American Elements

 

Boron Bromide
BBr3
Product Product Code Order or Specifications
(2N) 99% Boron Bromide B-BR-02 Contact American Elements
(3N) 99.9% Boron Bromide B-BR-03 Contact American Elements
(4N) 99.99% Boron Bromide B-BR-04 Contact American Elements
(5N) 99.999% Boron Bromide B-BR-05 Contact American Elements
Bromide IonBoron Bromide is a highly water soluble crystalline Boron source for uses compatible with Bromides and lower (acidic) pH. Most metal bromide compounds are water soluble for uses in water treatment, chemical analysis and in ultra high purity for certain crystal growth applications. Bromide in an aqueous solution can be detected by adding carbon disulfide (CS2) and chlorine. Boron Bromide is generally immediately available in most volumes. Ultra high purity and high purity compositions improve both optical quality and usefulness as scientific standards. Nanoscale (See also Nanotechnology Information and Quantum Dots) elemental powders and suspensions, as alternative high surface area forms, may be considered.American Elements produces to many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia)and follows applicable ASTM testing standards.Typical and custom packaging is available. Additional technical, research and safety (MSDS) information is available as is a Reference Calculator for converting relevant units of measurement.

Boron(B) atomic and molecular weight, atomic number and elemental symbolBoron is a Block P, Group 13, Period 2 element. The number of electrons in each of Boron's shells is 2, 3 and its electronic configuration is [He] 2s2 2p1. In its elemental form boron's CAS number is 7440-42-8. The boron atom has a radius of 79.5.pm and it's Van der Waals radius is 200.pm. Boron has an energy band gap of 1.50 to 1.56 eV, which is higher than that of either silicon or germanium. Optical characteristics include transmitting portions of the infrared. Boron is a poor conductor of electricity at room temperature but a good conductor at high temperature. Boron in its elemental form is not toxic. Amorphous Elemental Boronboron is used in pyrotechnic flares to provide a distinctive green color, and in rockets as an igniter Boric acid is also an important boron compound with major markets in textile products. Boron compounds are also extensively used in the manufacture of borosilicate Boron Bohr Modelglasses. The isotope Boron-10 is used as a control for nuclear reactors, as a shield for nuclear radiation, and in instruments used for detecting neutrons. Boron nitride has remarkable properties and can be used to make a material as hard as diamond. The nitride also behaves like an electrical insulator but conducts heat like a metal. Boron also has lubricating properties similar to graphite. Boron was first discovered by Sir Humphry Davy and J.L Gay-Lussac in 1808. The name Boron originates from a combination of carbon and the Arabic word 'buraqu meaning borax. See Boron research below.

Formula CAS No. Appearance Molecular Weight
BBr3
10294-33-4 Colorless Liquid 250.523
PRODUCT CATALOG Bromide Products Foil Submicron & Nanopowder Tolling Ultra High Purity Sputtering Target Crystal Growth Rod, Plate, Powder, etc. Home

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Recent Research & Development for Boron

  • Expression of the Arabidopsis Borate Efflux Transporter Gene, AtBOR4, in Rice Affects the Xylem Loading of Boron and Tolerance to Excess Boron. Kajikawa M, Fujibe T, Uraguchi S, Miwa K, Fujiwara T. Biosci Biotechnol Biochem. 2011 Dec 7. [Epub ahead of print] PMID: 22146734 [PubMed - as supplied by publisher]

  • Cl-BODIPYs: a BODIPY class enabling facile B-substitution. Lundrigan T, Crawford SM, Cameron TS, Thompson A. Chem Commun (Camb). 2011 Dec 6. [Epub ahead of print] PMID: 22146671 [PubMed - as supplied by publisher]

  • Size-Dependent Electrocatalytic Activity of Gold Nanoparticles on HOPG and Highly Boron-Doped Diamond Surfaces. Brülle T, Ju W, Niedermayr P, Denisenko A, Paschos O, Schneider O, Stimming U. Molecules. 2011 Dec 6;16(12):10059-77. PMID: 22146369 [PubMed - in process]

