Skip to Content
Merck
All Photos(1)

Documents

257923

Sigma-Aldrich

Perfluorobutyryl chloride

98%

Synonym(s):

Heptafluorobutyryl chloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CF3CF2CF2COCl
CAS Number:
Molecular Weight:
232.48
Beilstein:
1790269
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

7.22 psi ( 20 °C)

Assay

98%

form

liquid

refractive index

n20/D 1.3 (lit.)

bp

39 °C (lit.)

density

1.556 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(Cl)=O

InChI

1S/C4ClF7O/c5-1(13)2(6,7)3(8,9)4(10,11)12

InChI key

WFELVFKXQJYPSL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Perfluorobutyryl chloride has been used in the preparation of:
  • ethylcellulose perfluorobutyrate, non-thrombogenic novel fluoropolymer for gas-exchange membranes
  • 2-perfluoroalkylbenzothiazole

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

R J Petersen et al.
Transactions - American Society for Artificial Internal Organs, 21, 242-248 (1975-01-01)
A novel fluoropolymer prepared from ethylcellulose by acylation with perfluorobutyryl chloride has been shown to be remarkably non-thrombogenic in vena cava and renal embolus ring implant tests. Gas permeabilities of this fluoropolymer are dufficient to make it highly attractive for
Synthesis of 2-and 2, 5-substituted benzoxazoles and benzothiazoles.
Soloski EJ, et al.
Journal of Fluorine Chemistry, 8(4), 295-304 (1976)

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