETHYLDITHIO-, METHYL ESTER
    • Carbamodithioic acid, dimethyl-, methyl ester
    • NBBZMDUHKWRYSZ-UHFFFAOYSA-N
    • N,N-dimethyl(methylsulfanyl)carbothioamide
    • WLN: SUYS1&N1&1
    • NS00030182
    • BRN 1742923
    • NSC-40176
    • DTXSID40190797
    • EN300-182825
    • AI3-03285
    • NSC40176
    • Methyl Dimethyldithiocarbam?ate
    • CHEMBL504894
    • UNII-BKH76WPU8C
    • AKOS006240950
    • CARBAMODITHIOIC ACID, N,N-DIMETHYL-, METHYL ESTER
    • SCHEMBL220119
    • AS-67643
    • Q55075175
    • BKH76WPU8C
    • Dimethyl-dithiocarbamic acid methyl ester
    • D93298
    • N,N-Dimethyl-S-methyldithiocarbamate
    • NSC 40176
    • NCI60_003772
    • 3735-92-0
    • DTXCID80113288
    • 4-04-00-00235 (Beilstein Handbook Reference)
    • MDL: MFCD00154798
    • Inchi: 1S/C4H9NS2/c1-5(2)4(6)7-3/h1-3H3
    • InChI Key: NBBZMDUHKWRYSZ-UHFFFAOYSA-N
    • SMILES: S(C)C(N(C)C)=S
    • BRN: 1742923

Computed Properties

  • Exact Mass: 135.01800
  • Monoisotopic Mass: 135.01764164g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 1
  • Complexity: 70.1
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 1.3
  • Topological Polar Surface Area: 60.6

Experimental Properties

  • PSA: 60.63000
  • LogP: 1.19590

Methyl dimethyldithiocarbamate Customs Data

  • HS CODE:2930909090
  • Customs Data:

    China Customs Code:

    2930909090

    Overview:

    2930909090. Other organic sulfur compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Methyl dimethyldithiocarbamate Pricemore >>

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Methyl dimethyldithiocarbamate Related Literature

Additional information on Methyl dimethyldithiocarbamate

Methyl dimethyldithiocarbamate (CAS No. 3735-92-0): A Comprehensive Overview

Methyl dimethyldithiocarbamate, with the chemical formula C?H?N?S? and CAS number 3735-92-0, is a significant compound in the field of organic chemistry and pharmaceutical research. This compound has garnered attention due to its versatile applications and the potential it holds in various scientific domains. Understanding its properties, synthesis, and emerging applications is crucial for researchers and professionals in the industry.

The molecular structure of methyl dimethyldithiocarbamate consists of a methyl group attached to a dithiocarbamate moiety. This unique arrangement contributes to its reactivity and makes it a valuable intermediate in the synthesis of more complex molecules. The presence of sulfur atoms in its structure also imparts specific chemical characteristics that are exploited in various biochemical processes.

In recent years, methyl dimethyldithiocarbamate has been studied extensively for its potential applications in pharmaceuticals. Its ability to act as a chelating agent has made it a candidate for developing treatments against metal toxicity. Researchers have explored its efficacy in binding heavy metals such as lead and mercury, which are known to be highly toxic to biological systems. The chelating properties of this compound have been particularly promising in preclinical studies, where it demonstrated the ability to effectively remove these hazardous metals from the body.

Beyond its role in metal chelation, methyl dimethyldithiocarbamate has shown promise in the development of novel agrochemicals. Its chemical stability and reactivity make it an excellent candidate for use in pesticides and herbicides. These compounds derived from methyl dimethyldithiocarbamate have been found to be effective in controlling pests while maintaining a lower environmental impact compared to traditional agrochemicals.

The synthesis of methyl dimethyldithiocarbamate involves several well-established chemical reactions. One common method involves the reaction of carbon disulfide with sodium methanethiolate, followed by acidification to yield the desired product. This synthetic route is favored for its simplicity and high yield, making it suitable for industrial-scale production. Additionally, advancements in green chemistry have led to the development of more environmentally friendly synthetic methods that minimize waste and reduce energy consumption.

Recent studies have also delved into the pharmacological properties of methyl dimethyldithiocarbamate. Its derivatives have been investigated for their potential anti-inflammatory and antioxidant effects. These properties make it a promising candidate for developing treatments against chronic inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease. The antioxidant activity of this compound has also been linked to its ability to scavenge free radicals, thereby protecting cells from oxidative damage.

The safety profile of methyl dimethyldithiocarbamate is another critical aspect that has been thoroughly examined. Extensive toxicological studies have been conducted to assess its acute and chronic toxicity levels. These studies have shown that when used appropriately, methyl dimethyldithiocarbamate is generally well-tolerated by living organisms. However, like any chemical compound, it is essential to handle it with care and adhere to safety protocols to prevent any potential adverse effects.

In conclusion, methyl dimethyldithiocarbamate (CAS No. 3735-92-0) is a multifaceted compound with significant applications in pharmaceuticals, agrochemicals, and material science. Its unique chemical properties make it a valuable tool for researchers working on developing new treatments and materials. As research continues to uncover more about its potential, methyl dimethyldithiocarbamate is poised to play an increasingly important role in various scientific fields.

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