  • [Investigation of antiviral activity of adamantan boron derivaties on pandemic influenza virus models]. [No authors listed] Antibiot Khimioter. 2011;56(5-6):3-6. Russian. PMID: 22145224 [PubMed - in process]

  • Surface glycosylation of polysulfone membrane towards a novel complexing membrane for boron removal. Meng J, Yuan J, Kang Y, Zhang Y, Du Q. J Colloid Interface Sci. 2011 Nov 22. [Epub ahead of print] PMID: 22142998 [PubMed - as supplied by publisher]

  • Comparison of neutron spectrum measurement methods used for the epithermal beam of the LVR-15 research reactor. Viererbl L, Klupák V, Lahodová Z, Marek M. Appl Radiat Isot. 2011 Nov 25. [Epub ahead of print] PMID: 22138025 [PubMed - as supplied by publisher]

  • Catalytic Enantioselective 1,2-Diboration of 1,3-Dienes: Versatile Reagents for Stereoselective Allylation. Kliman LT, Mlynarski SN, Ferris GE, Morken JP. Angew Chem Int Ed Engl. 2011 Dec 1. doi: 10.1002/anie.201105716. [Epub ahead of print] PMID: 22135105 [PubMed - as supplied by publisher]

  • Graphene substrate-mediated catalytic performance enhancement of Ru nanoparticles: a first-principles study. Liu X, Yao KX, Meng C, Han Y. Dalton Trans. 2011 Dec 1. [Epub ahead of print] PMID: 22134739 [PubMed - as supplied by publisher]

  • C7H122+: A Prototype Hexacoordinate Carbonium Ion. Rasul G, Olah GA, Prakash GK. J Phys Chem A. 2011 Nov 30. [Epub ahead of print] PMID: 22129100 [PubMed - as supplied by publisher]

  • Measurements of beam current density and proton fraction of a permanent-magnet microwave ion source. Waldmann O, Ludewigt B. Rev Sci Instrum. 2011 Nov;82(11):113505. PMID: 22128974 [PubMed - in process]

  • Hydrogenation of fragment cations produced by femtosecond laser ablation of boron nitride. Kobayashi T, Matsuo Y. J Chem Phys. 2011 Nov 28;135(20):204504. PMID: 22128940 [PubMed - in process]

  • Spectroscopic and structural characterization of the CyNHC adduct of B2pin2 in solution and in the solid state. Kleeberg C, Crawford AG, Batsanov AS, Hodgkinson P, Apperley DC, Cheung MS, Lin Z, Marder TB. J Org Chem. 2011 Nov 29. [Epub ahead of print] PMID: 22126312 [PubMed - as supplied by publisher]

  • Novel retinoic Acid receptor alpha agonists for treatment of kidney disease. Zhong Y, Wu Y, Liu R, Li Z, Chen Y, Evans T, Chuang P, Das B, He JC. PLoS One. 2011;6(11):e27945. Epub 2011 Nov 18. PMID: 22125642 [PubMed - in process]

  • Structure, bonding, vibration and ideal strength of primitive-centered tetragonal boron nitride. Li Z, Gao F. Phys Chem Chem Phys. 2011 Nov 29. [Epub ahead of print] PMID: 22124285 [PubMed - as supplied by publisher]

  • Evaluation of the ions release / incorporation of the prototype S-PRG filler-containing endodontic sealer. Han L, Okiji T. Dent Mater J. 2011 Nov 25. [Epub ahead of print] PMID: 22123015 [PubMed - as supplied by publisher]

  • Kinetic Monte Carlo study on the suppression of boron transient enhanced diffusion with carbon pre-implant. Park SY, Sung KS, Won T. J Nanosci Nanotechnol. 2011 Jul;11(7):6594-8. PMID: 22121763 [PubMed - in process]

