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Trichloroacetyl chloride

CAS No.
76-02-8
Chemical Name:
Trichloroacetyl chloride
Synonyms
2,2,2-trichloroAcetyl chloride;CCl3COCl;Trichloroacetic chloride;Superpalite;TRICHLOROACETIC ACID CHLORIDE;Green cross gas;trichloroacetyl;Trichloroacetyl chlo;Trichloroacetochloride;trichloro-acetylchlorid
CBNumber:
CB6854254
Molecular Formula:
C2Cl4O
Molecular Weight:
181.83
MDL Number:
MFCD00000792
MOL File:
76-02-8.mol
MSDS File:
SDS
Last updated:2026-05-28 01:16:15
Product description Number Pack Size Price
Trichloroacetyl chloride 99% 151599 25G $43.8
Trichloroacetyl chloride 99% 151599 100G $119
Trichloroacetyl chloride 99% 151599 500G $321
Trichloroacetyl Chloride TRC-T773935-100G 100g $415
Trichloroacetyl chloride 99.0% 2116-4-03 1kg $295
More product size

Trichloroacetyl chloride Properties

Melting point -57 °C
Boiling point 114-116 °C(lit.)
Density 1.629 g/mL at 25 °C(lit.)
vapor pressure 16 mm Hg ( 20 °C)
refractive index n20/D 1.470(lit.)
Flash point 100 °C
storage temp. Refrigerator, Under inert atmosphere
solubility Chloroform (Soluble), Ethyl Acetate (Soluble)
form Oil
color Colourless
PH 1.11 (25°C, 16.2g/L in H2O)
Water Solubility reacts violently
Sensitive Moisture Sensitive
BRN 774120
Henry's Law Constant 2.0×10-2 mol/(m3Pa) at 25℃, Mirabel et al. (1996)
Stability Stable. Reacts violently with water. Incompatible with alcohols, oxidizing agents, strong bases.
InChI 1S/C2Cl4O/c3-1(7)2(4,5)6
InChIKey PVFOMCVHYWHZJE-UHFFFAOYSA-N
SMILES ClC(Cl)(Cl)C(=O)Cl
CAS DataBase Reference 76-02-8(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 9SN86T76Y6
NIST Chemistry Reference Trichloroacetyl chloride(76-02-8)
EPA Substance Registry System Trichloroacetyl chloride (76-02-8)
UNSPSC Code 12352106
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Skull and Crossbones (GHS06)
GHS05,GHS06
Signal word  Danger
Hazard statements  H330-H302-H314-H290
Precautionary statements  P501-P260-P270-P234-P271-P264-P280-P284-P390-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P403+P233-P406-P405
Hazard Codes  T+,T
Risk Statements  14-22-26-34-35-29
Safety Statements  26-28-36/37/39-45-8-28A-23
RIDADR  UN 2442
WGK Germany  3
RTECS  AO7140000
19
Hazard Note  Very Toxic
TSCA  TSCA listed
HazardClass  8
PackingGroup  II
HS Code  29159080
Storage Class 8A - Combustible, corrosive hazardous materials
Hazard Classifications Acute Tox. 4 Oral
Eye Dam. 1
Skin Corr. 1A
Hazardous Substances Data 76-02-8(Hazardous Substances Data)
REACH Registrations Inactive
Excepted Quantities Forbidden
NFPA 704
0
4 0
W

Trichloroacetyl chloride price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 151599 Trichloroacetyl chloride 99% 76-02-8 25G $43.8 2026-04-30 Buy
Sigma-Aldrich 151599 Trichloroacetyl chloride 99% 76-02-8 100G $119 2026-04-30 Buy
Sigma-Aldrich 151599 Trichloroacetyl chloride 99% 76-02-8 500G $321 2026-04-30 Buy
TRC TRC-T773935-100G Trichloroacetyl Chloride 76-02-8 100g $415 2026-06-03 Buy
SynQuest Laboratories 2116-4-03 Trichloroacetyl chloride 99.0% 76-02-8 1kg $295 2026-05-22 Buy
Product number Packaging Price Buy
151599 25G $43.8 Buy
151599 100G $119 Buy
151599 500G $321 Buy
TRC-T773935-100G 100g $415 Buy
2116-4-03 1kg $295 Buy

Trichloroacetyl chloride Chemical Properties,Uses,Production

Chemical Properties

Trichloroacetyl chloride is similar to dichloroacetyl chloride. It is a clear colourless liquid. Decomposes in water; soluble in alcohol.The acid chloride can be hydrolyzed at 75 – 85°C with water to form the free acid and hydrolyzed with ammonium hydroxide or concentrated sodium carbonate solution to form the salts.

