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Triphenyl borate (CAS 1095-03-0)

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Alternate Names:
Triphenoxyborane; Triphenyl ester boric acid
Application:
Triphenyl borate is a useful boronic ester with chemosterilant activity against Cochliomyia hominivorax
CAS Number:
1095-03-0
Purity:
≥97%
Molecular Weight:
290.12
Molecular Formula:
C18H15BO3
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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Triphenyl borate functions as a chemical compound that acts as a flame retardant in various experimental applications. It works by inhibiting the combustion process through a mechanism that involves the release of free radicals and the interruption of the radical chain reaction. This interruption prevents the spread of fire by interfering with reactions that sustain the combustion process. At the molecular level, triphenyl borate interacts with the free radicals generated during the combustion process, leading to the formation of stable, non-reactive species that suppress the propagation of the fire. The mode of action involves its ability to disrupt the energy transfer and chemical reactions that occur during the combustion process, thereby reducing the flammability of the material to which it is applied. Triphenyl borate′s functional role in experimental involves its capacity to act as a flame retardant by interfering with the combustion process at the molecular level.


Triphenyl borate (CAS 1095-03-0) References

  1. Ozonolysis in the presence of Lewis acids: directed addition to carbonyl oxides.  |  Dussault, PH. and Raible, JM. 2000. Org Lett. 2: 3377-9. PMID: 11029215
  2. Catalytic Asymmetric Aziridination with Arylborate Catalysts Derived from VAPOL and VANOL Ligands This work was supported by the National Institutes of Health and was performed at the University of Chicago. VAPOL=2,2'-diphenyl-.  |  Antilla, JC. and Wulff, WD. 2000. Angew Chem Int Ed Engl. 39: 4518-4521. PMID: 11169656
  3. An efficient synthesis of (-)-chloramphenicol via asymmetric catalytic aziridination: a comparison of catalysts prepared from triphenylborate and various linear and vaulted biaryls.  |  Loncaric, C. and Wulff, WD. 2001. Org Lett. 3: 3675-8. PMID: 11700110
  4. Palladium-catalyzed stereospecific substitution of alpha,beta-unsaturated gamma,delta-epoxy esters by alcohols with double inversion of configuration: synthesis of 4-alkoxy-5-hydroxy-2-pentenoates.  |  Yu, XQ., et al. 2008. Angew Chem Int Ed Engl. 47: 750-4. PMID: 18069707
  5. First isolation of disubstituted cis-5,6-dihydro-1,10-phenanthrolines. Lipase-mediated resolution of cis- and trans-phenoxy alcohol isomers and assignment of absolute stereochemistry via CD and NMR spectroscopy.  |  Kohler, L., et al. 2012. Chirality. 24: 245-51. PMID: 22253063
  6. A space-sacrificed pyrolysis strategy for boron-doped carbon spheres with high supercapacitor performance.  |  Huang, S., et al. 2022. J Colloid Interface Sci. 608: 334-343. PMID: 34626979
  7. Breaking scaling relationships in alkynol semi-hydrogenation by manipulating interstitial atoms in Pd with d-electron gain.  |  Yang, Y., et al. 2022. Nat Commun. 13: 2754. PMID: 35585084
  8. Design and Preparation of Localized Heat-Resistant Coating.  |  Lin, Z., et al. 2022. Polymers (Basel). 14: PMID: 35893996

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Triphenyl borate, 10 g

sc-224323
10 g
$80.00