  • Synthesis of B4C nanobelts in porous SiC bodies. Jung IC, Kwon YD, Lee J, Min BK. J Nanosci Nanotechnol. 2011 Jul;11(7):6555-8. PMID: 22121755 [PubMed - in process]

  • Theoretical investigation of Ti-adsorbed graphene for hydrogen storage using the ab-initio method. Park HL, Yoo DS, Yi SC, Chung YC. J Nanosci Nanotechnol. 2011 Jul;11(7):6131-5. PMID: 22121672 [PubMed - in process]

  • Improvement of heavy dopant doped Ni-silicide using ytterbium interlayer for nano-scale MOSFETS with an ultra shallow junction. Shin HS, Oh SK, Kang MH, Li SG, Lee GW, Lee HD. J Nanosci Nanotechnol. 2011 Jul;11(7):5628-32. PMID: 22121582 [PubMed - in process]

  • A novel fluorescent probe for Au(iii)/Au(i) ions based on an intramolecular hydroamination of a Bodipy derivative and its application to bioimaging. Wang JB, Wu QQ, Min YZ, Liu YZ, Song QH. Chem Commun (Camb). 2011 Nov 28. [Epub ahead of print] PMID: 22121504 [PubMed - as supplied by publisher]

 

Recent Research & Development for Bromides

  • Synthesis of Enol Lactones via Cu(I)-Catalyzed Intramolecular O-Vinylation of Carboxylic Acids. Sun C, Fang Y, Li S, Zhang Y, Zhao Q, Zhu S, Li C. Org Lett. 2010 Jan 5. [Epub ahead of print] PMID: 19689116 [PubMed - as supplied by publisher]

  • Formation of ArF from LPdAr(F): Catalytic Conversion of Aryl Triflates to Aryl Fluorides. Watson DA, Su M, Teverovskiy G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald SL. Science. 2009 Aug 13. [Epub ahead of print] PMID: 19679769 [PubMed - as supplied by publisher]

  • (2-Pyridyl)acetone-Promoted Cu-Catalyzed O-Arylation of Phenols with Aryl Iodides, Bromides, and Chlorides. Zhang Q, Wang D, Wang X, Ding K. J Org Chem. 2009 Aug 12. [Epub ahead of print] PMID: 19673481 [PubMed - as supplied by publisher]

  • Ni-Catalyzed Sonogashira Coupling of Nonactivated Alkyl Halides: Orthogonal Functionalization of Alkyl Iodides, Bromides, and Chlorides. Vechorkin O, Barmaz D, Proust V, Hu X. J Am Chem Soc. 2009 Aug 11. [Epub ahead of print] PMID: 19670863 [PubMed - as supplied by publisher]

  • Zn-mediated electrochemical allylation of aldehydes in aqueous ammonia. Huang JM, Dong Y. Chem Commun (Camb). 2009 Jul 14;(26):3943-5. Epub 2009 May 28. PMID: 19662260 [PubMed - in process]

  • Practical Catalytic Asymmetric Synthesis of Diaryl-, Aryl Heteroaryl-, and Diheteroarylmethanols. Salvi L, Kim JG, Walsh PJ. J Am Chem Soc. 2009 Aug 4. [Epub ahead of print] PMID: 19653691 [PubMed - as supplied by publisher]

  • Direct Palladium-Catalyzed Arylations of Aryl Bromides with 2/9-Substituted Pyrimido[5,4-b]indolizines. Jiang M, Li T, Meng L, Yang C, Xie Y, Ding J. J Comb Chem. 2009 Jul 31. [Epub ahead of print] PMID: 19645499 [PubMed - as supplied by publisher]

  • Versatile chemoselectivity in Ni-catalyzed multiple bond carbonylations and cyclocarbonylations in CO(2)-expanded liquids. del Moral D, Banet Osuna AM, Córdoba A, Moretó JM, Veciana J, Ricart S, Ventosa N. Chem Commun (Camb). 2009 Aug 21;(31):4723-5. Epub 2009 Jun 29. PMID: 19641822 [PubMed - in process]

