2,3,4-trifluoroaniline

C6H4F3N

CAS3862-73-5
GHS07 Gefahrensymbol: Gesundheitsschädlich/Reizend – Ausrufezeichen
GHS08 Gefahrensymbol: Gesundheitsgefahr – Gesundheitsgefahr
GHS05 Gefahrensymbol: Ätzend – Ätzwirkung
GHS09 Gefahrensymbol: Umweltgefährlich – Umwelt
Danger

Consulting for 2,3,4-trifluoroaniline

Our experts support you with application, dosage, and compliance.

Request Consultation

Identification

CAS Number
3862-73-5
EC Number
407-170-9
UN Number
3082
Index Number
612-187-00-1
PubChem CID
77468

Physical-chemical properties

Molecular Formula
C6H4F3N
Molar Mass
147.10 g/mol
IUPAC Name
2,3,4-trifluoroaniline

Chemical Identifiers

InChI
InChI=1S/C6H4F3N/c7-3-1-2-4(10)6(9)5(3)8/h1-2H,10H2
InChI Key
WRDGNXCXTDDYBZ-UHFFFAOYSA-N

Overview

2,3,4-trifluoroaniline (CAS 3862-73-5) is a fluorinated aromatic amine compound with enhanced chemical stability and specialized industrial applications. This highly specialized fluorinated aromatic compound represents an important intermediate in pharmaceutical and agrochemical synthesis. With three fluorine substituents positioned at the 2, 3, and 4 positions of the aniline ring, 2,3,4-trifluoroaniline exhibits unique chemical properties that make it valuable for advanced chemical manufacturing processes. The compound's molecular structure, featuring both amino and multiple fluorine functionalities, provides exceptional reactivity patterns essential for complex organic synthesis. The presence of multiple fluorine atoms significantly influences the compound's electronic properties and chemical behavior compared to conventional anilines. This fluorinated structure enhances stability while providing specific reactivity patterns required in pharmaceutical intermediate synthesis. Unlike simpler aromatic compounds such as benzene-1,4-diol, the trifluorinated aniline structure offers superior resistance to metabolic degradation and improved bioavailability in pharmaceutical applications. Safety considerations are paramount when handling 2,3,4-trifluoroaniline, as it is classified under multiple hazard categories including acute toxicity, skin irritation, and eye damage. The compound requires appropriate personal protective equipment and proper ventilation systems during handling and processing. Its classification as ADR Class 9 necessitates specialized transportation and storage protocols. Primary industrial applications include pharmaceutical intermediate synthesis, particularly in the development of fluorinated drug compounds, agrochemical manufacturing for advanced pesticide formulations, and specialty chemical production for high-performance materials. The compound's unique reactivity profile makes it especially valuable in synthesizing complex fluorinated heterocycles. OYSI maintains reliable supply chains for 2,3,4-trifluoroaniline to support European chemical manufacturing requirements.

Safety & Classification

Danger
Classification:

Acute Tox. 4 *; Acute Tox. 4 *; STOT RE 2 *; Skin Irrit. 2; Eye Dam. 1; Aquatic Chronic 2

HHazard Statements (H-Statements)

Describe the nature and severity of the hazard

H312

Harmful in contact with skin.

H302

Harmful if swallowed.

H373

May cause damage to organs through prolonged or repeated exposure.

H315

Causes skin irritation.

H318

Causes serious eye damage.

H411

Toxic to aquatic life with long lasting effects.

Classification according to CLP Regulation (EC) No 1272/2008. The complete list of hazard and precautionary statements can be found in the Safety Data Sheet (SDS).

First Aid Measures

Skin Contact

Harmful

Measures if substance contacts the skin

First Aid Actions

  • +P302IF ON SKIN:
  • +P352Wash with plenty of water.
  • +P361Take off immediately all contaminated clothing.
  • +P313Get medical advice/attention.

Related hazard statements:

Eye Contact

Harmful

Measures if substance gets into the eyes

First Aid Actions

  • +P305IF IN EYES:
  • +P351Rinse cautiously with water for several minutes.
  • +P338Remove contact lenses, if present and easy to do. Continue rinsing.
  • +P313Get medical advice/attention.

Related hazard statements:

Ingestion

Harmful

Measures if substance is accidentally swallowed

First Aid Actions

  • +P301IF SWALLOWED:
  • +P330Rinse mouth.
  • +P331Do NOT induce vomiting.
  • +P310Immediately call a POISON CENTER/doctor.

Related hazard statements:

General Measures

Emergency 112 | Poison Control: +49 30 19240 (DE), +33 1 45 42 59 59 (FR), +31 30 274 88 88 (NL)

First aid measures are based on CLP classification and associated P-statements. They do not replace the Safety Data Sheet (SDS). In case of emergency, always consult the full SDS and a physician.

