|Related Categories||Boron, Catalysis and Inorganic Chemistry, Chemical Synthesis, Ionic Polymerization Initiators, Lewis Acids,|
|vapor density||2.38 (21 °C, vs air)|
170 g in steel cylinder
Monel control valve Z146978 or Monel gas regulator Z562483 is recommended.
Certificate of Analysis
|Precautionary statements||P260-P280-P284-P305 + P351 + P338-P310-P410 + P403|
|Supplemental Hazard Statements||Reacts violently with water.|
|Personal Protective Equipment||Faceshields, Gloves, Goggles, half-mask respirator (US), multi-purpose combination respirator cartridge (US)|
|Hazard Codes (Europe)||T+,C|
|Risk Statements (Europe)||14-26-35|
|Safety Statements (Europe)||9-26-28-36/37/39-45|
|RIDADR||UN 1008 8(2.3)|
Fluoroanalogs of DDT: superacidic BF3-H2O catalyzed facile synthesis of 1,1,1-trifluoro-2,2-diarylethanes and 1,1-difluoro-2,2-diarylethanes. Prakash GK, Paknia F, Mathew T, et al. Org. Lett. 13(15), 4128-31, (2011)
BF3-H2O catalyzed hydroxyalkylation of aromatics with aromatic aldehydes and dicarboxaldehydes: efficient synthesis of triarylmethanes, diarylmethylbenzaldehydes, and anthracene derivatives. Prakash GK, Panja C, Shakhmin A, et al. J. Org. Chem. 74(22), 8659-68, (2009)
Nucleophilic addition of potassium alkynyltrifluoroborates to D-glucal mediated by BF3 x OEt2: highly stereoselective synthesis of alpha-C-glycosides. Vieira AS, Fiorante PF, Hough TL, et al. Org. Lett. 10(22), 5215-8, (2008)
Ultra trace determination of fluorobenzoic acids in tap and reservoir water using solid-phase extraction and gas chromatography-mass spectrometry. Müller K and Seubert A J. Chromatogr. A 1260, 9-15, (2012)
Isotope effects associated with the preparation and methylation of fatty acids by boron trifluoride in methanol for compound-specific stable hydrogen isotope analysis via gas chromatography/thermal conversion/isotope ratio mass spectrometry. Chivall D, Berstan R, Bull ID, et al. Rapid Commun. Mass Spectrom. 26(10), 1232-40, (2012)
Synthesis and antioxidant activity of a novel class of 4,6-O-protected O-glycosides and their utility in disaccharide synthesis. Rajaganesh R, Jayakumar J, Sivaraj C, et al. Carbohydr. Res. 345(12), 1649-57, (2010)
Synthesis and AChE inhibitory activity of new chiral tetrahydroacridine analogues from terpenic cyclanones. dos Santos Pisoni D, Sobieski da Costa J, Gamba D, et al. Eur. J. Med. Chem. 45(2), 526-35, (2010)
Fieser 1,68 / Fieser 3,32 / Fieser 5,51 / Fieser 7,31 / Fieser 10,50 / Fieser 11,71
Corp MSDS 1 (1), 482:D / RegBook 1 (3), 3307:A / Vapor Phase 3, 1687:B
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