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263532

Sigma-Aldrich

3,5-Difluoroaniline

98%

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About This Item

Linear Formula:
F2C6H3NH2
CAS Number:
372-39-4
Molecular Weight:
129.11
Beilstein:
2802286
EC Number:
206-752-8
MDL number:
MFCD00007763
UNSPSC Code:
12352100
PubChem Substance ID:
24855981
NACRES:
NA.22

Assay

98%

form

solid

mp

37-41 °C (lit.)

functional group

fluoro

SMILES string

Nc1cc(F)cc(F)c1

InChI

1S/C6H5F2N/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2

InChI key

KQOIBXZRCYFZSO-UHFFFAOYSA-N

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General description

In vitro nephrotoxic effects of 3,5-difluoroaniline has been investigated in renal cortical slices obtained from the kidneys of untreated, male Fischer 344 rats.

Application

3,5-Difluoroaniline has been used in the preparation of 3,5-difluorodimethylaniline.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H312 + H332

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

167.0 °F - closed cup

Flash Point(C)

75 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

263532-5G:
263532-BULK:
263532-VAR:
263532-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB4074
BCBP7151V
U20794
14512DE
U18367

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Further studies on the carcinogenicity of dyes related to 4-dimethylaminoazobenzene; the requirement for an unsubstituted 2-position.
J A MILLER et al.
Cancer research, 17(5), 387-398 (1957-06-01)
S K Hong et al.
Toxicology letters, 114(1-3), 125-133 (2000-03-14)
Haloanilines are widely used as chemical intermediates in the manufacture of pesticides, dyes and drugs. The purpose of this study was to examine the in vitro nephrotoxic effects of the four 4-haloaniline and four 3,5-dihaloaniline isomers using renal cortical slices

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