Date published: 2026-4-25

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Ferbam (CAS 14484-64-1)

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Alternate Names:
Iron(III) dimethyldithiocarbamate
CAS Number:
14484-64-1
Molecular Weight:
416.49
Molecular Formula:
C9H18FeN3S6
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ferbam is a chemical compound that functions as a broad-spectrum fungicide. It acts by inhibiting the enzyme activity involved in the biosynthesis of methionine, an amino acid in fungi. This disruption of methionine biosynthesis ultimately leads to the inhibition of fungal growth and reproduction. Ferbam′s mechanism of action involves binding to the sulfhydryl groups of enzymes, disrupting their function and leading to the inhibition of fungal cell division and growth. Ferbam′s mechanism of action at the molecular level involves interfering with the normal metabolic processes of fungi, ultimately leading to their demise. Ferbam′s role in experimental applications involves the effects of inhibiting specific enzyme pathways in fungi, providing insights into potential targets for fungicidal compounds.


Ferbam (CAS 14484-64-1) References

  1. Direct spectrophotometric determination of ferbam (Iron(III) dimethyldithiocarbamate) in commercial sample and wheat grains using 4,7-diphenyl-1,10-phenanthroline.  |  Malik, AK. 2000. J Agric Food Chem. 48: 5808-11. PMID: 11141253
  2. Metabolism and disposition of ferbam in the rat.  |  Hodgson, JR., et al. 1975. Toxicol Appl Pharmacol. 33: 505-13. PMID: 1237951
  3. Evaluation of the aneugenic potential of the fungicide Ferbam in mice.  |  Shanthi, R. and Krishnamoorthy, M. 2002. Teratog Carcinog Mutagen. 22: 451-9. PMID: 12395406
  4. Capillary electrophoretic-ultraviolet method for the separation and estimation of zineb, maneb, and ferbam in food samples.  |  Aulakh, JS., et al. 2007. J AOAC Int. 90: 834-7. PMID: 17580637
  5. Spectrophotometric determination of ziram, ferbam and zineb with diphenylcarbazone.  |  Malik, AK. and Rao, AL. 1991. Talanta. 38: 941-4. PMID: 18965241
  6. Spectrophotometric determination of iron(III) dimethyldithiocarbamate (ferbam).  |  Malik, AK. and Rao, AL. 1997. Talanta. 44: 177-83. PMID: 18966732
  7. Effect of DNOC, Ferbam and Imidan exposure on mouse sperm morphology.  |  Quinto, I., et al. 1989. Mutat Res. 224: 405-8. PMID: 2555709
  8. [Nursing care planning of patients during the surgical period: teaching of nursing students. I].  |  Pfeiffer Castellanos, BE., et al. 1978. Rev Esc Enferm USP. 12: 150-5. PMID: 257679
  9. Alteration of the Nonsystemic Behavior of the Pesticide Ferbam on Tea Leaves by Engineered Gold Nanoparticles.  |  Hou, R., et al. 2016. Environ Sci Technol. 50: 6216-23. PMID: 27254832
  10. Au@Ag-TGANPs based SERS for facile screening of thiabendazole and ferbam in liquid milk.  |  Hussain, A., et al. 2021. Spectrochim Acta A Mol Biomol Spectrosc. 245: 118908. PMID: 32949944
  11. Development of cellulose Nanofiber-based substrates for rapid detection of ferbam in kale by Surface-enhanced Raman spectroscopy.  |  Sun, L., et al. 2021. Food Chem. 347: 129023. PMID: 33484959
  12. Synthesis of bimetallic core-shelled nanoparticles modified by 2-mercaptoethanol as SERS substrates for detecting ferbam and thiabendazole in apple puree.  |  Hussain, N., et al. 2021. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 38: 1386-1399. PMID: 34157962
  13. Sensitive detection of ferbam by coupling solid phase microextraction with surface enhanced Raman spectroscopy based on Au nano-glass capillary.  |  Wang, C., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 272: 120960. PMID: 35158138
  14. Oral toxicity of ferric dimethyl-dithiocarbamate (ferbam) and tetramethylthiuram disulfide (thiram) in rodents.  |  Lee, CC., et al. 1978. J Toxicol Environ Health. 4: 93-106. PMID: 633415

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ferbam, 250 mg

sc-228118
250 mg
$50.00