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Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester

CAS 87605-70-7C5H8O2MW 100.12

Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester (CAS 87605-70-7) — formula C5H8O2, molecular weight 100.12; category organic chemicals.

Product Overview

CAS Number87605-70-7
Molecular FormulaC5H8O2
Molecular Weight100.12
Melting Point-96.2 °F (NTP, 1992)
Boiling Point211.6 °F at 760 mmHg (NTP, 1992)
LogP1.3
ApplicationsUses: Ethyl acrylate is used in the manufacture of water-based latex paints and adhesives, textile and paper coatings, leather finish resins, and in the production of acrylic fibers., Used to make acrylic resins for fibers, adhesives, binders, surface coatings, textiles, paper, and leather, [ACGIH], Monomer for acrylic resins, The monomer in the manufacture of water emulsion paint vehicles, the production of emulsion-based polymers used in textile and paper coatings, leather finish resins and adhesives. Imparts flexibility to hard films., Reported uses, Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association) [Table#739], Ethyl acrylate is a major component of straight acrylic emulsion polymers used in latex paints, a major monomer used in straight acrylic emulsion for textile applications, including backcoatings, fabric finishes, pigment binders, dirt release agents, and thickeners. Used to make emulsion polymers for paper coating, as pulp additives in floor polishes and sealants, in shoe polishes, in base coatings and surface impregnation of leather in adhesives, sealants, caulking compound and binders., For more Uses (Complete) data for Ethyl acrylate (7 total), please visit the HSDB record page., Ethyl acrylate is used in the production of polymers including resins, plastics, rubber, and denture material (L1233)., Use Classification: Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Industry Uses: Wrinkle resisting agent, Monomers, Lubricating agent, Other, Solvent, Intermediate, Hardener, Flocculating agent, Thickening agent, Consumer Uses: Monomers, Not Known or Reasonably Ascertainable, Household Products: Cosmetics product ingredient: Ethyl acrylate, Also known as: ethyl propenoate, acrylic acid ethyl ester, Source: Ethyl acrylate is a manufactured chemical. It is a colorless liquid with a strong odor. Ethyl acrylate can be used as a plasticizer to increase flexibility and durability of products. It is used in some mascara and false eye lash products., Potential health impacts: People may be exposed to ethyl acrylate by absorption through the skin, by inhalation, or by ingestion. Ethyl acrylate is a skin irritant and a sensitizer. Studies of laboratory animals exposed to ethyl acrylate by ingestion found increased rates of stomach cancer, but studies of other routes of exposures (by inhalation and through the skin) did not find increased cancers. The International Agency for Research on Cancer (IARC) has classified this compound a possible human carcinogen. The U.S. Environmental Protection Agency (U.S. EPA) classifies this compound as a probable human carcinogen. California Proposition 65 lists ethyl acrylate as a carcinogen., Product count: 45, Information on 30 consumer products that contain Ethyl acrylate in the following categories is provided:, • Auto Products, • Home Maintenance, • Inside the Home, • Personal Care, Methods of Manufacturing: Reaction of nickel carbonyl and acetylene with ethyl alcohol in the presence of an acid, or esterification of acrylic acid with ethyl alcohol (modified Repp process), Prepd from ethylene chlorohydrin or acrylonitrile, ethanol, and sulfuric acid., Vinyl chloride reacts at 270 °C at > 6895 kPa (68 atm) with ethanol in the presence of a cobalt and palladium catalyst to give ethyl acrylate in 17% yield ... ., Ethylene cyanohydrin, ethyl alcohol and dilute sulfuric acid. Oxo reaction of acetylene, carbon monoxide, and ethyl alcohol in the presence of nickel or cobalt catalyst., In ... propylene oxidation process acrolein is first formed by the