  • Highly Selective Biaryl Cross-Coupling Reactions between Aryl Halides and Aryl Grignard Reagents: A New Catalyst Combination of N-Heterocyclic Carbenes and Iron, Cobalt, and Nickel Fluorides. Hatakeyama T, Hashimoto S, Ishizuka K, Nakamura M. J Am Chem Soc. 2009 Jul 29. [Epub ahead of print] PMID: 19639999 [PubMed - as supplied by publisher]

  • Hexacationic Dendriphos Ligands in the Pd-Catalyzed Suzuki-Miyaura Cross-Coupling Reaction: Scope and Mechanistic Studies. Snelders DJ, van Koten G, Klein Gebbink RJ. J Am Chem Soc. 2009 Jul 29. [Epub ahead of print] PMID: 19639941 [PubMed - as supplied by publisher]

  • Can One Predict Changes from S(N)1 to S(N)2 Mechanisms? Phan TB, Nolte C, Kobayashi S, Ofial AR, Mayr H. J Am Chem Soc. 2009 Jul 27. [Epub ahead of print] PMID: 19634906 [PubMed - as supplied by publisher]

  • A General Copper-Catalyzed Coupling of Azoles with Vinyl Bromides. Liao Q, Wang Y, Zhang L, Xi C. J Org Chem. 2009 Jul 15. [Epub ahead of print] PMID: 19603753 [PubMed - as supplied by publisher]

  • Kinetics of Bromine-Magnesium Exchange Reactions in Heteroaryl Bromides. Shi L, Chu Y, Knochel P, Mayr H. Org Lett. 2009 Jul 14. [Epub ahead of print] PMID: 19601592 [PubMed - as supplied by publisher]

  • C5-Modified nucleosides exhibiting anticancer activity. Lee YS, Park SM, Kim HM, Park SK, Lee K, Lee CW, Kim BH. Bioorg Med Chem Lett. 2009 Aug 15;19(16):4688-91. Epub 2009 Jun 21. PMID: 19596579 [PubMed - in process]

  • Palladium-Catalyzed Coupling of Ammonia with Aryl Chlorides, Bromides, Iodides, and Sulfonates: A General Method for the Preparation of Primary Arylamines. Vo GD, Hartwig JF. J Am Chem Soc. 2009 Jul 10. [Epub ahead of print] PMID: 19591470 [PubMed - as supplied by publisher]

  • New One-Pot Synthesis of (E)-beta-Aryl Vinyl Halides from Styrenes. Pawluc´ P, Hreczycho G, Szudkowska J, Kubicki M, Marciniec B. Org Lett. 2009 Jul 2. [Epub ahead of print] PMID: 19572730 [PubMed - as supplied by publisher]

  • The Scope and Limitation of Nickel-Catalyzed Aminocarbonylation of Aryl Bromides from Formamide Derivatives. Jo Y, Ju J, Choe J, Song KH, Lee S. J Org Chem. 2009 Jul 2. [Epub ahead of print] PMID: 19572571 [PubMed - as supplied by publisher]

  • Electroencephalographic and behavioral convulsant effects of hydrobromide and hydrochloride salts of bupropion in conscious rodents. Henshall DC, Dürmüller N, White HS, Williams R, Moser P, Dunleavy M, Silverstone PH. Neuropsychiatr Dis Treat. 2009;5:189-206. Epub 2009 Apr 8. PMID: 19557114 [PubMed - in process]

  • A facile route to C2-substituted imidazolium ionic liquids. Ennis E, Handy ST. Molecules. 2009 Jun 19;14(6):2235-45. PMID: 19553895 [PubMed - in process]

  • Synthesis of 1,3-amino alcohol derivatives via a silicon-mediated ring-opening of substituted piperidines. McCall WS, Comins DL. Org Lett. 2009 Jul 2;11(13):2940-2. PMID: 19552467 [PubMed - indexed for MEDLINE]

     

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