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About This Item
Empirical Formula (Hill Notation):
BF3
CAS Number:
Molecular Weight:
67.81
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
2.38 (21 °C, vs air)
Quality Level
Assay
≥99.5%
form
gas
reaction suitability
core: boron
reagent type: Lewis acid
reagent type: catalyst
reaction type: Polymerization Reactions
bp
−100 °C (lit.)
mp
−127 °C (lit.)
SMILES string
FB(F)F
InChI
1S/BF3/c2-1(3)4
InChI key
WTEOIRVLGSZEPR-UHFFFAOYSA-N
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Monel control valve Z146978 or Monel gas regulator Z562483 is recommended.
recommended
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Inhalation - Eye Dam. 1 - Press. Gas Compr. Gas - Skin Corr. 1A
Supplementary Hazards
Storage Class Code
2A - Gases
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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G K Surya Prakash et al.
The Journal of organic chemistry, 74(22), 8659-8668 (2009-10-30)
BF(3)-monohydrate is found to be an efficient and strong acid catalyst as well as an effective protosolvating medium suitable for the hydroxyalkylation of arenes with aromatic aldehydes. This reaction has been extended to aromatic dialdehydes, such as terephthalic dicarboxaldehyde and
Gewu Lu et al.
ACS nano, 2(11), 2342-2348 (2009-02-12)
Polythiophene (Pth) films with aligned nanotubule arrays were adhered strongly on various smooth surfaces such as glass, mica, and GaAs after drying from their wet states under ambient condition. The normal and shear dry adhesion forces of the films on
G K Surya Prakash et al.
Organic letters, 13(15), 4128-4131 (2011-07-14)
The one-pot synthesis of 1,1,1-trifluoro- and 1,1-difluoro-2,2-diarylethanes from arenes and fluorinated hemiacetals in the BF(3)-H(2)O system is described. The reaction is simple, clean, and convenient, eliminating the use of organic solvents and other expensive acid systems. BF(3)-H(2)O is economic, is
Brieuc Guillerm et al.
Macromolecular rapid communications, 33(19), 1600-1612 (2012-07-05)
Polyoxazolines (POx) are increasingly being studied as polymeric building blocks due to the possibility of affording tunable properties. Additionally, as the biocompatibility and stealth behavior of POx are similar to that of poly(ethylene glycol) (PEG), it has become challenging to
Diego dos Santos Pisoni et al.
European journal of medicinal chemistry, 45(2), 526-535 (2009-12-04)
This work describes the enantioselective synthesis of a new series of terpenic chiral 9-aminotetrahydroacridine analogues. Several chiral ketones were synthesized from natural monoterpenes in an optically active form and subjected to the cyclodehydration reactions with anthranilonitrile in the presence of
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