catalytic oxidation of propylene vapor at high temp in the presence of steam. The acrolein is then oxidized to acrylic acid. ... The acrylic acid is esterified with alcohol to the ... acrylic ester in a separate process., Acrylic ester monomers, IFRA Fragrance Standards: Ethyl acrylate, Ethyl propenoate, 2-Propenoic acid, ethyl ester, IFRA_STD_139.pdf, 40, IFRA 51st Amendment - Guidance for the use of IFRA Standards, Prohibition: This material should not be used as a fragrance ingredient, DERMAL SENSITIZATION, This material should not be used as a fragrance ingredient., Impurities: Water: 0.05% by wt (max), acrylic acid: 0.005% by wt (max), Formulations, Preparations: Water: 0.10% by wt, max, acidity, as acrylic acid: 0.009% by wt, Typical properties for commercial grade ethyl acrylate available in US are ... purity 99.0%, acidity (as acrylic acid), 0.0008%, water, 0.03%, inhibitors, 15 or 200 mg, kg (ppm) hydroquinone monomethyl ether or 1000 mg, kg (ppm) hydroquinone., 99.5% by wt (min) inhibited with 15-20 ppm hydroquinone, 99.5% by wt (min) inhibited with hydroquinone or monomethyl ether of hydroquinone, Grades: Technical (inhibited, usually with hydroquinone or its monomethyl ether), Pure uninhibited, Consumption Patterns: (All acrylate esters, of which n-butyl acetate is the largest volume): surface coatings 44%, sealants 18%, textiles 15%, plastics additives 9%, paper 5%, other 9% (2000), (All acrylic esters) 47% for surface coatings, 22% for textiles, 7% for paper, 7% for polishes, 3% for leather, 9% for acrylic fibers, 5% for misc applications (1969), (All acrylic acid esters) 46% as a monomer for emulsion polymers and solution polymers in latex paints, 26% as a monomer for emulsion polymers in textile applications, 6% as a comonomer for acrylic fibers, 6% as a monomer for emulsion polymers in polishes, 6% as a monomer for emulsion polymers in paper applications, 4% as a monomer for emulsion polymers used in base coatings and surface impregnation of natural leather, 6% in misc applications (1973), 45% for coatings, 16% for textiles & leather finishes, 9% for paper coatings, 8% for adhesives, 6% for polyacrylates, 5% for polishes, 5% for acrylic fibers, 6% other (1983 est), Acrylates and acr
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Ethyl acrylate is used in the manufacture of water-based latex paints and adhesives, textile and paper coatings, leather finish resins, and in the production of acrylic fibers., Used to make acrylic resins for fibers, adhesives, binders, surface coatings, textiles, paper, and leather, [ACGIH], Monomer for acrylic resins, The monomer in the manufacture of water emulsion paint vehicles, the production of emulsion-based polymers used in textile and paper coatings, leather finish resins and adhesives. Imparts flexibility to hard films., Reported uses, Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association) [Table#739], Ethyl acrylate is a major component of straight acrylic emulsion polymers used in latex paints, a major monomer used in straight acrylic emulsion for textile applications, including backcoatings, fabric finishes, pigment binders, dirt release agents, and thickeners. Used to make emulsion polymers for paper coating, as pulp additives in floor polishes and sealants, in shoe polishes, in base coatings and surface impregnation of leather in adhesives, sealants, caulking compound and binders., For more Uses (Complete) data for Ethyl acrylate (7 total), please visit the HSDB record page., Ethyl acrylate is used in the production of polymers including resins, plastics, rubber, and denture material (L1233)., Use Classification: Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Industry Uses: Wrinkle resisting agent, Monomers, Lubricating agent, Other, Solvent, Intermediate, Hardener, Flocculating agent, Thickening agent, Consumer Uses: Monomers, Not Known or Reasonably Ascertainable, Household Products: Cosmetics product ingredient: Ethyl acrylate, Also known as: ethyl propenoate, acrylic acid ethyl ester, Source: Ethyl acrylate is a manufactured chemical. It is a colorless liquid with a strong odor. Ethyl acrylate can be used as a plasticizer to increase flexibility and durability of products. It is used in some mascara and false eye lash products., Potential health impacts: People may be exposed to ethyl acrylate by absorption through the skin, by inhalation, or by ingestion. Ethyl acrylate is a skin irritant and a sensitizer. Studies of laboratory animals exposed to ethyl acrylate by ingestion found increased rates of stomach cancer, but studies of other routes of exposures (by inhalation and through the skin) did not find increased cancers. The International Agency for Research on Cancer (IARC) has classified this compound a possible human carcinogen. The U.S. Environmental Protection Agency (U.S. EPA) classifies this compound as a probable human carcinogen. California Proposition 65 lists ethyl acrylate as a carcinogen., Product count: 45, Information on 30 consumer products that contain Ethyl acrylate in the following categories is provided:, • Auto Products, • Home Maintenance, • Inside the Home, • Personal Care, Methods of Manufacturing: Reaction of nickel carbonyl and acetylene with ethyl alcohol in the presence of an acid, or esterification of acrylic acid with ethyl alcohol (modified Repp process), Prepd from ethylene chlorohydrin or acrylonitrile, ethanol, and sulfuric acid., Vinyl chloride reacts at 270 °C at > 6895 kPa (68 atm) with ethanol in the presence of a cobalt and palladium catalyst to give ethyl acrylate in 17% yield ... ., Ethylene cyanohydrin, ethyl alcohol and dilute sulfuric acid. Oxo reaction of acetylene, carbon monoxide, and ethyl alcohol in the presence of nickel or cobalt catalyst., In ... propylene oxidation process acrolein is first formed by the catalytic oxidation of propylene vapor at high temp in the presence of steam. The acrolein is then oxidized to acrylic acid. ... The acrylic acid is esterified with alcohol to the ... acrylic ester in a separate process., Acrylic ester monomers, IFRA Fragrance Standards: Ethyl acrylate, Ethyl propenoate, 2-Propenoic acid, ethyl ester, IFRA_STD_139.pdf, 40, IFRA 51st Amendment - Guidance for the use of IFRA Standards, Prohibition: This material should not be used as a fragrance ingredient, DERMAL SENSITIZATION, This material should not be used as a fragrance ingredient., Impurities: Water: 0.05% by wt (max), acrylic acid: 0.005% by wt (max), Formulations, Preparations: Water: 0.10% by wt, max, acidity, as acrylic acid: 0.009% by wt, Typical properties for commercial grade ethyl acrylate available in US are ... purity 99.0%, acidity (as acrylic acid), 0.0008%, water, 0.03%, inhibitors, 15 or 200 mg, kg (ppm) hydroquinone monomethyl ether or 1000 mg, kg (ppm) hydroquinone., 99.5% by wt (min) inhibited with 15-20 ppm hydroquinone, 99.5% by wt (min) inhibited with hydroquinone or monomethyl ether of hydroquinone, Grades: Technical (inhibited, usually with hydroquinone or its monomethyl ether), Pure uninhibited, Consumption Patterns: (All acrylate esters, of which n-butyl acetate is the largest volume): surface coatings 44%, sealants 18%, textiles 15%, plastics additives 9%, paper 5%, other 9% (2000), (All acrylic esters) 47% for surface coatings, 22% for textiles, 7% for paper, 7% for polishes, 3% for leather, 9% for acrylic fibers, 5% for misc applications (1969), (All acrylic acid esters) 46% as a monomer for emulsion polymers and solution polymers in latex paints, 26% as a monomer for emulsion polymers in textile applications, 6% as a comonomer for acrylic fibers, 6% as a monomer for emulsion polymers in polishes, 6% as a monomer for emulsion polymers in paper applications, 4% as a monomer for emulsion polymers used in base coatings and surface impregnation of natural leather, 6% in misc applications (1973), 45% for coatings, 16% for textiles & leather finishes, 9% for paper coatings, 8% for adhesives, 6% for polyacrylates, 5% for polishes, 5% for acrylic fibers, 6% other (1983 est), Acrylates and acr.

