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Trifluoroacetic anhydride

CAS No.
407-25-0
Chemical Name:
Trifluoroacetic anhydride
Synonyms
TFAA;trifluoroacetic;2,2,2-Trifluoroacetic anhydride;TRIFLUOROACETIC ACID ANHYDRIDE;TRIFLUORACETIC ANHYDRIDE;Trifluoroacetic anhy;TIFLUOROACETIC ANHYDRIDE;trimethylamine (TMA);uoroacetic anhydride;TRIFLUOROACETO ANHYDRIDE
CBNumber:
CB6853606
Molecular Formula:
C4F6O3
Molecular Weight:
210.03
MDL Number:
MFCD00000416
MOL File:
407-25-0.mol
MSDS File:
SDS
Last updated:2024-11-22 13:52:42

Trifluoroacetic anhydride Properties

Melting point -65 °C (lit.)
Boiling point 39.5-40 °C (lit.)
Density 1.511 g/mL at 20 °C (lit.)
vapor pressure 6.28 psi ( 20 °C)
refractive index n20/D 1.3(lit.)
Flash point -26 °C
storage temp. 2-8°C
solubility Miscible with benzene, dichloromethane, diethyl ether, dimethylformamide, terahydrofuran and acetonitrile.
form Liquid
pka 0.43[at 20 ℃]
Specific Gravity 1.487
color Clear
Water Solubility Hydrolysis
Sensitive Moisture Sensitive
BRN 746197
Stability Stable, but moisture sensitive. Reacts with water to liberate hydrogen (flammable!). Incompatible with water, strong oxidizing agents.
LogP 0.79 at 25℃
CAS DataBase Reference 407-25-0(CAS DataBase Reference)
FDA UNII 5ENA87IZHT
NIST Chemistry Reference Acetic acid, trifluoro-, anhydride(407-25-0)
EPA Substance Registry System Acetic acid, trifluoro-, anhydride (407-25-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
Signal word  Danger
Hazard statements  H314-H332-H412
Precautionary statements  P273-P280-P301+P330+P331-P303+P361+P353-P304+P340+P312-P305+P351+P338+P310
Hazard Codes  C,T
Risk Statements  14-20-35-52/53-34-23/24/25
Safety Statements  26-36/37/39-43-45-61-9-8-28A-27
RIDADR  UN 3265 8/PG 1
WGK Germany  2
RTECS  AJ9800000
3-10
Hazard Note  Corrosive/Moisture Sensitive
TSCA  T
HazardClass  8
PackingGroup  I
HS Code  29159080
Toxicity skn-rbt 500 mg/24H SEV 28ZPAK -,91,72
NFPA 704
0
3 1

Trifluoroacetic anhydride price More Price(56)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.08261 Trifluoroacetic anhydride for synthesis 407-25-0 25mL $43.7 2024-03-01 Buy
Sigma-Aldrich 8.08261 Trifluoroacetic anhydride for synthesis 407-25-0 100mL $114 2024-03-01 Buy
Sigma-Aldrich 106232 Trifluoroacetic anhydride ReagentPlus , ≥99% 407-25-0 10x1g $212 2024-03-01 Buy
Sigma-Aldrich 8.08261 Trifluoroacetic anhydride for synthesis 407-25-0 500mL $456 2024-03-01 Buy
Sigma-Aldrich 106232 Trifluoroacetic anhydride ReagentPlus , ≥99% 407-25-0 3kg $1460 2024-03-01 Buy
Product number Packaging Price Buy
8.08261 25mL $43.7 Buy
8.08261 100mL $114 Buy
106232 10x1g $212 Buy
8.08261 500mL $456 Buy
106232 3kg $1460 Buy

Trifluoroacetic anhydride Chemical Properties,Uses,Production

Description

Trifluoroacetic acid anhydride (TFAA), a perfluoroacylated acylation reagent, forms stable, volatile derivatives with alcohols, amines, and phenols. 

Chemical Properties

Clear, colorless liquid

Uses

Trifluoroacetic anhydride is used for the introduction of trifluoroacetyl group in organic synthesis. It is involved in the preparation of N- and O-trifluoroacetyl derivatives of a wide range of biologically active compounds for gas chromatography analysis. It plays an important role as desiccant for trifluoroacetic acid. It is also used in the oxidation of aldehydes to acids, esters, amides as well as in the protection of alcohols and amines. In addition, it is used as analytical reagents, solvents and dehydration condensing agent. It serves as an intermediate of fluorine fine chemicals, pharmaceuticals and agrochemicals.

Uses

Used as analytical reagents, solvents, catalysts, dehydration condensing agent, protection agent of trifluoroacetylation of carboxyl and amino; used as Intermediate of fluorine fine chemicals, pharmaceutical, agrochemical.

Preparation

Trifluoroacetic anhydride is prepared by reaction of trifluoroacetyl chloride with an alkali metal or alkaline-earth metal salt of trifluoroacetic acid at approximately 50° C. 

