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1,4-Butane sultone: sc-229828
1,4-Butane sultone (CAS 1633-83-6)
Alternate Names:
4-Hydroxybutane-1-sulfonic acid δ-sultone
CAS Number:
1633-83-6
Purity:
≥99%
Molecular Weight:
136.17
Molecular Formula:
C4H8O3S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Description
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SDS & Certificate of Analysis
1,4-Butane sultone facilitates the production of polymers and aids in extracting compounds due to its function as a catalyst and a solvent, respectively. The compound is also integral to the creation of chiral and heterocyclic compounds. Its chemical properties enable it to act as a potent oxidizer, capable of modifying numerous compounds, and to participate in reactions as a nucleophile, forming stable covalent bonds with a range of molecules.
References:
- Flow cytometric measurement of micronuclei induced in a permanent fish cell line as a possible screening test for the genotoxicity of industrial waste waters. | Kohlpoth, M., et al. 1999. Mutagenesis. 14: 397-402. PMID: 10390507
- On the reaction kinetics in water of 1,3-propane sultone and 1,4-butane sultone: a comparison of reaction rates and mutagenic activities of some alkylating agents. | Osterman-Golkar, S. and Wachtmeister, CA. 1976. Chem Biol Interact. 14: 195-202. PMID: 182390
- Synthesis of alkylated potato starch derivatives and their potential in the aqueous solubilization of benzo[a]pyrene. | Rosu, AM., et al. 2013. Carbohydr Polym. 93: 184-90. PMID: 23465918
- Development and evaluation of new imidazolium-based zwitterionic stationary phases for hydrophilic interaction chromatography. | Qiao, L., et al. 2013. J Chromatogr A. 1286: 137-45. PMID: 23489487
- Continuous tank reactor synthesis of highly substituted sulphobutylether beta -cyclodextrins. | Savage, T., et al. 2015. Int J Pharm. 495: 862-8. PMID: 26392244
- Synthesis of modified potato starches for aqueous solubilization of benzo[a]pyrene. | Delsarte, I., et al. 2016. Carbohydr Polym. 144: 83-8. PMID: 27083796
- Investigations of benzo[a]pyrene encapsulation and Fenton degradation by starch nanoparticles. | Delsarte, I., et al. 2018. Carbohydr Polym. 186: 344-349. PMID: 29455995
- Surface Functionalization of Magnetite Nanoparticles with Sulfonic Acid and Heteropoly Acid: Efficient Magnetically Recoverable Solid Acid Catalysts. | Hosseini, MS. and Masteri-Farahani, M. 2019. Chem Asian J. 14: 1076-1083. PMID: 30786167
- Nanostructured gamma -FeOStarch-n-Butyl SOH as New Recyclable Magnetic Catalyst for Promoting Multi-Component Reactions. | Shamsi-Sani, M., et al. 2019. J Nanosci Nanotechnol. 19: 4503-4511. PMID: 30913741
- Adsorption capacity of heavy metal ions using sultone-modified magnetic activated carbon as a bio-adsorbent. | Nejadshafiee, V. and Islami, MR. 2019. Mater Sci Eng C Mater Biol Appl. 101: 42-52. PMID: 31029336
- Sulfo-functional 3D porous cellulose/graphene oxide composites for highly efficient removal of methylene blue and tetracycline from water. | Wang, S., et al. 2019. Int J Biol Macromol. 140: 119-128. PMID: 31419562
- Enhanced Chiral Recognition Abilities of Cyclodextrin Covalent Organic Frameworks via Chiral/Achiral Functional Modification. | Wang, X., et al. 2022. ACS Appl Mater Interfaces. 14: 25928-25936. PMID: 35609238
- Unexpected synthesis of 4-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)butyl-H-sulfite as a catalyst for the synthesis of pyrazolophthalazines. | Oliaei, SS., et al. 2022. Mol Divers.. PMID: 36400897
- [Carcinogenic alkylating substances. IV. 1,3-propane sultone and 1,4-butane sultone]. | Druckrey, H., et al. 1970. Z Krebsforsch. 75: 69-84. PMID: 4325298
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,4-Butane sultone, 15 g | sc-229828D | 15 g | $35.00 | |||
1,4-Butane sultone, 25 g | sc-229828 | 25 g | $57.00 | |||
1,4-Butane sultone, 100 g | sc-229828A | 100 g | $138.00 | |||
1,4-Butane sultone, 500 g | sc-229828B | 500 g | $412.00 | |||
1,4-Butane sultone, 1 kg | sc-229828C | 1 kg | $693.00 |