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Colorless Liquid Trifluoroacetic Acid CAS 76-05-1 Fine Chemical Products

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 76-05-1

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Plastic bottles, Plastic buckets

Delivery Time: 7-15 days

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CAS 76-05-1 fine chemical products

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Trifluoroacetic Acid CAS 76-05-1

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Colorless liquid Trifluoroacetic Acid

CAS No::
76-05-1
Appearance::
Colorless Liquid
Molecular Formula::
C2HF3O2
Molecular Weight::
114.02
EINECS NO: 200-929-3:
X200-929-3
MDL NO.::
MFCD00004169
CAS No::
76-05-1
Appearance::
Colorless Liquid
Molecular Formula::
C2HF3O2
Molecular Weight::
114.02
EINECS NO: 200-929-3:
X200-929-3
MDL NO.::
MFCD00004169
Colorless Liquid Trifluoroacetic Acid CAS 76-05-1 Fine Chemical Products

Product Description:

Product Name:Trifluoroacetic acid CAS 76-05-1

 

Synonyms:

R3, TRIFLUOROACETIC ACID;

R4A, TRIFLUOROACETIC ACID;

RARECHEM AL BO 0421.

 

Chemical & Physical Properties

Appearance:Colorless liquid

Assay: NLT99%

Melting Point:-15.4 °C (lit.)

Boiling point:72.4 °C (lit.)

Density:1.489 g/mL at 20 °C (lit.)

Solubility: Miscible with ethe r, ac etone, ethanol, benzene, hexane, and CCl<sub>4</sub>

 

Safety Information

Risk Statements: R20;R35;R52/53

Hazard Codes: C,T,Xi

HS Code: 2915900090

 

Application:Trifluoroacetic acid is mainly used in the production of new pesticides, medicines and dyes, and also has great application and development potential in materials, solvents and other fields.Trifluoroacetic acid is mainly used to synthesize a variety of herbicides containing trifluoromethyl and heterocyclic rings. Currently, it can synthesize a variety of new herbicides with pyridyl and quinolyl groups; as an extremely strong protonic acid, it is widely used in Catalyst for alkylation, acylation, olefin polymerization and other reactions of aromatic compounds; as a solvent, trifluoroacetic acid is an excellent solvent for fluorination, nitration and halogenation reactions, especially the effect of its derivative trifluoroacetyl on hydroxyl and amino groups Chemicalbook has excellent protective effects and has a very important application in the synthesis of amino acids and peptide compounds. It is used to remove the tert-butoxycarbonyl (t-boc) protecting group of amino acids in peptide synthesis; trifluoroacetic acid is used as a raw material and modification for the preparation of ion membranes. agent, which can greatly improve the current efficiency of caustic soda industry and extend the service life of membranes; trifluoroacetic acid can also synthesize trifluoroethanol, trifluoroacetaldehyde and trifluoroacetic anhydride.Mercury trifluoroacetate causes fluorobenzene to undergo a mercury reaction (electrophilic substitution) at room temperature, and can also convert hydrazones into diazo compounds.The lead salt of this acid converts aromatics into phenols.

 

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