Skip to Content
MilliporeSigma
All Photos(1)

Documents

77249

Sigma-Aldrich

Heptafluorobutyric acid

≥99.0% (GC)

Synonym(s):

Edman Reagent No. 3, HFBA, Perfluorobutyric acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CF3CF2CF2COOH
CAS Number:
375-22-4
Molecular Weight:
214.04
Beilstein/REAXYS Number:
1426882
EC Number:
206-786-3
MDL number:
MFCD00004171
UNSPSC Code:
12352106
PubChem Substance ID:
57652682
NACRES:
NA.26

vapor density

7 (vs air)

Quality Level

100

vapor pressure

~10 mmHg ( 25 °C)

assay

≥99.0% (GC)

form

liquid

analyte chemical class(es)

amino acids

refractive index

n20/D 1.3 (lit.)

bp

120 °C/755 mmHg (lit.)

density

1.645 g/mL at 25 °C (lit.)

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

Looking for similar products? Visit Product Comparison Guide

Other Notes

In protein sequencing with converted Beckman gas-liquid phase sequencer

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

A S Bhown et al.
Analytical biochemistry, 175(1), 39-51 (1988-11-15)
As an effective aid to extend the microsequencing capabilities the Beckman protein/peptide sequenator Series 890C has been successfully converted to a gas-liquid system, in which coupling buffer 25% trimethylamine was employed as a gas, and heptafluorobutyric acid as a liquid.
Ulrika Eriksson et al.
Environmental science and pollution research international, 20(11), 7940-7948 (2013-04-17)
Diet and drinking water are suggested to be major exposure pathways for perfluoroalkyl substances (PFASs). In this study, food items and water from Faroe Islands sampled in 2011/2012 were analyzed for 11 perfluoroalkyl carboxylic acids (PFCAs) and 4 perfluoroalkane sulfonic
V Gellrich et al.
Chemosphere, 87(9), 1052-1056 (2012-03-07)
Perfluorinated compounds (PFCs) can be detected worldwide in both, soil and water. In order to study the leaching behavior of this heterogeneous group of compounds in soil, flow-through column experiments have been conducted. Ten perfluoro carboxylates and four perfluoro sulfonates
Merja R Häkkinen et al.
Journal of pharmaceutical and biomedical analysis, 45(4), 625-634 (2007-10-20)
A reversed phase liquid chromatography-electrospray ionization-tandem mass spectrometric method (RP-LC-ESI-MS/MS) was developed to separate and detect polyamines with minimal sample pre-treatment and without any derivatization. Prior to MS/MS analysis, a complete chromatographic separation of polyamines was achieved by a linear
Kaberi P Das et al.
Toxicological sciences : an official journal of the Society of Toxicology, 105(1), 173-181 (2008-05-31)
Perfluorobutyrate (PFBA) is a perfluoroalkyl acid (PFAA) found in the environment. Previous studies have indicated developmental toxicity of PFAAs (perfluorooctane sulfonate [PFOS] and perfluorooctanoate [PFOA]); the current study examines that of PFBA. PFBA/NH4(+) was given to timed-pregnant CD-1 mice by
View All Related Papers

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