Butyl acrylateCAS NO.: 141-32-2 CAS NO.141-32-2

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Butyl acrylate
99.5% Butyl acrylate
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ProName: Butyl acrylateCAS NO.: 141-32-2
CasNo: 141-32-2
Molecular Formula: C7H12O2
Appearance: white powder
Application: Pharmaceutical intermediates
DeliveryTime: In stock
PackAge: bag
Port: China main port
ProductionCapacity: 10000 Kilogram/Day
Purity: 99%
Storage: Room temperature
Transportation: By Sea/Air/DHL
LimitNum: 1 Gram
Heavy metal: N/A
Grade: Industrial Grade
first class: 1-10

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Details

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.	flammables area
solubility	1.7g/l
form	liquid
color	clear colorless
odor	fruity
odor threshold	0.00055ppm
explosive limit	1.1-7.8%(v)
water solubility	1.4 g/l (20 ºc)
sensitive	light sensitive
merck	14,1539
brn	1749970
exposure limits	tlv-twa 10 ppm (～55 mg/m³) (acgih).
stability:	stable. flammable. incompatible with strong oxidizing agents, strong acids, strong bases.
inchikey	cqeyyjkewsmyfg-uhfffaoysa-n
cas database reference	141-32-2(cas database reference)
nist chemistry reference	2-propenoic acid, butyl ester(141-32-2)
epa substance registry system	butyl 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
f	10
autoignition temperature	559 °f
tsca	yes
hazardclass	3
packinggroup	iii
hs code	29161230
hazardous substances data	141-32-2(hazardous substances data)
toxicity	ld50 orally in rats: 3.73 g/kg (smyth)

msds information

provider	language
acros	english
sigmaaldrich	english
alfa	english

butyl acrylate usage and synthesis

chemical properties	butyl 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
uses	intermediate in organic synthesis, polymers and copolymers for solvent coatings, adhesives, paints, binders, emulsifiers.
uses	butyl 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
uses	n-butyl acrylate is used to make polymersthat are used as resins for textile and leatherfinishes, and in paints.
production methods	n-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 .
production methods	n-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.
definition	chebi: an acrylate ester obtained by the formal condensation of the hydroxy group of butan-1-ol with the carboxy group of acrylic acid.
general description	a 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 reactions	flammable. very slightly soluble in water.
reactivity profile	butyl 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].
hazard	moderate 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 hazard	vapor is irritating when breathed at high concentrations. contact with liquid causes irritation of skin and burning of eyes.
health hazard	n-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 hazard	highly 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.
potential exposure	butyl 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%.
carcinogenicity	not listed as a human carcinogen by acgih, california proposition 65, iarc, ntp, or osha.
metabolic pathway	after 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.
storage	butyl 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.
shipping	un2348 butyl acrylate, stabilized, hazard class: 3; labels: 3—flammable liquid.
purification methods	wash 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.]
incompatibilities	may 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 disposal	dissolve 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.