Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

248061

Sigma-Aldrich

Octafluoronaphthalene

96%

Synonym(s):

1,2,3,4,5,6,7,8-Octafluoronaphthalene, Perfluoronaphthalene

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

About This Item

Empirical Formula (Hill Notation):
C10F8
CAS Number:
313-72-4
Molecular Weight:
272.09
EC Number:
206-239-9
MDL number:
MFCD00014307
UNSPSC Code:
12352100
PubChem Substance ID:
24854914
NACRES:
NA.22

Quality Level

200

Assay

96%

form

solid

mp

87-88 °C (lit.)

SMILES string

Fc1c(F)c(F)c2c(F)c(F)c(F)c(F)c2c1F

InChI

1S/C10F8/c11-3-1-2(5(13)9(17)7(3)15)6(14)10(18)8(16)4(1)12

InChI key

JDCMOHAFGDQQJX-UHFFFAOYSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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

Amination of octafluoronaphthalene in liquid ammonia: 2, 6-and 2, 7-Diaminohexafluoronaphthalenes selective preparation.
Journal of Fluorine Chemistry, 129(4), 253-260 (2008)
Qimeng Jiang et al.
Polymers, 12(7) (2020-07-28)
Solid acid catalysts generally show the disadvantage of low acid amount and low recycling rate. To solve these problems, corn stalk-based solid acid catalysts were synthesized through carbonization and sulfonation processes in this work. The results showed that besides the
J C Collings et al.
Acta crystallographica. Section C, Crystal structure communications, 57(Pt 7), 870-872 (2001-07-10)
The structure of the title complex, C10F8*C14H10, comprises mixed stacks of alternating diphenylacetylene and octafluoronaphthalene molecules, both lying at inversion centres and parallel to within 8.6 (1) degrees, in contrast with the herring-bone packing observed in crystals of either pure
A phase transformation with no change in space group symmetry; octafluoronaphthalene.
Pawley GS and Dietrich O-W.
Journal of Physics C: Solid State Physics, 8(16), 2549-2549 (1975)
Polycyclic fluoroaromatic compounds. Part XII.[1] The extent of 1-substitution in octafluoronaphthalene.
Burdon J and Rimmington TW.
Journal of Fluorine Chemistry, 27(3), 257-261 (1985)
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