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Key Documents

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76735

Supelco

O-(2,3,4,5,6-Pentafluorobenzyl)hydroxylamine hydrochloride

for GC derivatization, LiChropur™, ≥99.0% (AT)

Sinónimos:

PFBHA·HCl

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About This Item

Fórmula lineal:
C6F5CH2ONH2·HCl
Número de CAS:
57981-02-9
Peso molecular:
249.57
Beilstein/REAXYS Number:
4031190
EC Number:
261-057-7
MDL number:
MFCD00012953
UNSPSC Code:
12000000
PubChem Substance ID:
329767306
NACRES:
NA.22

grade

for GC derivatization

Quality Level

100

assay

≥99.0% (AT)

form

solid

quality

LiChropur™

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

technique(s)

gas chromatography (GC): suitable

mp

212-218 °C
227 °C (subl.) (lit.)

solubility

H2O: 5%, clear

SMILES string

Cl.NOCc1c(F)c(F)c(F)c(F)c1F

InChI

1S/C7H4F5NO.ClH/c8-3-2(1-14-13)4(9)6(11)7(12)5(3)10;/h1,13H2;1H

InChI key

HVMVKNXIMUCYJA-UHFFFAOYSA-N

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General description

O-(2,3,4,5,6-Pentafluorobenzyl)hydroxylamine hydrochloride (PFBHA.HCl) is a derivatizing agent.

Application

PFBHA.HCl has been used for derivatization of metabolites with carbonyl groups followed by analysis via GC-MS. It has also been used in aldehyde derivatization followed by aldehydic hydrolysis using GC/MS.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Sensitive derivatizing agent for electron capture gas chromatographic analysis of carbonyl-containing compounds: keto steroids and carbohydrates

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCM3788
BCCH0583
BCCH6337
BCCG5577
BCCF8143

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Degradation of fluoranthene by Pasteurella sp. IFA and Mycobacterium sp. PYR-1:isolation and identification of metabolites.
Sepic E, Bricelj M, Leskovsek H.
Journal of Applied Microbiology, 85(4), 746-754 null
Plasmalogen degradation by oxidative stress: production and disappearance of specific fatty aldehydes and fatty alpha-hydroxyaldehydes.
Stadelmann-Ingrand S
Free Radical Biology & Medicine, 31(10), 1263-1271 (2001)
Y W Lin et al.
Applied occupational and environmental hygiene, 15(11), 855-862 (2000-11-04)
Ketones are the major positive interferences for an aldehyde dynamic air sampler that consists of 200-mg 20 percent (w/w) O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine hydrochloride (PFBHA) on Tenax TA contained in a Pyrex tube 7-mm OD, 5-mm ID, and 70-mm in length, that utilizes
S Friedfeld et al.
Geophysical research letters, 27(14), 2093-2096 (2002-01-05)
A one-week in situ intercomparison campaign was completed on the Rice University campus for measuring HCHO using three different techniques, including a novel optical sensor based on difference frequency generation (DFG) operating at room temperature. Two chemical derivatization methods, 2,4-dinitrophenylhydrazine
D A Cancilla et al.
Journal of chromatography, 627(1-2), 1-16 (1992-12-25)
A review on the use of O-(2,3,4,5,6-pentafluorophenyl)methylhydroxylamine hydrochloride (PFBHA) for the determination of carbonyl-containing compounds is presented. PFBHA has been used in the determination of such diverse compounds as thromboxane B2, prostaglandins, amygdalin and a variety of other aldehydes, ketones
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