JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Building Blocks
Organic Building Blocks
4-(Trifluoromethyl)aniline - 98%, high purity , CAS No.455-14-1

Skip to the end of the images gallery

Skip to the beginning of the images gallery

4-(Trifluoromethyl)aniline - 98%, high purity , CAS No.455-14-1

2 Citations

COA

Grade & Purity:

≥98%

Cas Number: 455-14-1
Molecular Weight: 161.12
Beilstein Registry Number: 1564853
EC Number: 207-236-5
MDL number: MFCD00064396
PubChem CID: 9964

In stock

Item Number

T100951

Grouped product items
SKU	Size	Availability	Price
T100951-5g	5g	3	$12.90
T100951-25g	25g	2	$29.90
T100951-100g	100g	1	$119.90
T100951-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$419.90

View related series

Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms	XSALEIBQORDDCL-UHFFFAOYSA-N \| .alpha.,.alpha.-Trifluoro-p-anisidine \| 1-amino-4-(trifluoromethyl)benzene \| EC 207-236-5 \| A0662 \| p-Amino-.alpha.,.alpha.,.alpha.-trifluorotoluene \| DTXSID5060013 \| 4-trifluormethylaniline \| Aniline, p-(trifluoromethyl)- \|
Specifications & Purity	≥98%
Storage Temp	Protected from light,Argon charged
Shipped In	Normal
Product Description	It is used in the synthesis of 4-(trialkylmethyl)anilines, and It was also used as a synthetic building block.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Trifluoromethylbenzenes

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Trifluoromethylbenzenes
Intermediate Tree Nodes	Not available
Direct Parent	Trifluoromethylbenzenes
Alternative Parents	Aniline and substituted anilines Primary amines Organopnictogen compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Trifluoromethylbenzene - Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organofluoride - Organohalogen compound - Amine - Alkyl halide - Alkyl fluoride - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups.
External Descriptors	substituted aniline - (trifluoromethyl)benzenes
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	4-(trifluoromethyl)aniline
INCHI	InChI=1S/C7H6F3N/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4H,11H2
InChIKey	ODGIMMLDVSWADK-UHFFFAOYSA-N
Smiles	C1=CC(=CC=C1C(F)(F)F)N
Isomeric SMILES	C1=CC(=CC=C1C(F)(F)F)N
WGK Germany	3
RTECS	XU9260000
PubChem CID	9964
UN Number	3276
Molecular Weight	161.12
Beilstein	1564853
Reaxy-Rn	1564853

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

17 results found

Lot Number	Certificate Type	Date	Item
B2525447	Certificate of Analysis	Feb 15, 2025	T100951
B2525452	Certificate of Analysis	Feb 15, 2025	T100951
B2525450	Certificate of Analysis	Feb 15, 2025	T100951
B2525451	Certificate of Analysis	Feb 15, 2025	T100951
B2525459	Certificate of Analysis	Feb 15, 2025	T100951
I2405217	Certificate of Analysis	Jun 24, 2024	T100951
I2405218	Certificate of Analysis	Jun 24, 2024	T100951
I2405337	Certificate of Analysis	Jun 24, 2024	T100951
K1814096	Certificate of Analysis	Sep 15, 2022	T100951
H1808119	Certificate of Analysis	Jun 15, 2022	T100951
A2214213	Certificate of Analysis	Jan 27, 2022	T100951
C1808059	Certificate of Analysis	Jan 26, 2022	T100951
G2216510	Certificate of Analysis	Jan 13, 2022	T100951
A2429419	Certificate of Analysis	Jan 13, 2022	T100951
G2216509	Certificate of Analysis	Jan 13, 2022	T100951
G2216512	Certificate of Analysis	Jan 13, 2022	T100951
G2216511	Certificate of Analysis	Jan 13, 2022	T100951

Show more⌵

Chemical and Physical Properties

Sensitivity	light &air&moisture&heat sensitive
Refractive Index	1.48
Flash Point(°F)	188.6 °F
Flash Point(°C)	86℃
Boil Point(°C)	83°C
Melt Point(°C)	5-8°C
Molecular Weight	161.120 g/mol
XLogP3	2.400
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	0
Exact Mass	161.045 Da
Monoisotopic Mass	161.045 Da
Topological Polar Surface Area	26.000 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	124.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Jiajie Lyu, Beibei Ji, Nan Wu, Wei Liao, Changping Yin, Shuxin Bai, Suli Xing. (2023) The effect of substituent group in allyl benzoxazine on the thermal, mechanical and dielectric properties of modified bismaleimide. REACTIVE & FUNCTIONAL POLYMERS, 191 (105673).
2. Hong Tu, Ying Xu, Shun-shun Chen, Ya Wang, Sheng-xin Guo, Jian Wu. (2024) Screening of Ultra-Efficient Visible Light Catalysts via Material Modification to Activate Electron Polarization Inside the Material. Advanced Energy and Sustainability Research, (2400175).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.