Substance
ID:309832
Names and Identifiers
IUPAC name
tribromoborane
IUPAC Traditional name
boron tribromide
Synonyms
Boron tribromide三溴化硼Tribromoboron
Properties
Physical Property
Flash Point
195.8 °F
91 °C
Density
2.60 g/mL at 20 °C(lit.)
Apperance
colorless
Vapor Pressure
40 mmHg ( 14 °C)
Boiling Point
~90 °C(lit.)
Vapor Density
8.6 (vs air)
Melting Point
-46 °C(lit.)
Safety Information
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
European Hazard Symbols
Highly toxic (T+)
Corrosive (C)Hazard Class
8
MSDS Link
RID/ADR
UN 2692 8/PG 1
GHS Hazard statements
H300-H314-H330
Risk Statements
14-26/28-35
GHS Signal Word
Danger
Safety Statements
9-26-28-36/37/39-45
Supplemental Hazard Statements
Reacts violently with water.
GHS Precautionary statements
P260-P264-P280-P284-P305+P351+P338-P310
German water hazard class
3
RTECS
ED7400000
UN Number
2692
Packing Group
1
Product Information
Grade
ReagentPlus®
Purity
99.9%
Empirical Formula (Hill Notation)
BBr3
Molecule Details
Application
Used to cleave aryl methyl ethers in a syntheses of a benzopyranobenzopyran from a coumarin scaffold11 and ladder-type conjugated polymers.12
Reactant for preparation of:
• Drug intermediate 6-nitro-L-DOPA1
• Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties2
• High-quality boron-doped graphene via Wurtz-type reductive coupling reaction3
• Mercapto-(+)-methamphetamine haptens for synthesis of (+)-methamphetamine conjugate vaccines with improved epitope densities4
• Micrometer-sized organic molecule-DNA hybrid structures5
• Borane complexes via electrophilic aromatic borylation reactions6
• A 5-HT2C receptor agonist7
• Biphenyl-derivatives possessing tertiary amino groups as β-secretase(BACE1) inhibitors for the treatment of Alzheimer′s disease8
• A highly near-IR region fluorescent p-extended boron aza-dipyrromethene moiety unit9
• Tetrahydroisoquinoline derivatives via intramolecular cyclization of methoxy-substituted N-phenethylimides10
Packaging
100, 250 g in Sure/Seal™
2 kg in Sure/Seal™
25 g in ampule
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
Used to cleave aryl methyl ethers in a syntheses of a benzopyranobenzopyran from a coumarin scaffold11 and ladder-type conjugated polymers.12
Reactant for preparation of:
• Drug intermediate 6-nitro-L-DOPA1
• Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties2
• High-quality boron-doped graphene via Wurtz-type reductive coupling reaction3
• Mercapto-(+)-methamphetamine haptens for synthesis of (+)-methamphetamine conjugate vaccines with improved epitope densities4
• Micrometer-sized organic molecule-DNA hybrid structures5
• Borane complexes via electrophilic aromatic borylation reactions6
• A 5-HT2C receptor agonist7
• Biphenyl-derivatives possessing tertiary amino groups as β-secretase(BACE1) inhibitors for the treatment of Alzheimer′s disease8
• A highly near-IR region fluorescent p-extended boron aza-dipyrromethene moiety unit9
• Tetrahydroisoquinoline derivatives via intramolecular cyclization of methoxy-substituted N-phenethylimides10
Packaging
100, 250 g in Sure/Seal™
2 kg in Sure/Seal™
25 g in ampule
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data