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3-三氟甲基苯胺

3-Aminotrifluorotoluene

CAS: 98-16-8

Molecular Formula: C7H6F3N

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3-三氟甲基苯胺 - Names and Identifiers

Name 3-Aminotrifluorotoluene
Synonyms CGA 72903
3-Trifluormethylanilin
m-aminobenzotrifluoride
3-aminobenzotrifluoride
3-Aminotrifluorotoluene
3-Trifluoromethylaniline
3-(Trifluoromethyl)aniline
META-AMINOBENZOTRIFLUORIDE
3-(Trifluoromethyl)Aniline
M-(Trifluoromethyl)aniline
META-TRIFLUOROMETHYLANILINE
META-AMINOBENZOLTRIFLUORIDE
3-(TRIFLUOROMETHYL)BENZAMINE
3-(trifluoromethyl)benzenamine
3-(Trifluoromethyl)phenylamine
alpha,alpha,alpha-trifluoro-m-toluidine
3-amino-alpha,alpha,alpha-trifluorotoluene
CAS 98-16-8
EINECS 202-643-4
InChI InChI=1/C7H6F3N/c8-7(9,10)5-2-1-3-6(11)4-5/h1-4H,11H2
InChIKey VIUDTWATMPPKEL-UHFFFAOYSA-N

3-三氟甲基苯胺 - Physico-chemical Properties

Molecular FormulaC7H6F3N
Molar Mass161.12
Density1.29 g/mL at 25 °C(lit.)
Melting Point5 °C
Boling Point187°C(lit.)
Flash Point185°F
Water Solubility5 g/L (20 ºC)
Solubility 5 g/L (20°C)
Vapor Presure0.3 mm Hg ( 20 °C)
AppearanceLiquid
Specific Gravity1.290
ColorClear light yellow
Exposure LimitACGIH: TWA 2.5 mg/m3NIOSH: IDLH 250 mg/m3
BRN387672
pKa3.49(at 25℃)
Storage ConditionStore below +30°C.
Refractive Indexn20/D 1.480(lit.)
Physical and Chemical PropertiesThis product is colorless and transparent liquid, m.p.5 ~ 6 ℃, B. p.187 ℃,n20D 1.4800, relative density 1.290,f.p.85 ℃, soluble in ethanol, toluene, benzene and other solvents.
UseMainly used as pharmaceutical, pesticide, dye intermediates

3-三氟甲基苯胺 - Risk and Safety

Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R33 - Danger of cumulative effects
R23 - Toxic by inhalation
R21/22 - Harmful in contact with skin and if swallowed.
R26 - Very Toxic by inhalation
R24 - Toxic in contact with skin
R22 - Harmful if swallowed
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S28A -
UN IDsUN 2948 6.1/PG 2
WGK Germany2
RTECSXU9180000
TSCAT
HS Code29214300
Hazard NoteToxic/Irritant
Hazard Class6.1
Packing GroupII

3-三氟甲基苯胺 - Nature

Open Data Verified Data

colorless oily liquid with a taste as aniline. The boiling point is 187.5 ℃, the relative density is 1.30467 (12.5 ℃), and the refractive index is 1. 482~1. 486 (12.5 ℃). Insoluble in water, soluble in alcohol, ether. It turned brown when exposed to photo-oxidation. It can react with sodium nitrite to generate diazonium salt, and then can be made into a series of derivatives.

Last Update:2024-01-02 23:10:35

3-三氟甲基苯胺 - Preparation Method

Open Data Verified Data

obtained by reduction of M-nitrotoluene trifluoride.

Last Update:2022-01-01 10:51:20

3-三氟甲基苯胺 - Use

Open Data Verified Data

currently used for the preparation of antipsychotic drugs fluphenazine, trifluoperazine, trifluorobutylene, etc.; Also used in the synthesis of herbicides flumidone, fludrodone, Nor-flurazon, etc, for controlling broad-leaved weeds and perennial weeds such as wheat and cotton fields.