Technical Profile

What this product is

Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester is a carbon-based organic compound with CAS registry number 87605-70-7 and molecular formula C5H8O2 (molecular weight 100.12), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 87605-70-7

Its molecular formula C5H8O2 comprises 5 C, 8 H, 2 O atoms.

Also known as: Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester · 异氰脲酸双(丙烯酰氧乙基)酯

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester?

The CAS registry number of Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester is 87605-70-7.

What is the molecular formula and molecular weight of Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester?

Molecular formula C5H8O2, molecular weight 100.12.

What other names is Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester known by?

It is also registered under: Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester, 异氰脲酸双(丙烯酰氧乙基)酯.

What are the documented applications of Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester?

Recorded applications: Uses: Ethyl acrylate is used in the manufacture of water-based latex paints and adhesives, textile and paper coatings, leather finish resins, and in the production of acrylic fibers., Used to make acrylic resins for fibers, adhesives, binders, surface coatings, textiles, paper, and leather, [ACGIH], Monomer for acrylic resins, The monomer in the manufacture of water emulsion paint vehicles, the production of emulsion-based polymers used in textile and paper coatings, leather finish resins and adhesives. Imparts flexibility to hard films., Reported uses, Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association) [Table#739], Ethyl acrylate is a major component of straight acrylic emulsion polymers used in latex paints, a major monomer used in straight acrylic emulsion for textile applications, including backcoatings, fabric finishes, pigment binders, dirt release agents, and thickeners. Used to make emulsion polymers for paper coating, as pulp additives in floor polishes and sealants, in shoe polishes, in base coatings and surface impregnation of leather in adhesives, sealants, caulking compound and binders., For more Uses (Complete) data for Ethyl acrylate (7 total), please visit the HSDB record page., Ethyl acrylate is used in the production of polymers including resins, plastics, rubber, and denture material (L1233)., Use Classification: Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Flavoring Agents -> JECFA Flavorings Index, Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes, Industry Uses: Wrinkle resisting agent, Monomers, Lubricating agent, Other, Solvent, Intermediate, Hardener, Flocculating agent, Thickening agent, Consumer Uses: Monomers, Not Known or Reasonably Ascertainable, Household Products: Cosmetics product ingredient: Ethyl acrylate, Also known as: ethyl propenoate, acrylic acid ethyl ester, Source: Ethyl acrylate is a manufactured chemical. It is a colorless liquid with a strong odor. Ethyl acrylate can be used as a plasticizer to increase flexibility and durability of products. It is used in some mascara and false eye lash products., Potential health impacts: People may be exposed to ethyl acrylate by absorption through the skin, by inhalation, or by ingestion. Ethyl acrylate is a skin irritant and a sensitizer. Studies of laboratory animals exposed to ethyl acrylate by ingestion found increased rates of stomach cancer, but studies of other routes of exposures (by inhalation and through the skin) did not find increased cancers. The International Agency for Research on Cancer (IARC) has classified this compound a possible human carcinogen. The U.S. Environmental Protection Agency (U.S. EPA) classifies this compound as a probable human carcinogen. California Proposition 65 lists ethyl acrylate as a carcinogen., Product count: 45, Information on 30 consumer products that contain Ethyl acrylate in the following categories is provided:, • Auto Products, • Home Maintenance, • Inside the Home, • Personal Care, Methods of Manufacturing: Reaction of nickel carbonyl and acetylene with ethyl alcohol in the presence of an acid, or esterification of acrylic acid with ethyl alcohol (modified Repp process), Prepd from ethylene chlorohydrin or acrylonitrile, ethanol, and sulfuric acid., Vinyl chloride reacts at 270 °C at > 6895 kPa (68 atm) with ethanol in the presence of a cobalt and palladium catalyst to give ethyl acrylate in 17% yield ... ., Ethylene cyanohydrin, ethyl alcohol and dilute sulfuric acid. Oxo reaction of acetylene, carbon monoxide, and ethyl alcohol in the presence of nickel or cobalt catalyst., In ... propylene oxidation process acrolein is first formed by the catalytic oxidation of propylene vapor at high temp in the presence of steam. The acrolein is then oxidized to acrylic acid. ... The acrylic acid is esterified with alcohol to the ... acrylic ester in a separate process., Acrylic ester monomers, IFRA Fragrance Standards: Ethyl acrylate, Ethyl propenoate, 2-Propenoic acid, ethyl ester, IFRA_STD_139.pdf, 40, IFRA 51st Amendment - Guidance for the use of IFRA Standards, Prohibition: This material should not be used as a fragrance ingredient, DERMAL SENSITIZATION, This material should not be used as a fragrance ingredient., Impurities: Water: 0.05% by wt (max), acrylic acid: 0.005% by wt (max), Formulations, Preparations: Water: 0.10% by wt, max, acidity, as acrylic acid: 0.009% by wt, Typical properties for commercial grade ethyl acrylate available in US are ... purity 99.0%, acidity (as acrylic acid), 0.0008%, water, 0.03%, inhibitors, 15 or 200 mg, kg (ppm) hydroquinone monomethyl ether or 1000 mg, kg (ppm) hydroquinone., 99.5% by wt (min) inhibited with 15-20 ppm hydroquinone, 99.5% by wt (min) inhibited with hydroquinone or monomethyl ether of hydroquinone, Grades: Technical (inhibited, usually with hydroquinone or its monomethyl ether), Pure uninhibited, Consumption Patterns: (All acrylate esters, of which n-butyl acetate is the largest volume): surface coatings 44%, sealants 18%, textiles 15%, plastics additives 9%, paper 5%, other 9% (2000), (All acrylic esters) 47% for surface coatings, 22% for textiles, 7% for paper, 7% for polishes, 3% for leather, 9% for acrylic fibers, 5% for misc applications (1969), (All acrylic acid esters) 46% as a monomer for emulsion polymers and solution polymers in latex paints, 26% as a monomer for emulsion polymers in textile applications, 6% as a comonomer for acrylic fibers, 6% as a monomer for emulsion polymers in polishes, 6% as a monomer for emulsion polymers in paper applications, 4% as a monomer for emulsion polymers used in base coatings and surface impregnation of natural leather, 6% in misc applications (1973), 45% for coatings, 16% for textiles & leather finishes, 9% for paper coatings, 8% for adhesives, 6% for polyacrylates, 5% for polishes, 5% for acrylic fibers, 6% other (1983 est), Acrylates and acr.

