Crotonic acid

Crotonic acid Basic information
Product Name:Crotonic acid
Synonyms:’rotonicacid;2-Butensαure;3-methyl-acrylicaci;3-Methylacrylsαure;a-butenoicacid;Acrylic acid, 3-methyl-;CH3CH=CHCOOH;crotonic
CAS:3724-65-0
MF:C4H6O2
MW:86.09
EINECS:223-077-4
Product Categories:Pharmaceutical Intermediates;Fine Chemical
Mol File:3724-65-0.mol
Crotonic acid Structure
Crotonic acid Chemical Properties
Melting point 70-72 °C(lit.)
Boiling point 180-181 °C(lit.)
density 1.027 g/mL at 25 °C(lit.)
vapor density 2.97 (vs air)
vapor pressure 0.19 mm Hg ( 20 °C)
refractive index 1.4210 (estimate)
FEMA 3908 | (E)-2-BUTENOIC ACID
Fp 190 °F
pka4.80±0.10(Predicted)
Odorat 0.10 % in propylene glycol. roasted burnt
Odor Typemilky
Water Solubility soluble
LogP0.720
CAS DataBase Reference3724-65-0(CAS DataBase Reference)
NIST Chemistry ReferenceCrotonic acid(3724-65-0)
EPA Substance Registry SystemCrotonic acid (3724-65-0)
Safety Information
Hazard Codes C
Risk Statements 21/22-34
Safety Statements 26-36/37/39-45
RIDADR UN 2823 8/PG 3
WGK Germany 3
RTECS GQ2900000
Hazardous Substances Data3724-65-0(Hazardous Substances Data)
MSDS Information
ProviderLanguage
2-Butenoic acid English
SigmaAldrich English
ACROS English
ALFA English
Crotonic acid Usage And Synthesis
Chemical PropertiesCrotonic acid is a white or colorless, crystalline solid with a pungent odor. May be transported as a molten liquid.
UsesSynthesis of resins, polymers, plasticizers, drugs.
UsesCrotonic acid is used in the synthesis of resins, polymers, plasticizers, and drugs. It is also used as a softening agent for synthetic rubber and in medicinal chemicals.
DefinitionExists in cis and trans isomeric forms, the latter being the stable isomer used commercially. The cis form melts at 15C and is sometimes called isocrotonic acid.
General DescriptionA white crystalline solid. Shipped as either a solid or liquid. Melting point 59°F. Soluble in water and less dense than water. Flash point 190°F. Corrosive to metals and tissue.
Air & Water ReactionsSoluble in water.
Reactivity ProfileCrotonic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Crotonic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
HazardStrong irritant to tissue.
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.
Safety ProfilePoison by intraperitoneal route. Moderately toxic by ingestion, skin contact, and subcutaneous routes. A powerful corrosive and irritant. Flammable when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.
Potential ExposureUsed to make plastics, resins, plasticizers, lacquers, and medicines; other chemicals as a chemical intermediate.
ShippingUN2823 Crotonic acid, solid, Hazard class: 8; Labels: 8-Corrosive material.
IncompatibilitiesMay form explosive mixture with air. A strong reducing agent. The aqueous solution is a weak acid. Violent reaction with oxidizers, combustibles, strong bases; peroxides. Moisture or strong sunlight (UV) may cause explosive polymerization. May accumulate static electrical charges, and may cause ignition of its vapors. Combustible when exposed to heat or flame. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water, and a salt that may be harmful. Incompatible with arsenic compounds 938 Crotonic Acid (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, sulfides (releasing heat, toxic, and possibly flammable gases), thiosulfates, and dithionites (releasing hydrogen sulfate and oxides of sulfur).
Polybutene Ethyl 3,3-dimethylacrylate Methyl 3-aminocrotonate Maleic acid Tiglic aldehyde Maleic anhydride 2-Butene Crotonaldehyde Folic acid Isopropyl 3-aminocrotonate 2-Crotonic acid,ethyl ester,Crotonic acid ethyl Glycine Fumaric acid Crotonic acid 3-Amino-2-butenoic acid ethyl ester phosphoric acid Crotonic acid Crotonic acid methyl

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