MilliporeSigma
All Photos(3)

Documents

224936

Sigma-Aldrich

4-(Trifluoromethyl)aniline

99%

Sign Into View Organizational & Contract Pricing

Synonym(s):
α,α,α-Trifluoro-p-toluidine, 4-Aminobenzotrifluoride
Linear Formula:
CF3C6H4NH2
CAS Number:
Molecular Weight:
161.12
Beilstein/REAXYS Number:
1564853
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.483 (lit.)

bp

83 °C/12 mmHg (lit.)

density

1.283 g/mL at 25 °C (lit.)

SMILES string

Nc1ccc(cc1)C(F)(F)F

InChI

1S/C7H6F3N/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4H,11H2

InChI key

ODGIMMLDVSWADK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
337056A41607A41801
4-(Trifluoromethyl)aniline 99%

224936

4-(Trifluoromethyl)aniline

4-(Trifluoromethoxy)aniline 98%

337056

4-(Trifluoromethoxy)aniline

2-(Trifluoromethyl)aniline 99%

A41607

2-(Trifluoromethyl)aniline

3-(Trifluoromethyl)aniline ≥99%

A41801

3-(Trifluoromethyl)aniline

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

refractive index

n20/D 1.483 (lit.)

refractive index

n20/D 1.463 (lit.)

refractive index

n20/D 1.481 (lit.)

refractive index

n20/D 1.480 (lit.)

bp

83 °C/12 mmHg (lit.)

bp

73-75 °C/10 mmHg (lit.)

bp

170-173 °C (lit.), 68 °C/15 mmHg (lit.)

bp

187 °C (lit.)

density

1.283 g/mL at 25 °C (lit.)

density

1.32 g/mL at 20 °C (lit.)

density

1.282 g/mL at 25 °C (lit.)

density

1.29 g/mL at 25 °C (lit.)

form

liquid

form

liquid

form

liquid

form

liquid

Application

4-(Trifluoromethyl)aniline was used in the synthesis of 4-(trialkylmethyl)anilines. It was also used as a synthetic building block.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

ppe

Eyeshields, Faceshields, Gloves, 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?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 3

1 of 3

Tetrahedron Letters, 48, 4749-4749 (2007)
Meritxell Guinó et al.
The Journal of organic chemistry, 72(16), 6290-6293 (2007-07-13)
Optically active torcetrapib was synthesized in seven steps from achiral precursors without the need for protecting groups, utilizing an enantioselective aza-Michael reaction to achieve asymmetry.
A Facile Synthesis of 4-(Trialkylmethyl) anilines by the Reaction of 4-(Trifluoromethyl) aniline with Grignard Reagents.
Synthetic Communications, 27(11), 1975-1980 (1997)
Giorgio Mangiarotti
Biochemistry and cell biology = Biochimie et biologie cellulaire, 80(2), 261-270 (2002-05-07)
Ribosomal protein mRNAs left over from growth are selectively excluded from polyribosomes in the first half of Dictyostelium discoideum development. This is due to the fact that they are sequestered by a class of free 40S ribosomal subunits, characterized by
S H Coleman et al.
Journal of general microbiology, 139(4), 707-716 (1993-04-01)
The rpmB,G operon of Escherichia coli codes for the synthesis of ribosomal proteins L28 and L33. In one mutant strain (TP28), these two proteins are made at about half their normal rates, ribosome assembly is greatly perturbed and precursor particles

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