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Butyl acrylate

Butyl acrylate Suppliers list
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Products Intro: Product Name:Butyl acrylate
CAS:141-32-2
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CAS:141-32-2
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CAS:141-32-2
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CAS:141-32-2
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Products Intro: Product Name:Butyl acrylate
CAS:141-32-2
Purity:99% Package:180kg;15USD

Butyl acrylate manufacturers

  • Butyl acrylate
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  • 2023-12-25
  • CAS:141-32-2
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  • 2023-12-05
  • CAS:141-32-2
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  • Uses of Butyl acrylate
  • Butyl acrylate is a chemical intermediate manufactured and processed almost entirely within closed systems to produce homopoly....
  • Dec 1,2021
Butyl acrylate Basic information
Product Name:Butyl acrylate
Synonyms:n-Butyl acrylate, 98+%, stab. with up to 50ppM 4-Methoxyphenol;BUTYL ACRYLATE (STABILISED WITH HYDROQUI;BUTYL-2-ACRYLATE;Acrylsure-n-butylester;N-BUTYL ACRYLATE , STABILIZED WITH 50PPM 4-METHOXYPHENOL;Butyl acrylate;n-Butyl acrylate, 98+%, stab. with 50ppm 4-methoxyphenol;Butyl Acrylate (stabilized with MEHQ)
CAS:141-32-2
MF:C7H12O2
MW:128.17
EINECS:205-480-7
Product Categories:Acrylate;ester series;AcrylateCarbonyl Compounds;Acrylic Monomers;C6 to C7;Esters;Monomers;A-B;Alpha Sort;Volatiles/ Semivolatiles;Acrylic Monomers;Building Blocks;C6 to C7;Carbonyl Compounds;Chemical Synthesis;Materials Science;Organic Building Blocks;Polymer Science;Industrial/Fine Chemicals;141-32-2;K00001
Mol File:141-32-2.mol
Butyl acrylate Structure
Butyl acrylate Chemical Properties
Melting point -69 °C
Boiling point 61-63 °C60 mm Hg(lit.)
density 0.894 g/mL at 25 °C(lit.)
vapor density >1 (vs air)
vapor pressure 3.3 mm Hg ( 20 °C)
refractive index n20/D 1.410(lit.)
Fp 63 °F
storage temp. Store below +30°C.
solubility 1.7g/l
form Liquid
color Clear Colorless
OdorFruity
Odor Threshold0.00055ppm
explosive limit1.1-7.8%(V)
Water Solubility 1.4 g/L (20 ºC)
Sensitive Light Sensitive
Merck 14,1539
BRN 1749970
Exposure limitsTLV-TWA 10 ppm (~55 mg/m3) (ACGIH).
Stability:Stable. Flammable. Incompatible with strong oxidizing agents, strong acids, strong bases.
InChIKeyCQEYYJKEWSMYFG-UHFFFAOYSA-N
LogP2.38 at 25℃
CAS DataBase Reference141-32-2(CAS DataBase Reference)
IARC3 (Vol. 39, Sup 7, 71) 1999
NIST Chemistry Reference2-Propenoic acid, butyl ester(141-32-2)
EPA Substance Registry SystemButyl acrylate (141-32-2)
Safety Information
Hazard Codes F,Xn,Xi
Risk Statements 11-20/21/22-37/38-43-52/53-36/37/38-10
Safety Statements 16-25-37-61-9-36/37-26
RIDADR UN 1993 3/PG 2
WGK Germany 2
RTECS UD3150000
10
Autoignition Temperature559 °F
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29161230
Hazardous Substances Data141-32-2(Hazardous Substances Data)
ToxicityLD50 orally in rats: 3.73 g/kg (Smyth)
IDLA113 ppm
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Butyl acrylate Usage And Synthesis
DescriptionSensitization to n-butyl acrylate can occur in those in the dental profession.
