288462
Phosphorus tribromide
≥99.99% trace metals basis
Synonym(s):
Phosphorus(III) bromide
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
vapor pressure
0.27 psi ( 54 °C)
Quality Level
Assay
≥99.99% trace metals basis
form
liquid
refractive index
n20/D 1.697 (lit.)
bp
175 °C (lit.)
mp
−41.5 °C (lit.)
density
2.88 g/mL at 20 °C (lit.)
SMILES string
BrP(Br)Br
InChI
1S/Br3P/c1-4(2)3
InChI key
IPNPIHIZVLFAFP-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
Phosphorus tribromide (PBr3) is a phosphorus halide that can be used as a reactive phosphorylating agent for the formation of multifunctional thiophenes.
Application
PBr3 can be used as an acceptor molecule in the formation of donor-acceptor complexes. It can also be used in the phosphorylation of arylphospholes which can further be utilized in the synthesis of phosphonic amides.
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Supplementary Hazards
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Site-selective phosphorylation of arylphospholes through reaction with phosphorus tribromide
Journal of Organometallic Chemistry, 643(11), 32-38 (2002)
Donor-acceptor complexes between organoamines and phosphorus tribromide
Zeitschrift fur Naturforschung B, 56(11), 1163-1171 (2001)
Phosphorylation of 2-(3-methyl-1, 3-diazabuten-1-yl)-3-ethoxycarbonylthiophenes with phosphorus (III) halides
Heteroatom Chem., 12(7), 641-651 (2001)
Nature chemistry, 7(7), 562-568 (2015-06-24)
'Roaming' is a new and unusual class of reaction mechanism that has recently been discovered in unimolecular dissociation reactions of isolated molecules in the gas phase. It is characterized by frustrated bond cleavage, after which the two incipient fragments 'roam'
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service