Dichloroacetic acid CAS 79-43-6

Introduction:Basic information about Dichloroacetic acid CAS 79-43-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Dichloroacetic acid Basic information

Product Name:Dichloroacetic acid
Synonyms:DICHLOROACETICACID,REAGENT;DICHLOROACETIC ACID PESTANAL;DICHLOROACETIC ACID REAGENTPLUS(TM) &;DICHLOROACETIC ACID, 1000MG, NEAT;Dichloroaceticacid,99%;DICHLOROACETIC ACID REDISTILLED;Dichloressigsure;DCA Deblock (0.36M dichloroacetic acid in toluene)
CAS:79-43-6
MF:C2H2Cl2O2
MW:128.94
EINECS:201-207-0
Product Categories:Pharmaceutical Intermediates;Alpha Sort;D;DAlphabetic;DIA - DIC;Volatiles/ Semivolatiles;Chemical Synthesis;Organic Acids;Synthetic Reagents;Essential Chemicals;Pesticides&Metabolites;500 Series Drinking Water Methods;EPA;Method 552;Reagent Plus;Routine Reagents;intermediates
Mol File:79-43-6.mol

Dichloroacetic acid Chemical Properties

Melting point 9-11 °C(lit.)
Boiling point 194 °C(lit.)
density 1.56 g/mL at 25 °C (lit.)
vapor density 4.5 (vs air)
vapor pressure 0.19 mm Hg ( 20 °C)
refractive index n20/D 1.466(lit.)
Fp >230 °F
storage temp. Store below +30°C.
solubility Chloroform (Slightly), Methanol (Slightly)
pka1.48(at 25℃)
form Liquid
color APHA: <50
PH1.2 (129g/l, H2O, 20℃)
Water Solubility soluble
Sensitive Hygroscopic
Merck 14,3050
BRN 1098596
Dielectric constant10.7(-7℃)
Exposure limitsACGIH: TWA 0.5 ppm (Skin)
Stability:Stable. Incompatible with strong oxidizing agents, strong bases, strong reducing agents. Reacts with water. Protect from moisture. Hygroscopic.
InChI1S/C2H2Cl2O2/c3-1(4)2(5)6/h1H,(H,5,6)
InChIKeyJXTHNDFMNIQAHM-UHFFFAOYSA-N
SMILESOC(=O)C(Cl)Cl
LogP0.92
CAS DataBase Reference79-43-6(CAS DataBase Reference)
IARC2B (Vol. 63, 84, 106) 2014
NIST Chemistry ReferenceAcetic acid, dichloro-(79-43-6)
EPA Substance Registry SystemDichloroacetic acid (79-43-6)

Safety Information

Hazard Codes Xn,N,C,Xi,F
Risk Statements 36/38-40-50-35-36/37/38-67-38-65-48/20-11-63-50/53
Safety Statements 26-45-61-36/37-36-16-62-36/37/39
RIDADR UN 1764 8/PG 2
WGK Germany 2
RTECS AG6125000
3-10
TSCA TSCA listed
HS Code 2915 40 00
HazardClass 8
PackingGroup II
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Dermal
Aquatic Acute 1
Carc. 2
Eye Dam. 1
Lact.
Met. Corr. 1
Repr. 1B
Skin Corr. 1A
STOT RE 2 Oral
Hazardous Substances Data79-43-6(Hazardous Substances Data)
ToxicityLD50 orally in rats: 2.82 g/kg (Smyth)