Chemical PropertiesButyl acrylate is a colorless liquid with a sharp odor. It is readily miscible with most organic solvents. Butyl acrylate contains one of the following three inhibitors to prevent polymerization under recommended storage conditions:
Hydroquinone (HQ) CAS 123-31-95
Monomethyl ether of hydroquinone (MEHQ) CAS 150-76-5
Butylated hydroxytoluene (BHT) CAS 128-37-0
UsesIntermediate in organic synthesis, polymers and copolymers for solvent coatings, adhesives, paints, binders, emulsifiers.
Usesn-Butyl acrylate is used to make polymersthat are used as resins for textile and leatherfinishes, and in paints.
UsesButyl acrylate is primarily used as a reactive building block to produce coatings and inks,adhesives, sealants, textiles, plastics and elastomers. Butyl acrylate is used in the following applications:
Adhesives – for use in construction and pressure-sensitive adhesives
Chemical intermediates – for a variety of chemical products
Coatings – for textiles and adhesives, and for surface and water-based coatings, and coatings used for paints, leather finishing and paper
Leather – to produce different finishes, particularly nubuck and suede
Plastics – for the manufacture of a variety of plastics
Textiles – in the manufacture of both woven and non-woven textiles
Production Methodsn-Butyl acrylate can be manufactured via a reaction of acetylene, n-butyl alcohol, carbon monoxide, nickel carbonyl, and hydrochloric acid. It is commonly manufactured via an oxidation of propylene to acrolein and then to acrylic acid. The acid is reacted with n-butanol to yield the butyl ester .
DefinitionChEBI: An acrylate ester obtained by the formal condensation of the hydroxy group of butan-1-ol with the carboxy group of acrylic acid.
General DescriptionA clear colorless liquid with a sharp characteristic odor. Very slightly soluble in water and somewhat less dense than water. Hence forms surface slick on water. Flash point 105°F. Density 7.5 lb / gal. Used for making paints, coatings, caulks, sealants, adhesives.
Air & Water ReactionsFlammable. Very slightly soluble in water.
Reactivity ProfileButyl acrylate reacts exothermically with acids to liberate heat along with alcohols and acids. Reacts with strong oxidizing agents, perhaps sufficiently exothermically to ignite the reaction products. Mixing with basic solutions generates heat. Generates flammable hydrogen with alkali metals and hydrides. Attacks many plastics [Handling Chemicals Safely 1980. p. 233]. Polymerizes readily, generating much heat in a reaction that is favored by heat and light [Handling Chemicals Safely 1980. p. 235].
HazardModerate fire risk. Questionable carcinogen.
Acrylic esters, including butyl acrylate, have a very strong, unpleasant odor that may be bothersome. However, the smell of acrylates does not necessarily indicate a health risk. Acrylic esters have an extremely low odor “threshold,” meaning that even very small amounts in the air can be detected by smell.
Butyl acrylate liquid and vapors may cause slight eye irritation and even slight corneal damage. They may also cause pain greater than expected given the level of irritation.
Brief contact may cause moderate skin irritation with local redness. Prolonged contact may cause severe skin irritation with local redness and discomfort. Prolonged or widespread skin contact may result in absorption of harmful amounts and may cause an allergic skin reaction.
Excessive exposure to butyl acrylate vapors may cause irritation to upper respiratory tract (nose and throat) and lungs. Vapor concentrations are attainable which could be hazardous on single exposure.
Butyl acrylate has low toxicity if swallowed, but may result in gastrointestinal irritation or ulceration. Swallowing butyl acrylate may result in burns of the mouth and throat.
Butyl acrylate causes birth defects in laboratory animals only at doses toxic to the mother. It is toxic to the fetus in lab animals at doses toxic to the mother.
Health HazardVapor is irritating when breathed at high concentrations. Contact with liquid causes irritation of skin and burning of eyes.
Health Hazardn-Butyl acrylate is moderately irritating toskin. Its vapor is an irritant to mucous mem branes. The liquid caused corneal necrosiswhen instilled into rabbit eyes. The toxic andirritant properties of this compound are sim ilar to those of methyl acrylate. The adversehealth effects, however, are somewhat lessthan those of methyl and ethyl acrylates.The LD50 and LC50 values reported in theliterature show significant variations. Also,these data varied widely between mice andrats. The dermal LD50 value in rabbits is2000 mg/kg.
