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Henan Tianfu Chemical Co., Ltd.ALLYL ACRYLATE 999-55-3//file1.lookchem.com/cas/reactions/2021/06/09/1743576.png
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ALLYL ACRYLATE 999-55-3 CAS NO.999-55-3

Min.Order Quantity:
1 Kilogram
Purity:
99%
Port:
shanghai
Payment Terms:
T/T

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Product Details

Keywords

  • 2-Propenoic acid,2-propen-1-yl ester
  • 999-55-3
  • 98

Quick Details

  • ProName: ALLYL ACRYLATE 999-55-3
  • CasNo: 999-55-3
  • Molecular Formula: C6H8O2
  • Appearance: colorless liquid
  • Application: Organic Chemicals
  • DeliveryTime: within 1-2 week
  • PackAge: as requested
  • Port: shanghai
  • ProductionCapacity: 1 Metric Ton/Month
  • Purity: 99%
  • Storage: room temperature
  • Transportation: by sea
  • LimitNum: 1 Kilogram
  • Grade: Industrial Grade

Superiority

allyl acrylate basic information
product name: allyl acrylate
synonyms: acrylic acid allyl ester;allyl acrylate;2-propenoicacid,2-propenylester;2-propenyl ester of 2-propenoic acid;allylacrylate,stabilized,90+%;allyl acrylate, stabilized;allyl acrylate: tech., 85%;allyl acrylate 90+%, stab. with mehq
cas: 999-55-3
mf: c6h8o2
mw: 112.13
einecs: 213-662-2
product categories: monomer
mol file: 999-55-3.mol
allyl acrylate structure
allyl acrylate chemical properties
boiling point 46-47°c 40mm
density 0,935 g/cm3
refractive index 1.4360
fp 32°c
brn 1743576
stability: prone to polymerization. flammable. incompatible with strong oxidizing agents, acids, bases.
cas database reference 999-55-3(cas database reference)
safety information
risk statements 10-22-23/24-36/37/38
safety statements 25-36/37/39-45
ridadr 2929
rtecs ud3675000
hazardclass 6.1
packinggroup ii

Details

allyl acrylate usage and synthesis
chemical properties colourless liquid
general description clear colorless liquid.
air & water reactions slightly soluble in water.
reactivity profile the unsaturated aliphatic hydrocarbons, like allyl acrylate, are generally much more reactive than the alkanes, which are saturated aliphatic hydrocarbons. strong oxidizers may react vigorously with them. reducing agents can react exothermically to release gaseous hydrogen. in the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions. many of these compounds undergo autoxidation upon exposure to the air to form explosive peroxides. these peroxide and polyperoxide substances are usually extremely unstable and liable to detonation. the peroxidation of butadiene has been involved in several serious industrial accidents. esters react with acids to liberate heat along with alcohols and acids. strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. heat is also generated by the interaction of esters with caustic solutions. flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
fire hazard allyl acrylate is flammable.

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