Skip to Content
Merck
CN

257478

2,2,3,3,3-Pentafluoro-1-propanol

97%

Synonym(s):

PFPOH

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CF3CF2CH2OH
CAS Number:
Molecular Weight:
150.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-012-7
Beilstein/REAXYS Number:
1743133
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2,2,3,3,3-Pentafluoro-1-propanol, 97%

InChI key

PSQZJKGXDGNDFP-UHFFFAOYSA-N

InChI

1S/C3H3F5O/c4-2(5,1-9)3(6,7)8/h9H,1H2

SMILES string

OCC(F)(F)C(F)(F)F

assay

97%

form

liquid

refractive index

n20/D 1.288 (lit.)

bp

80 °C/748 mmHg (lit.)

density

1.505 g/mL at 25 °C (lit.)

functional group

fluoro
hydroxyl

Quality Level

Looking for similar products? Visit Product Comparison Guide

Application

2,2,3,3,3-Pentafluoro-1-propanol has been used:
  • as derivatization reagent in detection of unlabeled and 15N2 -labeled L-tryptophan, L-kynurenine, serotonin and quinolinic acid in human and rat plasma by GC-MS
  • as derivatization reagent in simultaneous analysis of cocaine, cocaethylene and their possible metabolic and pyrolytic products in blood, urine and muscle by GC-MS
  • preparation of trifluoromethyl ynamines which, in turn, converted aldehydes to α-trifluoromethyl-α,β-unsaturated amides
  • to generate fluorinated α-keto ethers with alkenes and has wide applications in the expanding fluorous research area

General description

2,2,3,3,3-Pentafluoro-1-propanol is an alternative cleaning agent for chlorofluorocarbon.

pictograms

Health hazardExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - STOT RE 2 Inhalation

target_organs

Liver

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ishihara, T.; et al.
Tetrahedron, 62, 3783-3783 (2006)
Patrick S Cardona et al.
Forensic science international, 157(1), 46-56 (2006-01-24)
A method was developed for simultaneously analyzing cocaine (COC), benzoylecgonine (BZE), norbenzoylecgonine (BNE), norcocaine (NCOC), ecgonine (ECG), ecgonine methyl ester (EME), m-hydroxybenzoylecgonine (HBZE), anhydroecgonine methyl ester (AEME), cocaethylene (CE), norcocaethylene (NCE), and ecgonine ethyl ester (EEE) in blood, urine, and
Mitsue Sano et al.
Journal of mass spectrometry : JMS, 49(2), 128-135 (2014-03-29)
A method for the detection of unlabeled and (15)N2 -labeled L-tryptophan (L-Trp), L-kynurenine (L-Kyn), serotonin (5-HT) and quinolinic acid (QA) in human and rat plasma by GC/MS is described. Labeled and unlabeled versions of these four products were analyzed as
M Usami et al.
Kokuritsu Iyakuhin Shokuhin Eisei Kenkyujo hokoku = Bulletin of National Institute of Health Sciences, (118)(118), 45-49 (2001-09-06)
Teratogenicity of 2,2,3,3,3-pentafluoro-1-propanol (5FP), an alternative cleaning agent for chlorofluorocarbon, was examined in rats. 5FP was diluted with sesame oil and given to pregnant rats (Crj: Wistar) by gavage once a day from day 7 to 17 of pregnancy at
Sudha Manandhar et al.
The Journal of organic chemistry, 67(18), 6415-6420 (2002-08-31)
Interactions of various fluorinated and nonfluorinated alcohols with trans-stilbene in the presence of electrophilic reagents were studied. Under neat conditions, reactions of trans-stilbene (1) with fluorinated alcohols, R(f)OH (R(f) = CF3CH2-, CFH2CH2-, CF3CF2CH2-, CF2H(CF2)3CH2-, (CF3)2CH-, (CF3)3C- (2a-f) in the presence

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