Date published: 2026-4-27

1-800-457-3801

SCBT Portrait Logo
Seach Input

Sulfosate (CAS 81591-81-3)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Avans 330; Glyphosate Mono(trimethylsulfonium) Salt
CAS Number:
81591-81-3
Molecular Weight:
245.23
Molecular Formula:
C6H16NO5PS
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.

QUICK LINKS

Sulfosate is a widely used compound in research applications, particularly in the fields of agriculture, plant science, and environmental science. It is primarily known for its role as a broad-spectrum herbicide, which means it is used to control a wide range of plant species. This makes it useful for researchers studying plant growth, plant competition, and the impact of plant species on ecological systems. In agriculture-based research, sulfosate is often utilized in studies investigating crop yield and the effectiveness of weed control strategies. It provides an efficient means to control unwanted vegetation, allowing researchers to better understand how various plant species interact and compete for resources. Additionally, the impact of sulfosate on soil health and microbial communities is a topic of ongoing research, providing valuable insights into the complex interactions between plants, soils, and microorganisms. In environmental science, sulfosate is used in research to understand its fate and transport in the environment, such as its breakdown products, its persistence in soil and water, and its impact on non-target species. This information is for risk assessments and the development of guidelines for its safe and sustainable use. Furthermore, the molecular structure of sulfosate, with its phosphonic and sulfonic acid functional groups, makes it an interesting subject for chemical and biochemical research.


Sulfosate (CAS 81591-81-3) References

  1. Sulfonate-sulfur metabolism and its regulation in Escherichia coli.  |  van der Ploeg, JR., et al. 2001. Arch Microbiol. 176: 1-8. PMID: 11479697
  2. Bone tissue response to titanium implant surfaces modified with carboxylate and sulfonate groups.  |  Kerner, S., et al. 2010. J Mater Sci Mater Med. 21: 707-15. PMID: 19902334
  3. Dissociation of dicarboxylate and disulfonate dianions.  |  Ard, S., et al. 2010. J Chem Phys. 132: 094301. PMID: 20210392
  4. Profiling sulfonate ester stability: identification of complementary protecting groups for sulfonates.  |  Miller, SC. 2010. J Org Chem. 75: 4632-5. PMID: 20515067
  5. Allosteric effects of sulfonate anions on the rates of iron release from serum transferrin.  |  Sharma, R. and Harris, WR. 2011. J Inorg Biochem. 105: 1148-55. PMID: 21708099
  6. A trifluoroacetic acid-labile sulfonate protecting group and its use in the synthesis of a near-IR fluorophore.  |  Pauff, SM. and Miller, SC. 2013. J Org Chem. 78: 711-6. PMID: 23167708
  7. Testing for departures from additivity in mixtures of perfluoroalkyl acids (PFAAs).  |  Carr, CK., et al. 2013. Toxicology. 306: 169-75. PMID: 23470359
  8. Nickel-catalyzed decarboxylative cross-coupling of perfluorobenzoates with aryl halides and sulfonates.  |  Sardzinski, LW., et al. 2015. Org Lett. 17: 1256-9. PMID: 25700128
  9. Boronate, trifluoroborate, sulfone, sulfinate and sulfonate congeners of oseltamivir carboxylic acid: Synthesis and anti-influenza activity.  |  Hong, BT., et al. 2019. Eur J Med Chem. 163: 710-721. PMID: 30576902
  10. Glycyl Radical Enzymes and Sulfonate Metabolism in the Microbiome.  |  Wei, Y. and Zhang, Y. 2021. Annu Rev Biochem. 90: 817-846. PMID: 33823652
  11. Separation and characterization of sulfonates in dissolved organic matter from industrial wastewater by solid phase extraction and high-resolution mass spectrometry.  |  Deng, W., et al. 2022. Anal Bioanal Chem. 414: 4697-4706. PMID: 35551427
  12. Anti-HSV Activity of Metallic Nanoparticles Functionalized with Sulfonates vs. Polyphenols.  |  Tomaszewska, E., et al. 2022. Int J Mol Sci. 23: PMID: 36361890
  13. Hydrogel Based on Polyhydroxyalkanoate Sulfonate: Control of the Swelling Rate by the Ionic Group Content.  |  Brelle, L., et al. 2023. Biomacromolecules. 24: 1871-1880. PMID: 36967640
  14. Microbial desulfonation.  |  Cook, AM., et al. 1998. FEMS Microbiol Rev. 22: 399-419. PMID: 9990724

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Sulfosate, 50 mg

sc-474007
50 mg
$388.00