Safety Profile

A severe skin and eye irritant.Explosive reaction with dimethyl sulfoxide; nitric acid +1,3,5-triazine (at 36°C); nitric acid + 1,3,5-triacetylhexahydro-1,3,5-triazine (at 30°C). Incompatiblewith lithium tetrahydroaluminate. When heated todecomposit

Purification Methods

Purification by distilling over KMnO4, as for the acid above, is EXTREMELY DANGEROUS due to the possiblility of EXPLOSION. It is best purified by distilling from P2O5 slowly, and collecting the fraction boiling at 39.5o. Store it in a dry atmosphere. Highly TOXIC vapour and attacks skin, work in an efficient fume hood. [Beilstein 2 IV 469.]

76-05-1
407-25-0
Synthesis of Trifluoroacetic anhydride from Trifluoroacetic acid

Trifluoroacetic anhydride Preparation Products And Raw materials

Raw materials

Preparation Products

1of8

Global( 549)Suppliers
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CD Chemical Group Limited
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View Lastest Price from Trifluoroacetic anhydride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Trifluoroacetic anhydride pictures 2024-11-26 Trifluoroacetic anhydride
407-25-0
US $0.00 / KG 1KG 99% 500mt Jinan Finer Chemical Co., Ltd
Trifluoroacetic anhydride pictures 2024-11-13 Trifluoroacetic anhydride
407-25-0
US $19.90 / kg 1kg 99% 10 mt Hebei Weibang Biotechnology Co., Ltd
Trifluoroacetic Anhydride pictures 2024-10-11 Trifluoroacetic Anhydride
407-25-0
US $10.00 / KG 1KG 99.7% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
TRIFLUOROACETO ANHYDRIDE Trifluoroacetic acid anhydride (TFAH) RIFLUOROACETIC ANHYDRIDE Trifluoroacetic anhydride 10g [407-25-0] Trifluoroacetic anhydride, min. 98% trifluoroacetyl 2,2,2-trifluoroacetate Trifluoroacetic anhydride, 99+% 100GR Trifluoroacetic anhydride, 99+% 25GR Trifluoracetic anhydride, min. 98% Bis(2,2,2-trifluoroacetic acid)anhydride Bis(trifluoroacetic acid) anhydride Di(trifluoroacetic)anhydride Trifluoroacetyltrifluoroacetate Trifluoroethanoicanhydride TRIFLUOROACETIC ANHYDRIDE BIS(TRIFLUOROACETIC) ANHYDRIDE Triflyuoroacetic anhydride Aceticacid,trifluoro-,anhydride Anhydrid kyseliny trifluoroctove anhydridkyselinytrifluoroctove Hexafluoroacetic anhydride hexafluoroaceticanhydride Perfluoroacetic anhydride perfluoroaceticanhydride TRIFLUOROACETIC ANHYDRIDE, REAGENTPLUS, >=99% TRIFLUOROACETIC ANHYDRIDE, DERIVATIZA-TI ON REAGENT TRIFLUOROACETIC ANHYDRIDE REAGENTPLUS(& TrifluoroaceticAnhydride/Tfaa/Tfah/Trifluoroaceticanhydride TrifluoroaceticAnhydride/Tfaa Trifluoroacetic anhydride, 99+% Trifluoraceticanhydride,min.98% TRIFLUOROACETICANHYDRIDE,REAGENT Trifluoressigsureanhydrid Perfluoracetic anhydride TRIFLUOROACETIC ANHYDRIDE: 99.5% TRIFLUOROACETIC ANHYDRIDE FOR SYNTHESIS TRIFLUOROACETIC ANHYDRIDE FOR GAS CHROMA Trifluoroacetic anhydride 99% TRIFLUOROACETIC ANHYDRINE TFAH)Trifluoroacetic anhyd 1,1,1,5,5,5-Hexafluoro-3-oxapentan-2,4-dione, Perfluoro(3-oxapentan-2,4-dione), 2,2,2-Trifluoroethanoic anhydride Aceticacid, 2,2,2-trifluoro-, 1,1'-anhydride Three fluorineacetic anhydride trimethylamine (TMA) Trifluoroacetic anhydride ReagentPlus(R), >=99% Trifluoroacetyl 2,2,2-trifluoroacetate (Trifluoroacetic anhydride) Trifluoroacetic anhydride≥ 99% (GC) TFAA Trifluoroacetic acid anhydride trifluoro-aceticacianhydride Trifluoroacetyl anhydride trifluoroacetylanhydride Trifluoroacetic Anhydride > Trifluoroacetic Anhydride (Reagent), Fisher Chemical Trifluoroacetic Anhydride, 99&plus uoroacetic anhydride Trifluoroacetic anhydride 407-25-0 fiona trifluorocytic anhydride fiona TRIFLUOROACETIC ANHYDRIDE, 99%TRIFLUOROACETIC ANHYDRIDE, 99%TRIFLUOROACETIC ANHYDRIDE, 99%TRIFLUOROACETIC ANHYDRIDE, 99%