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Merck

52411

Supelco

Heptafluorobutyric acid

suitable for ion chromatography, ≥99.5% (GC)

Sinónimos:

Edman Reagent No. 3, HFBA, Perfluorobutyric acid

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About This Item

Fórmula lineal:
CF3CF2CF2COOH
Número de CAS:
Peso molecular:
214.04
Beilstein/REAXYS Number:
1426882
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NB.21

vapor density

7 (vs air)

Quality Level

vapor pressure

~10 mmHg ( 25 °C)

description

anionic

assay

≥99.5% (GC)

form

liquid

shelf life

limited shelf life, expiry date on the label

technique(s)

ion chromatography: suitable

refractive index

n20/D 1.3 (lit.)

bp

120 °C/755 mmHg (lit.)

density

1.645 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 mg/kg
Ba: ≤0.01 mg/kg
Bi: ≤0.01 mg/kg
Ca: ≤2 mg/kg
Cd: ≤0.01 mg/kg
Co: ≤0.01 mg/kg
Cr: ≤0.01 mg/kg
Cu: ≤0.01 mg/kg
Fe: ≤0.1 mg/kg
K: ≤0.5 mg/kg
Li: ≤0.01 mg/kg
Mg: ≤1 mg/kg
Mn: ≤0.01 mg/kg
Mo: ≤0.01 mg/kg
Na: ≤3 mg/kg
Ni: ≤0.01 mg/kg
Pb: ≤0.01 mg/kg
Sr: ≤0.01 mg/kg
Zn: ≤0.05 mg/kg

SMILES string

OC(=O)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C4HF7O2/c5-2(6,1(12)13)3(7,8)4(9,10)11/h(H,12,13)

InChI key

YPJUNDFVDDCYIH-UHFFFAOYSA-N

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Application

Heptafluorobutyric acid (HFBA) may be used to cleave glycylserine bonds, in an experimental protocol done in order to sequence glycine-rich protein from lizard claw.

Linkage

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Referencia del producto
Descripción
Precios

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1A

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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Sequence of a glycine-rich protein from lizard claw: unusual dilute acid and heptafluorobutyric acid cleavages.
Inglis A
Proteins: Structure, Function, and Genetics, 757-764 (1987)
Jan Busch et al.
Environmental pollution (Barking, Essex : 1987), 158(5), 1467-1471 (2010-01-08)
Polyfluoroalkyl compounds (PFCs) are widely used in industry and consumer products. These products could end up finally in landfills where their leachates are a potential source for PFCs into the aqueous environment. In this study, samples of untreated and treated
Sławomir Wybraniec et al.
Journal of chromatography. A, 1216(41), 6890-6899 (2009-09-08)
Polar betacyanin pigments together with betaxanthins from ripe cactus fruits of Hylocereus polyrhizus (Cactaceae) were fractionated by means of preparative ion-pair high-speed countercurrent chromatography (IP-HSCCC) also using the elution-extrusion (EE) approach for a complete pigment recovery. HSCCC separations were operated
Marta Llorca et al.
The Science of the total environment, 431, 139-150 (2012-06-12)
Water has been identified as one of the main routes of human exposure to perfluoroalkyl substances (PFASs). This work assessed the presence of 21 PFASs along the whole water cycle using a new fast and cost effective analytical method based
A Hagenaars et al.
Chemosphere, 82(5), 764-772 (2010-11-30)
Perfluorinated compounds (PFCs) are a group of anthropogenic chemicals containing diverse functional groups and chain lengths. They are known to be persistent and bioaccumulative explaining their worldwide environmental presence. The toxicological information on these chemicals is still incomplete and insufficient

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