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Triflic Acid

Triflic Acid Suppliers list
Company Name: Shanghai Acmec Biochemical Technology Co., Ltd.
Tel: +undefined18621343501
Email: product@acmec-e.com
Products Intro: Cas:1493-13-6
ProductName:Triflic acid
Purity: 98% | Package: 25g, 1kg, 100g, 500g, 5g
Company Name: Auonsi (Shanghai) Biology Technology Co., Ltd.  
Tel: 400-1107768 15058188853
Email: 478133536@qq.com
Products Intro: Cas:1493-13-6
ProductName:Triflic acid
Purity: 98% | Package: 5g;25g;100g
Company Name:   
Tel:
Email: mktg@ultimachem.com
Products Intro: Cas:1493-13-6
ProductName:TRIFLIC ACID
Purity: 99% | Package: 1 kg,5 kg, 10 kg,25kg and 1 MT
Company Name:   
Tel:
Email: info@golechha.in
Products Intro: Cas:1493-13-6
ProductName:Triflic Acid
Purity: 98% | Package: 1 kg,5 kg, 10 kg,25kg and 1 MT
Company Name: Shandong longyue of chemical co., LTD  
Tel: 15318857512
Email: 1912317598@qq.com
Products Intro: Cas:1493-13-6
ProductName:triflic acid
Purity: 99.5 | Package: 1kg;25kg;1000kg

Triflic Acid manufacturers

  • triflic anhydride
  • triflic anhydride pictures
  • $80.00 / 1KG
  • 2023-08-16
  • CAS:358-23-6
  • Min. Order: 1KG
  • Purity: >99%
  • Supply Ability: 20tons
  • triflic anhydride
  • triflic anhydride pictures
  • $1.00 / 1KG
  • 2023-01-12
  • CAS:358-23-6
  • Min. Order: 0.5KG
  • Purity: >99%
  • Supply Ability: 20tons
  • triflic anhydride
  • triflic anhydride pictures
  • $60.00 / 10g
  • 2021-03-17
  • CAS:358-23-6
  • Min. Order: 10g
  • Purity: 99.8%
  • Supply Ability: 10tons

Related articles

Triflic Acid Basic information
Description Chemical Properties Preparation Uses Reactions
Product Name:Triflic Acid
Synonyms:trifluoro-methanesulfonicaci;PERFLUOROMETHANESULFONIC ACID;TRIFLUOROMETHANESULFONIC ACID;TRIMESYLATE ACID;Trifluoromethanesulfonnic acid;Trifluoromethanesulphonic acid/Triflic acid;TRIFLUOROMETHANESULFONIC ACID, LOW FLUOR;TRIFLUOROMETHANESULFONIC ACID FREE ACID
CAS:1493-13-6
MF:CHF3O3S
MW:150.08
EINECS:216-087-5
Product Categories:Organic Fluorides;organofluorine compounds;Organic AcidsVolumetric Solutions;Reference Material Potassium hydrogenphthalateTitration;Acid SolutionsChemical Synthesis;By Reference Material;Solutions for non-aqueous titrations;Synthetic Reagents;Titration;Volumetric Solutions;straight chain compounds;Pharmaceutical intermediates;1493-13-6
Mol File:1493-13-6.mol
Triflic Acid Structure
Triflic Acid Chemical Properties
Melting point -40 °C
Boiling point 162 °C (lit.)
density 1.696 g/mL at 25 °C (lit.)
vapor density 5.2 (vs air)
vapor pressure 8 mm Hg ( 25 °C)
refractive index n20/D 1.327(lit.)
RTECS PB2771000
Fp None
storage temp. Store below +30°C.
solubility Miscible in H<sub>2</sub>O
pka-14(at 25℃)
form Fuming Liquid
Specific Gravity1.696
color slightly brown
PH<1 (H2O)
Water Solubility SOLUBLE
Sensitive Hygroscopic
Merck 14,9676
BRN 1812100
Stability:Stable. Incompatible with acids, alkalis, metals.
InChIKeyITMCEJHCFYSIIV-UHFFFAOYSA-N
LogP0.3 at 25℃
CAS DataBase Reference1493-13-6(CAS DataBase Reference)
NIST Chemistry ReferenceCF3SO3H(1493-13-6)
EPA Substance Registry SystemMethanesulfonic acid, trifluoro- (1493-13-6)
Safety Information
Hazard Codes C
Risk Statements 21/22-35-10
Safety Statements 26-36/37/39-45
RIDADR UN 3265 8/PG 2
WGK Germany 2
3-10
Hazard Note Corrosive/Hygroscopic
TSCA Yes
HazardClass 8
PackingGroup II
HS Code 29049020
ToxicityLD50 orally in Rabbit: 1605 mg/kg LD50 dermal Rat > 2000 mg/kg
MSDS Information
ProviderLanguage
Trifluoromethanesulfonic acid English
SigmaAldrich English
ACROS English
ALFA English
Triflic Acid Usage And Synthesis
DescriptionTriflic acid is a one-carbon compound that is methanesulfonic acid in which the hydrogens attached to the methyl carbon have been replaced by fluorines. It is a one-carbon compound and a perfluoroalkanesulfonic acid. It is a conjugate acid of a triflate.
Uses

Triflic Acid is one of the strongest known acids, and the strongest Bronstedt acid available at industrial scale. Triflic Acid can be used as a catalyst to prepare:
Substituted tetrahydrofurans and tetrahydropyrans by cyclization of corresponding unsaturated alcohols under acidic conditions.
Nitriles from corresponding aldehydes by Schmidt reaction.
Disubstituted five-membered ring lactones by allylboration reaction between 2-alkoxycarbonyl allylboronates and aldehydes.
Used as a catalyst in the Fischer glycosylation and Friedel-Crafts acylation reactions.
Deglycosylation agent.

Tag:Triflic Acid(1493-13-6) Related Product Information
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