Transport (ADR)

UN Number3082
ADR Class9
Packing GroupIII
Tunnel Code-
Proper Shipping Name2,3,4-Trifluoranilin
Marine PollutantNo

Frequently Asked Questions

What is 2,3,4-trifluoroaniline?

2,3,4-trifluoroaniline is an organofluorine compound with the molecular formula C6H4F3N and CAS number 3862-73-5. This aromatic amine features three fluorine atoms substituted on positions 2, 3, and 4 of the aniline ring. With a molecular weight of 147.1 g/mol, it belongs to the class of fluorinated aromatic amines used primarily as chemical intermediates in pharmaceutical and agrochemical synthesis.

What are the physicochemical properties of 2,3,4-trifluoroaniline?

2,3,4-trifluoroaniline is typically a colorless to pale yellow liquid or crystalline solid at room temperature. The presence of three fluorine atoms significantly influences its physical properties, including increased stability and altered solubility compared to unsubstituted aniline. The compound exhibits moderate volatility and has distinct chemical reactivity due to the electron-withdrawing effects of the fluorine substituents on the aromatic ring.

What is 2,3,4-trifluoroaniline used for?

2,3,4-trifluoroaniline is primarily used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique substitution pattern makes it valuable for producing fluorinated compounds with specific biological activities. The compound serves as a building block in medicinal chemistry for developing drugs and in agricultural chemistry for creating pesticides and herbicides where fluorine incorporation enhances efficacy and metabolic stability.

How to handle 2,3,4-trifluoroaniline safely?

2,3,4-trifluoroaniline requires careful handling due to its classification as Acute Tox. 4, Skin Irrit. 2, and Eye Dam. 1. Essential personal protective equipment includes chemical-resistant gloves, safety goggles or face shield, and appropriate respiratory protection. Work should be conducted in well-ventilated areas or under fume hoods. Avoid skin and eye contact, and prevent inhalation of vapors. Emergency eyewash stations and safety showers should be readily accessible.

How to store 2,3,4-trifluoroaniline correctly?

2,3,4-trifluoroaniline should be stored in tightly sealed containers in a cool, dry, well-ventilated area away from heat sources and direct sunlight. The storage area must be designed to contain spills and prevent environmental release due to its Aquatic Chronic 2 classification. Keep away from incompatible materials such as strong oxidizing agents and acids. Ensure proper labeling with GHS pictograms and maintain appropriate inventory records.

What to do in case of contact with 2,3,4-trifluoroaniline?

Immediate action is required for any contact with 2,3,4-trifluoroaniline due to its corrosive and toxic properties. For eye contact, flush immediately with copious amounts of water for at least 15 minutes and seek medical attention. For skin contact, remove contaminated clothing and wash thoroughly with soap and water. If inhaled, move to fresh air immediately. In case of ingestion, do not induce vomiting and seek immediate medical attention.

How to dispose of 2,3,4-trifluoroaniline appropriately?

2,3,4-trifluoroaniline disposal must comply with local and international hazardous waste regulations due to its toxic and environmentally hazardous properties. The compound cannot be disposed of in regular waste streams and requires treatment by licensed hazardous waste disposal facilities. Incineration at appropriate temperatures or chemical neutralization may be suitable methods. Always consult with waste management professionals and follow applicable environmental regulations including REACH requirements.

How to transport 2,3,4-trifluoroaniline?

2,3,4-trifluoroaniline is classified as ADR Class 9 (Miscellaneous Dangerous Substances), Packing Group III for transportation. This classification requires appropriate packaging, labeling, and documentation according to international dangerous goods regulations. Vehicles must carry proper placards and emergency response information. Drivers require ADR training certification, and shipments must include proper shipping names, UN numbers, and hazard labels. Professional logistics providers experienced with chemical transport should be utilized.

Is 2,3,4-trifluoroaniline subject to specific regulations?

2,3,4-trifluoroaniline is subject to comprehensive chemical regulations including REACH registration requirements in Europe and CLP classification obligations. While not currently listed as an SVHC, its toxic properties require compliance with occupational health and safety regulations, environmental protection laws, and proper chemical inventory reporting. Industrial users must maintain safety data sheets, conduct risk assessments, and implement appropriate control measures according to regulatory requirements.

Where to buy 2,3,4-trifluoroaniline in Europe?

2,3,4-trifluoroaniline is available through OYSI, a specialized European distributor of technical chemicals serving industrial and research customers across Europe. OYSI provides reliable supply chains, proper documentation, and regulatory compliance support for chemical purchases. Professional buyers can contact OYSI directly to discuss specific requirements, quantities, and delivery options. All products come with appropriate safety documentation and regulatory compliance certificates required for industrial applications.

Data Sources

Classification per CLP Regulation (EC) No 1272/2008. Data from ECHA and PubChem.