Which category does Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for Bis(acryloxyethyl) isocyanurate 2-propenoic acid, [dihydro-5-(2-hydroxyethyl)2,4,6-trioxo-1-triazine-1,3(2h,4h)-diyl]di-2,1-ethanediyl ester (CAS 87605-70-7), compiled from public chemistry databases.

Registry identifiers across databases

CAS 号87605-70-7
PubChem CID8821
分子式C5H8O2
IUPAC 名称ethyl prop-2-enoate
UNII(FDA)71E6178C9T
FEMA 编号2418
JECFA 编号1351

Computed descriptors

Molecular Weight100.12
XLogP31.3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass100.052429494
Monoisotopic Mass100.052429494
Topological Polar Surface Area26.3
Heavy Atom Count7

Physicochemical values on record

Boiling Point211.6 °F at 760 mmHg (NTP, 1992)
Boiling Point99.4 °C
Boiling Point99.00 to 100.00 °C. @ 760.00 mm Hg
Boiling Point99 °C
Boiling Point99-101 °C
Boiling Point211 °F
Boiling Point99.4 °C @760 [mm Hg]
Melting Point-96.2 °F (NTP, 1992)
Melting Point-71.2 °C
Melting Point-71 °C

Synonyms and trade names

ETHYL ACRYLATE; 140-88-5; Acrylic acid ethyl ester; Ethyl propenoate; 2-Propenoic acid, ethyl ester; Ethyl 2-propenoate; Ethylacrylaat; Ethylakrylat; Etil acrilato; Acrylic acid, ethyl ester; Aethylacrylat; Etilacrilatului; Akrylanem etylu; Carboset 511; Ethoxycarbonylethylene; Ethyl acrylate, inhibited

Regulatory listings held on file

法规与食品接触EU Flavoring substances
FDA Substance added to food: FLAVORING AGENT OR ADJUVANT
FDA Cumulative Estimated Daily Intake (CEDI): FCS
FDA 21 CFR 中列出的食品接触物质清单:FCS
Flavoring Agents
FLAVOURING_AGENT: Flavouring Agent
GHS 通报统计0.1% (2 / 4896)

GHS hazard classification

GHS 通报统计0.1% (2 / 4896)
已通报的危害声明H225, H302, H312, H315, H317, H319, H331, H335

What the public record says

异氰脲酸双(丙烯酰氧乙基)酯 · CAS 87605-70-7 · C5H8O2. UNII 71E6178C9T. Boiling Point: 211.6 °F at 760 mmHg (NTP, 1992); Boiling Point: 99.4 °C; Boiling Point: 99.00 to 100.00 °C. @ 760.00 mm Hg.

Source: PubChem / Wikidata; the batch COA governs where values differ.

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