Skip to Content
Merck
CN

368148

4,4′-(Hexafluoroisopropylidene)dianiline

98%

Synonym(s):

2,2-Bis(4-aminophenyl)hexafluoropropane, 4,4′-(Hexafluoroisopropylidene)dianiline

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(CF3)2C(C6H4NH2)2
CAS Number:
1095-78-9
Molecular Weight:
334.26
NACRES:
NA.23
PubChem Substance ID:
24862893
UNSPSC Code:
12162002
MDL number:
MFCD00039146

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C15H12F6N2/c16-14(17,18)13(15(19,20)21,9-1-5-11(22)6-2-9)10-3-7-12(23)8-4-10/h1-8H,22-23H2

SMILES string

Nc1ccc(cc1)C(c2ccc(N)cc2)(C(F)(F)F)C(F)(F)F

InChI key

BEKFRNOZJSYWKZ-UHFFFAOYSA-N

assay

98%

mp

195-198 °C (lit.)

Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKBH4748V
03110PD
19416CF
10313CQ
02304HC

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Tae Soo Jo et al.
Polymers, 11(5) (2019-05-15)
A set of poly(pyridinium) salts containing various diamine moieties, as molecular connectors, and poly(ethyleneglycol)-4-nonylphenyl-3-sulfopropyl ether, thereafter referred to as "Macroion", as the hydrophilic counterion, were prepared by metathesis reaction from the respective precursory tosylated poly(pyridinium)s in methanol. The structure of

Articles

Fluorinated Hyperbranched Polymers

Fluorocarbon polymers exhibit increased thermal stability, hydrophobicity, lipophobicity, and chemical resistance compared to hydrocarbon analogs.

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