Last Update:2022-01-01 10:51:19

3-三氟甲基苯胺 - Safety

Open Data Verified Data
  • This product decomposes toxic smoke by heat. Inhalation, skin absorption, digestive tract into the cause of poisoning.
  • The packaging shall be made of glass bottles and wooden cases with inner lining of bedding or iron drum. Store in a cool, ventilated warehouse. Keep away from the fire, heat source, avoid direct sunlight; And edible raw materials Isolation of the storage and transportation; Handling light light unloading, to prevent damage to the container.
Last Update:2022-01-01 10:51:20

3-三氟甲基苯胺 - Reference Information

LogP2.09-2.16 at 25-30℃ and pH5.9
surface tension 64.5mN/m at 1g/L and 22.2 ℃
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
preparation of M-bromotrifluorotoluene 1. Direct bromination of trifluoromethylbenzene the yield of this method was 80%. Raw material consumption quota: Trifluoromethyl benzene (≥ 98%)686kg/t, bromine 1142kg/t, iron powder 200kg/t. 2. By M-amino trifluorotoluene diazotization, substitution derived. M-aminotrifluorotoluene was slowly added to hydrobromic acid with stirring at a temperature not exceeding 50 °c. After cooling, sodium nitrite solution was added and the temperature was controlled below 10 °c until the end of diazotization. The diazo solution was added to a boiled solution of cuprous bromide and hydrobromic acid and water vapor distillation was initiated to distill the organic matter with water vapor. The distillate was layered, and the organic layer was taken, washed with concentrated sulfuric acid, washed with water and dilute alkali solution, and washed with water until neutral. The oil layer was dehydrated with anhydrous calcium chloride, filtered and distilled under reduced pressure to collect fraction at 73-74.5 ℃(6.0kPa) to obtain m-bromotrifluorotoluene.
Use 3-trifluoromethylaniline is an intermediate of the herbicides fluron, Fluridone and pyrifluoroaniline, it is also a pharmaceutical intermediate, such as for the synthesis of butyl fluoride acid, fluoride Ester, fluphenazine, trifluoropromazine, fluorine and so on.
dyes, important intermediates for pharmaceuticals and pesticides. For the manufacture of antipsychotic drugs fluphenazine, triflurazol, trifluorobutylene and so on. It is used in the synthesis of herbicides such as fluoridone, fluororotone, Norflurazon, etc., for controlling broad-leaved weeds and perennial weeds such as wheat fields and cotton fields.
mainly used as pharmaceutical, pesticide, dye intermediates
production method reduction of M-nitrobenzotrifluoride with iron powder: hydrochloric acid and iron powder were sequentially added into water and heated to 80 ℃, slowly add M-nitrotrifluorotoluene Dropwise, control it at 80-85 ℃, raise the temperature to reflux within 10% H, keep the temperature for 3H, cool to 50 ℃, add 1.7 times of sodium carbonate solution (), distill, the distillate was separated from the aqueous layer, and the oil was dried over anhydrous sodium sulfate and filtered to obtain meta-amino trifluorotoluene. The yield was 85.7%.
The preparation method is to add M-trifluoromethyl nitrobenzene, solvent ethanol and catalyst in sequence in the autoclave, replace the air in the autoclave with nitrogen, then start stirring, and enter hydrogen gas, keep the pressure in the kettle at about 0.1 MPa, control the temperature at (100±5)℃, react until hydrogen is not absorbed, and the reaction time is about 1 h, and cool with cooling water, the temperature in the kettle was lowered to below 40 ° C., the residual pressure in the kettle was used to discharge the material, the reaction solution was filtered, the catalyst was removed, the solvent and water were distilled off under normal pressure, and the product was distilled under reduced pressure.
category toxic substances
toxicity grade high toxicity
Acute toxicity oral-rat LD50: 480 mg/kg; Oral-mouse LD50: 220 mg/kg
flammability hazard characteristics open flame flammable; Thermal decomposition releases toxic aniline, nitrogen oxides and fluoride gases
storage and transportation characteristics The warehouse is ventilated and dried at low temperature; It is stored and transported separately from food raw materials
fire extinguishing agent carbon dioxide, sand, foam, water
Occupational Standard SEL 0.5 mg/m3
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 20:49:11
3-三氟甲基苯胺
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