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Benzoic acid, 4-heptyl-, 4-(2-methylbutyl)phenyl ester

Base Information
  • Chemical Name:Benzoic acid, 4-heptyl-, 4-(2-methylbutyl)phenyl ester
  • CAS No.:100545-68-4
  • Molecular Formula:C25H34 O2
  • Molecular Weight:366.5363
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50888794
  • Nikkaji Number:J1.550.286J
  • Mol file:100545-68-4.mol
Benzoic acid, 4-heptyl-, 4-(2-methylbutyl)phenyl ester

Synonyms:Benzoic acid, 4-heptyl-, 4-(2-methylbutyl)phenyl ester;100545-68-4;SCHEMBL20594581;DTXSID50888794;4-Heptylbenzoic acid 4-(2-methylbutyl)phenyl ester

Suppliers and Price of Benzoic acid, 4-heptyl-, 4-(2-methylbutyl)phenyl ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 21 raw suppliers
Chemical Property of Benzoic acid, 4-heptyl-, 4-(2-methylbutyl)phenyl ester
Chemical Property:
  • Vapor Pressure:2.14E-09mmHg at 25°C 
  • Boiling Point:480.6°Cat760mmHg 
  • Flash Point:203.5°C 
  • Density:0.988g/cm3 
  • XLogP3:9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:12
  • Exact Mass:366.255880323
  • Heavy Atom Count:27
  • Complexity:389
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)CC(C)CC
  • Use Description 4-(2-methylbutyl)phenyl 4-heptylbenzoate, also known as Isoamyl p-Methoxycinnamate, is a chemical compound with various applications in different fields. In the cosmetic and personal care industry, it is commonly used as an ingredient in sunscreens and skincare products due to its role as an effective UVB and UVA filter. Its ability to absorb and block harmful ultraviolet (UV) rays from the sun makes it valuable in protecting the skin from sunburn and UV-induced skin damage. Additionally, in the field of organic chemistry, it can serve as a reference compound for the study of cinnamate derivatives, contributing to our understanding of organic synthesis and structure-activity relationships. Its multifaceted applications highlight its significance in promoting skin protection and safety in cosmetics and its role in chemical research as a reference compound for structural analysis.
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