Uses

Trichloroacetyl chloride can be used for the manufacture of the esters and the anhydrides of trichloroacetic acid.It was used in the preparation of dihydro-1H-benzindoles. It was also used in the synthesis of 3-alkylbenzoxazolones.

Uses

Trichloroacetyl Chloride is a reagent used to synthesize pyrazol-furan carboxamide analogues, which can act as Akt kinase inhibitors and pyrrolostatin, which can act as a lipid peroxidation inihibitor (1,2).

Preparation

The acetyl chloride is prepared from trichloroacetic acid and various inorganic acid chlorides (e.g., SOCl2, PCl3) or with P2O5 and HCl. More useful methods are the oxidation of tetrachloroethylene with fuming sulfuric acid, oxygen, or fuming nitric acid and sulfuric acid at 18-20°C, or from the reaction of pentachloroethane and dry oxygen under UV light. It has been obtained in 37 % yield from carbon tetrachloride and carbon monoxide in the presence of aluminum chloride at 200°C and high pressure.The most common production method is the gas-phase, photochemical oxidation of tetrachloroethylene with oxygen. The reaction is initiated with UV light, with radioactive irradiation, or it is sensitized with chlorine or iodine.

General Description

A colorless volatile liquid with a strong odor. Denser than water. Contact severely irritates skin, eyes and mucous membranes. May be very toxic by ingestion and inhalation. May be combustible.

Reactivity Profile

Trichloroacetyl chloride is incompatible with water, with strong oxidizing agents, alcohols, bases (including amines). May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

Health Hazard

Highly toxic by ingestion and inhalation; strong irritant to skin and tissues.

Fire Hazard

Material may burn but does not ignite readily. Poisonous if inhaled or swallowed; skin contact poisonous. Contact may cause burns to skin and eyes.

Potential Exposure

Used in chemical syntheses.

Shipping

UN2442 Trichloroacetyl chloride, Hazard class: 8; Labels: 8-Corrosive material, 6.1-Poisonous materials.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, ethers and metal salts. Violent reaction with water, forming hydrochloric acid and trichloroacetic acid.

Waste Disposal

Do not discharge into drains or sewers. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Controlled incineration (oxides of nitrogen are removed from the effluent gas by scrubbers and/or thermal devices) Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Global( 298)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co., Ltd
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View Lastest Price from Trichloroacetyl chloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Trichloroacetyl chloride pictures 2026-06-05 Trichloroacetyl chloride
76-02-8
25KG 98%min 30tons/month WUHAN FORTUNA CHEMICAL CO., LTD
2-Dimethylaminoethylami pictures 2026-05-28 2-Dimethylaminoethylami
76-02-8
$10.00 1KG 99% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
Trichloroacetyl chloride pictures 2026-03-20 Trichloroacetyl chloride
76-02-8
$10.00 1KG 99% 5tons Hebei Chuanghai Biotechnology Co., Ltd
Acetyl chloride, trichloro- Green cross gas Superpalite trichloroacetyl trichloro-acetylchlorid TRICHLOROACETYL CHLORIDE TRICHLOROACETIC ACID CHLORIDE Trichloroacetochloride Trichloroacethlchoride Trichloroacetyl chloride,97% Trichloroacetyl chloride ,98% Trichloroacetyl chlo Trichloro acetyl chloride (TCAC) Trichloroyxycnoic acid chloranehydride TrichIoroacetyl chIoride TRICHLOROACETYL CHLORIDE FOR SYNTHESIS 2-acetyl-2-chloro-2$l^{3}-trichloran-2-uide Trichloroacetyl chloride, 97% 250ML Acetyl chloride, 2,2,2-trichloro- TIANFU CHEM-- Trichloroacetyl chloride 2,2,2-trichloroAcetyl chloride CCl3COCl Trichloroacetic chloride 76-02-8 1976/2/8 76-02-6 1976-2-8 1976-02-8 C2CI4O Cl3CCOCl C2OCl4 Organic Building Blocks Acid Halides Acylation Building Blocks Carbonyl Compounds Pyridines Acid Halides Organics Acid HalidesDerivatization Reagents Carbonyl Compounds Derivatization Reagents GC Organic Building Blocks Reagents for Acylation