Dichloroacetic acid Usage And Synthesis

DescriptionDCA is a corrosive, combustible, colorless liquid with a pungent odor. Molecular weight = 128.94;Specific gravity (H2O:1) = 1.56; Boiling point = 193.8℃;Freezing/Melting point = 9.7-13.5℃; Vaporpressure = 1 mmHg at 44℃; Flash point = 110℃. HazardIdentification (based on NFPA-704 M Rating System):Health 3, Flammability 1, Reactivity 1. Highly corrosive.Soluble in water.
Chemical PropertiesDichloroacetic acid, CHCI2COOH, also known as dichlorethanoic acid, is a corrosive, combustible, colorless, strong liquid acid with a pungent odor. It is soluble in water and alcohol. Dichloroacetic acid (Ka=5.14 × 10-2) is a stronger acid than chloroacetic acid. Most chemical reactions are similar to those of chloroacetic acid, although both chlorine atoms are susceptible to reaction. Dichloroacetic acid is much more stable to hydrolysis than chloroacetic acid. It is a reactive intermediate in organic synthesis. Dichloroacetic acid is prepared by the chlorination of acetic acid.
UsesDichloroacetic acid is used as an intermediate to make other chemicals such as its salts and esters. It is involved as a test reagent for fiber analysis and a disinfectant. It is used to inhibit mitochondrial PDK (pyruvate dehydrogenase kinase) and to shift cellular metabolism from glycolysis to glucose oxidation. Further, it is used in the treatment for post-ischemic recovery.
PreparationDichloroacetic acid was reported to be first synthesized in 1864 by the further chlorination of monochloroacetic acid with chlorine (Beilstein Online, 2002). The most common production method for dichloroacetic acid is the hydrolysis of dichloroacetyl chloride, which is produced by the oxidation of trichloroethylene.
ApplicationDichloroacetic acid (DCA) is a chlorinated acetic acid that has been reported to be a mouse liver carcinogen. The varying degrees of swelling of polyester in different concentrations of DCA solution has been analyzed by phase-contrast microscopy. The efficiency of titanium dioxide (TiO2) nanoparticles to catalyze the photodegradation of DCA has been investigated.
Dichloroacetic acid (DCA) can be used as:
A reactant in the synthesis of chloroketones by reacting with esters in the presence of LiHMDS via Claisen-type homologation reaction.
A structure-directing agent, solvent, or plastdopant for the preparation of different morphologies of polyaniline (PANI). Self-assembling nanostructured PANI may be formed due to the presence of strong hydrogen bonding between DCA and aniline/polyaniline.
DefinitionChEBI: Dichloroacetic acid is an organochlorine compound comprising acetic acid carrying two chloro substituents at the 2-position. It occurs in nature in seaweed, Asparagopsis taxiformis. It has a role as an astringent and a marine metabolite. It is a monocarboxylic acid and an organochlorine compound. It derives from an acetic acid. It is a conjugate acid of a dichloroacetate.
General DescriptionDichloroacetic acid appears as a colorless crystalline solid melting at 49°F. Corrosive to metals and tissue.
Air & Water ReactionsSoluble in water.
Reactivity ProfileDichloroacetic acid is probably hygroscopic. Dichloroacetic acid reacts with water or steam. Dichloroacetic acid is incompatible with strong oxidizing agents, strong bases and strong reducing agents.
Health HazardTOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
Fire HazardCombustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
Flammability and ExplosibilityNon flammable
reaction suitabilityreaction type: Acetylations
reagent type: Lewis acid
Safety ProfileModerately toxic by skin contact and ingestion. It is corrosive to the skin, eyes, and mucous membranes. Questionable carcinogen with experimental tumorigenic data. Will react with water or steam to produce toxic and corrosive fumes. When heated to decomposition it emits toxic fumes of Cl-. See also CHLORIDES.
Potential ExposureThis haloacetic acid can be a byproduct of drinking water disinfection and may increase the riskof cancer. This chemical is used as starting material for theproduction of glyoxylic; dialkyloxy acids; and sulfonamides. It is also used as a fungicide, a medication; anda chemical intermediate in pharmaceuticals
First aidIf this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. If victim is conscious, administer water ormilk. Do not induce vomiting. Medical observation isrecommended for 2448 h after breathing overexposure, aspulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.
storageColor Code—White: Corrosive or Contact Hazard;Store separately in a corrosion-resistant location. Prior toworking with DCA you should be trained on its proper handling and storage. Store in tightly closed containers in acool, well-ventilated area away from incompatible materialslisted above. Metal containers involving the transfer of thischemical should be grounded and bonded. Where possible,automatically pump liquid from drums or other storage containers to process containers. Drums must be equipped withself-closing valves, pressure vacuum bungs, and flamearresters. Use only nonsparking tools and equipment, especially when opening and closing containers of this chemical. Sources of ignition, such as smoking and open flames,are prohibited where this chemical is used, handled, orstored in a manner that could create a potential fire orexplosion hazard. Wherever this chemical is used, handled,manufactured, or stored, use explosion-proof electricalequipment and fittings.
ShippingUN1764 Dichloricacetic acid, Hazard class: 8;Labels: 8-Corrosive material.
Purification MethodsCrystallise this strong acid from *benzene or pet ether. Dry it with MgSO4 and fractionally distil it. [Bernasconi et al. J Am Chem Soc 107 3612 1985, Beilstein 2 IV 498.]
IncompatibilitiesDCA is a medium strong acid; incompatible with nonoxidizing mineral acids; organic acids; bases,acrylates, aldehydes, alcohols, alkylene oxides; ammonia,aliphatic amines; alkanolamines, aromatic amines; amides,furfuryl alcohol (explosion hazard), glycols, isocyanates,ketones. Attacks metals generating flammable hydrogengas. Attacks some plastics, rubber, and coatings
Toxics Screening LevelThe initial risk screening level (IRSL) for dichloroacetic acid (DCA) is 0.07 μg/m3 (annualaveraging time) based on the Michigan Department of Environmental Quality (MDEQ), AirQuality Division (AQD) Rule 336.1231. The initial threshold screening level (ITSL) is 0.5 μg/m3(annual averaging time) based on Rule 336.1232 (1) (e) and (2) (c).

Dichloroacetic acid Preparation Products And Raw materials

Raw materialsChloral
Preparation ProductsChloroacetic acid-->Glyoxylic acid-->Basic Yellow 24-->Dichloroacetyl chloride-->HEPTENOPHOS-->Dichloroacetic acid methyl ester-->Allantoin-->Hemin-->2-(DICHLOROMETHYL)BENZIMIDAZOLETHIOL-->Sodium dichloroacetate-->Acetic acid, 2,2-dichloro-, (tetrahydro-2-furanyl)methyl ester
Dichloro[η(5):η(1)-N-dimethyl(tetramethylcyclopentadienyl)silyl(tert-butyl)amido]titanium CAS 162763
DICHLOROBIS(PYRIDINE)PALLADIUM(II) CAS 14872-20-9
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