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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 422-05-9 Chemical Structure| 422-05-9
Chemical Structure| 422-05-9
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Product Details of 2,2,3,3,3-Pentafluoro-1-propanol

CAS No. :422-05-9
Formula : C3H3F5O
M.W : 150.05
SMILES Code : OCC(F)(F)C(F)(F)F
MDL No. :MFCD00004673
InChI Key :PSQZJKGXDGNDFP-UHFFFAOYSA-N
Pubchem ID :9872

Safety of 2,2,3,3,3-Pentafluoro-1-propanol

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H315-H319-H332-H335
Precautionary Statements:P240-P243-P261-P264-P271-P210-P233-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P380-P362-P374-P403+P235-P404-P501
Class:3
UN#:1993
Packing Group:

Application In Synthesis of 2,2,3,3,3-Pentafluoro-1-propanol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 422-05-9 ]

[ 422-05-9 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 422-64-0 ]
  • [ 422-05-9 ]
YieldReaction ConditionsOperation in experiment
99% With hydrogen;Rh/C; In water; at 20 - 90℃; under 7500.75 Torr; for 18h; 2.15 g of 5 wtpercent Rh/C catalyst was introduced together with 32.8 g of water and 39.8 g of perfluoropropionic acid at room temperature into an autoclave reactor. The reactor was then purged with helium. H2 was bubbled into the solution via a dipping tube at a flow-rate of 8 liter / h. The pressure was set to 10 bar and the reactor temperature was increased to 90°C. After 18 hours, the autoclave was cooled down to room temperature and vented. The collected liquid phase was filtered and then introduced into a decantation funnel. The lower phase containing the pentafluoropropanol was separated and distilled in the presence of anhydrous H2SO4 (30 wtpercent) to give pure pentafluoropropanol containing 50 ppm of water (quantitative yield measured by gas chromatography (GC)). The yield in pentafluoropropanol was 99 percent.
  • 2
  • [ 422-05-9 ]
  • [ 356-42-3 ]
  • [ 3471-31-6 ]
  • [5-Methoxy-1-(2,2,3,3,3-pentafluoro-propionyl)-1H-indol-3-yl]-acetic acid 2,2,3,3,3-pentafluoro-propyl ester [ No CAS ]
  • 3
  • [ 422-05-9 ]
  • [ 3471-31-6 ]
  • [ 407-25-0 ]
  • [5-Methoxy-1-(2,2,2-trifluoro-acetyl)-1H-indol-3-yl]-acetic acid 2,2,3,3,3-pentafluoro-propyl ester [ No CAS ]
  • 4
  • [ 422-05-9 ]
  • [ 1835-65-0 ]
  • 3,4,5,6-Tetrakis-(2,2,3,3,3-pentafluoro-propoxy)-phthalonitrile [ No CAS ]
  • 5
  • [ 78385-26-9 ]
  • [ 422-05-9 ]
  • 3-[(2,2,3,3,3-pentafluoropropoxy)methyl]-3-methyloxetane [ No CAS ]
YieldReaction ConditionsOperation in experiment
57% With tetrabutylammomium bromide; potassium hydroxide; In water; at 95℃; for 24h;Inert atmosphere; 3-(Bromomethyl)-3-methyloxetane (5.07g, 30.76mmol), pentafluoropropan-1-ol (4.73g, 31.49mmol), tetrabutylammonium bromide (246.3mg, 0.764mmol) and water (4.5mL) were added to a 100mL round-bottom flask with stir bar, flask flushed with argon and heated to 95C. Potassium hydroxide (4.36g, 40% solution in water) was added over 10min to the stirring reaction at 95C. Reaction was left overnight under argon. Mixture was then allowed to cool to room temperature and dichloromethane (12mL) was added and layers separated. The aqueous layer was extracted with dichloromethane (20mL). Combined organic layers were dried over anhydrous magnesium sulfate and the solvent gently removed by rotary evaporation. The remaining oil was purified by vacuum distillation, collection fractions at 20C to yield 1.05g (57% yield). 1H NMR (400MHz, CDCl3): delta 4.49 (d, J=6Hz, 2H), 4.37 (d, J=6Hz, 2H), 3.96 (tq, J=12, 1.2Hz, 2H), 3.69 (s, 2H) 1.32 (s, 3H). 13C NMR (100MHz, CDCl3): 79.83, 78.32, 68.24 (t, J=26.8Hz), 40.15, 21.11. Carbons containing F?s were not visible with the used acquisition scans. 19F NMR (376MHz, CDCl3): -84.01 (s, 3F), -123.59 (t, J=12.4Hz, 2F).
  • 6
  • [ 2207-32-1 ]
  • [ 422-05-9 ]
  • 5-(2,2,3,3,3-pentafluoropropoxy)benzo[c][1,2,5]thiadiazole [ No CAS ]
 

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