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Trifluoroacetamide

Product Name
Trifluoroacetamide
CAS No.
354-38-1
Chemical Name
Trifluoroacetamide
Synonyms
2,2,2-TRIFLUOROACETAMIDE;Acetamide, 2,2,2-trifluoro-;CF3CONH2;Triflouroacetamide;Three-;TRIFLUOROACETAMIDE;2-TriflouroacetaMide;Three fluoroacetaMide;Trifluoroacetamide98%;2,2,2-Trifluoracetamid
CBNumber
CB0291820
Molecular Formula
C2H2F3NO
Formula Weight
113.04
MOL File
354-38-1.mol
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Trifluoroacetamide Property

Melting point:
65-70 °C (lit.)
Boiling point:
162.5 °C (lit.)
Density 
1.4176 (estimate)
bulk density
960kg/m3
Flash point:
162-164°C
storage temp. 
Store below +30°C.
solubility 
460 g/L (20°C)
pka
12.33±0.50(Predicted)
form 
Crystalline Powder or Crystals
color 
White to pale yellow or beige
PH
3.6 (460g/l, H2O, 23℃)
Water Solubility 
460 g/L (20 ºC)
BRN 
1753625
InChIKey
NRKYWOKHZRQRJR-UHFFFAOYSA-N
LogP
0.725 at 23℃ and pH4.83
Dissociation constant
0 at 23℃
CAS DataBase Reference
354-38-1(CAS DataBase Reference)
NIST Chemistry Reference
Acetamide, 2,2,2-trifluoro-(354-38-1)
EPA Substance Registry System
Acetamide, 2,2,2-trifluoro- (354-38-1)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
RIDADR 
1759
WGK Germany 
3
Hazard Note 
Harmful/Irritant
TSCA 
T
HazardClass 
8
PackingGroup 
III
HS Code 
29241900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.14690
Product name
2,2,2-Trifluoroacetamide
Purity
for synthesis
Packaging
10G
Price
$38
Updated
2025/07/31
Sigma-Aldrich
Product number
8.14690
Product name
2,2,2-Trifluoroacetamide
Purity
for synthesis
Packaging
50G
Price
$104
Updated
2025/07/31
Sigma-Aldrich
Product number
144657
Product name
Trifluoroacetamide
Purity
97%
Packaging
25g
Price
$41.23
Updated
2025/07/31
Sigma-Aldrich
Product number
144657
Product name
Trifluoroacetamide
Purity
97%
Packaging
100g
Price
$108.3
Updated
2025/07/31
TCI Chemical
Product number
T0598
Product name
Trifluoroacetamide
Purity
>98.0%(GC)
Packaging
25g
Price
$20
Updated
2025/07/31
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Trifluoroacetamide Chemical Properties,Usage,Production

Chemical Properties

white to pale yellow or beige crystalline powder

Uses

2,2,2-Trifluoroacetamide used in a convenient alternative to the Gabriel synthesis of primary amines from halides by N-alkylation followed by cleavage of the readily-hydrolyzed trifluoroacetyl group and for improved N-alkylation under phase-transfer conditions allowing successive alkylation with different alkyl groups.

Application

Trifluoroacetamide was used as probe for determination of membrane potential and extra/intracellular volume of erythrocytes by fluorine-19 NMR studies.

Preparation

One-pot synthetic approach to produce trifluoroacetamide has been developed using an electrochemical method with the B12 complex as a catalyst under mild conditions, in open air at room temperature. Thirty examples of trifluoroacetamide were synthesized from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) in moderate to good yields. This user-friendly strategy is compatible with a broad range of trifluoroacetamide syntheses.
10.1142/S1088424621500292

General Description

Trifluoroacetamide is a good quencher of tryptophan fluorescence.

Synthesis

383-63-1

354-38-1

Example 5: Synthesis of the blocking isomer trifluoroacetamide 3a The block trans isomer 2a (0.93 g, 1.84 mmol, 503.4 g/mol) as a sulfate was dissolved in 15 mL of ethanol. Under argon protection, triethylamine (1.8 mL, 13 mmol) and ethyl trifluoroacetate (2.2 mL, 18 mmol) were slowly added (Figure 2a). The reaction mixture was stirred for 2.5 h at room temperature. Upon completion of the reaction, the volatiles were removed by distillation under reduced pressure. The resulting residue was dissolved in 300 mL of ethyl acetate and washed sequentially with 2 x 50 mL of 5% hydrochloric acid solution. The organic phase was dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to afford block-transfer isomerized trifluoroacetamide 3a as an orange solid (0.92 g, 100% yield, 501.4 g/mol). 1H NMR (methanol-d4) δ 8.35 (1H, d); 8.15 (1H, d); 7.80 (1H, s); 6.82 (1H, s); 6.65 (4H, m); 4.82 (2H, s).

References

[1] Patent: US6448407, 2002, B1
[2] Journal of the American Chemical Society, 1943, vol. 65, p. 1459
[3] Journal of the American Chemical Society, 1943, vol. 65, p. 1459
[4] Journal of Organic Chemistry, 1959, vol. 24, p. 1256,1258
[5] Bulletin de la Classe des Sciences, Academie Royale de Belgique, 1922, vol. <5>8, p. 346

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View Lastest Price from Trifluoroacetamide manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
Trifluoroacetamide 354-38-1
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2025-03-10
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Trifluoroacetamide 354-38-1
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 ton
Release date
2024-11-29
Henan Aochuang Chemical Co.,Ltd.
Product
Trifluoroacetamide 354-38-1
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-10-09

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