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Merck
CN

18127

1,1,1,3,3,3-Hexafluoro-2-propanol

for LC-MS LiChropur™

Synonym(s):

HFP, Hexafluoroisopropanol

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About This Item

Linear Formula:
(CF3)2CHOH
CAS Number:
920-66-1
Molecular Weight:
168.04
NACRES:
NA.21
UNSPSC Code:
12352104
Beilstein/REAXYS Number:
1841007
MDL number:
MFCD00011651

Key Documents

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Product Name

1,1,1,3,3,3-Hexafluoro-2-propanol, for LC-MS LiChropur™

SMILES string

OC(C(F)(F)F)C(F)(F)F

InChI key

BYEAHWXPCBROCE-UHFFFAOYSA-N

InChI

1S/C3H2F6O/c4-2(5,6)1(10)3(7,8)9/h1,10H

assay

≥99.8% (GC)

form

liquid

quality

for LC-MS LiChropur™

impurities

≤0.02% water

refractive index

n20/D 1.275 (lit.)

bp

59 °C (lit.)

mp

−4 °C (lit.)

density

1.596 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 ppm
Ca: ≤0.5 ppm
Cu: ≤0.02 ppm
Fe: ≤0.1 ppm
K: ≤2 ppm
Mg: ≤0.1 ppm
Na: ≤10 ppm

suitability

passes test for LC-MS (ESI/APCI pos. < 10 ppb)

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Application

1,1,1,3,3,3-Hexafluoro-2-propanol can be used as a:
  • Buffer additive for LC-ESI-MS to separate acidic and basic compounds.
  • Eluent additive in the UHPLC-MS/MS method to improve the chromatographic separation of basic and zwitterionic compounds.

General description

1,1,1,3,3,3-Hexafluoro-2-propanol(HFIP) is a thermally stable, highly polar, UV-transparent solvent that is misciblewith water and many polar organic solvents. It is used as a mobile phaseadditive in liquid chromatography-mass spectrometry (LC-MS) method to improveseparation and detection.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazardCorrosion
GHS08,GHS05

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Repr. 2 - Skin Corr. 1A - STOT RE 2 Oral

target_organs

Central nervous system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

No data available

flash_point_c

No data available

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN8757
BCCN8756
BCCN3247
BCCN3246
BCCN3245

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Fluoroalcohols as novel buffer components for basic buffer solutions for liquid chromatography electrospray ionization mass spectrometry: retention mechanisms
Kipper K, et al.
Journal of Chromatography A, 1218(45), 8175-8180 (2011)
Retention mechanisms of acidic and basic analytes on the Pentafluorophenyl stationary phase using fluorinated eluent additives
Lossmann K, et al.
Journal of Chromatography A, 1666, 462850-462850 (2022)
1, 1, 1, 3, 3, 3-Hexafluoro-2-propanol
Phillips AJ and Roach JJ
e-EROS Encyclopedia of Reagents for Organic Synthesis, 1-9 (2001)

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