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Technology Process of Butyl prop-2-enoate;2-(dimethylamino)ethanol;2,2-dimethylpropane-1,3-diol;1,3-dioxo-2-benzofuran-5-carboxylic acid;hexanedioic acid;2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid

Butyl prop-2-enoate;2-(dimethylamino)ethanol;2,2-dimethylpropane-1,3-diol;1,3-dioxo-2-benzofuran-5-carboxylic acid;hexanedioic acid;2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid

Base Information
  • Chemical Name:Butyl prop-2-enoate;2-(dimethylamino)ethanol;2,2-dimethylpropane-1,3-diol;1,3-dioxo-2-benzofuran-5-carboxylic acid;hexanedioic acid;2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid
  • CAS No.:68583-86-8
  • Molecular Formula:C38H63NO19
  • Molecular Weight:837.9021
  • Hs Code.:
  • Mol file:68583-86-8.mol
Butyl prop-2-enoate;2-(dimethylamino)ethanol;2,2-dimethylpropane-1,3-diol;1,3-dioxo-2-benzofuran-5-carboxylic acid;hexanedioic acid;2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid

Synonyms:68583-86-8;(C9-H4-O5.C7-H12-O2.C6-H10-O4.C5-H12-O2.C4-H11-N-O.C4-H10-O3.C3-H4-O2)x-

Suppliers and Price of Butyl prop-2-enoate;2-(dimethylamino)ethanol;2,2-dimethylpropane-1,3-diol;1,3-dioxo-2-benzofuran-5-carboxylic acid;hexanedioic acid;2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of Butyl prop-2-enoate;2-(dimethylamino)ethanol;2,2-dimethylpropane-1,3-diol;1,3-dioxo-2-benzofuran-5-carboxylic acid;hexanedioic acid;2-(2-hydroxyethoxy)ethanol;prop-2-enoic acid
Chemical Property:
  • Boiling Point:470.6°Cat760mmHg 
  • Flash Point:201.3°C 
  • PSA：332.49000 
  • Density:g/cm3 
  • LogP:1.70920 
  • Hydrogen Bond Donor Count:9
  • Hydrogen Bond Acceptor Count:20
  • Rotatable Bond Count:20
  • Exact Mass:837.39942878
  • Heavy Atom Count:58
  • Complexity:674
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:UVCB
  • Canonical SMILES:CCCCOC(=O)C=C.CC(C)(CO)CO.CN(C)CCO.C=CC(=O)O.C1=CC2=C(C=C1C(=O)O)C(=O)OC2=O.C(CCC(=O)O)CC(=O)O.C(COCCO)O
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