Fire HazardHIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. May polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Flammability and ExplosibilityFlammable
Potential ExposureButyl acrylate is a colorless liquid. Molecular weight 5 128.17; specific gravity (H2O:1) 5 0.89 @ 20C; boiling point 5 145148C; freezing/melting point 5 264.6C; vapor pressure 5 4 mmHg @ 20C; relative vapor density (air 5 1) 5 4.4; flash point 5 29C; vapor pressure 5 7.5 mmHg @ 30.4C; Autoignition temperature 5 292C. Explosive limits in air: LEL: 1.3%; UEL: 9.9%. Hazard identification (based on NFPA-704 M Rating System): Health 2; flammability 2; reactivity 2 ?. Slightly soluble in water; solubility in water = 0.14%.
First aidIf this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least30 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. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Medical observation is recommended for 24 48 h afterbreathing overexposure, as pulmonary edema may bedelayed. As first aid for pulmonary edema, a doctor orauthorized paramedic may consider administering a corticosteroid spray.
CarcinogenicityNot listed as a human carcinogen by ACGIH, California Proposition 65, IARC, NTP, or OSHA.
Metabolic pathwayAfter oral administration to rats, 14C-butyl acrylate is metabolized primarily to CO2, accounting for elimination of up to 75% of the radioactivity administered. Elimination in urine and feces accounts for approximately 10 and 2% of the dose, respectively. The major portion of butyl acrylate is hydrolyzed to acrylic acid, which is further metabolized to compounds available for oxidation. Two major metabolites identified in the urine are N-acetyl-S-(2- carboxyethyl)cysteine and its S-oxide. A smaller portion of butyl acrylate is conjugated with glutathione, and these conjugates result in the formation of the mercapturic acid excreted in the urine.
storageButyl acrylate is stable under recommended storage conditions. Elevated temperatures can cause hazardous polymerization. Polymerization can be initiated by the absence of air, the presence of free radical initiators and peroxides, or high temperature. The presence of moisture can also accelerate polymerization rate.
Butyl acrylate contains inhibitors to minimize polymerization under recommended storage conditions. Maintain inhibitor and dissolved oxygen level. Uninhibited monomer vapors can polymerize and plug relief devices.
Avoid unintended contact with activated carbon or silica gel, which may cause polymerization. Avoid contact with clay-based absorbants, and with incompatible materials, such as:
Oxidizing materials.
Aldehydes, amines, azides, ethers, free radical initiators, halides, mercaptans, mineral acids, peroxides, rust, strong inorganic bases.
Metals such as brass or copper.
ShippingUN2348 Butyl acrylate, stabilized, Hazard Class: 3; Labels: 3—Flammable liquid.
Purification MethodsWash it repeatedly with aqueous NaOH to remove inhibitors such as hydroquinone, then with distilled water. Dry with CaCl2. Fractionally distil under reduced pressure in an all-glass apparatus. The middle fraction is sealed under N2 and stored at 0o in the dark until required [Mallik & Das J Am Chem Soc 82 4269 1960]. [Beilstein 2 IV 1463.]
Toxicity evaluationButyl acrylate is a liquid (5 hPa at w20 °C) under normal environmental conditions. At equilibrium in the environment, butyl acrylate will partition primarily to air (95%) with the balance to water (5%). In air, butyl acrylate will be removed by reaction with photochemically produced hydroxyl radicals (28 h half-life) and ozone (6.5 days halflife). In water, butyl acrylate is relatively stable to hydrolysis at acidic and neutral pHs (half-life≥1100 days) but will slowly volatilize to air (Henry’s law constant of 21.9 Pa m-3 mol-1 at 25°C) or be biodegraded (58–90% removal in 28 days). Based on its relatively low octanol–water partition coefficient (log Kow of 2.38) and rapid metabolism in biological systems, butyl acrylate does not pose a significant bioaccumulation hazard.
IncompatibilitiesMay form explosive mixture with air. Heat, sparks, open flame, light, reducing agents; or peroxides may cause explosive polymerization. Incompatible with strong acids; amines, halogens, hydrogen compounds, oxidizers, sunlight, or other catalysts.
Waste DisposalDissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.
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