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4-Methylbenzylidenecamphor

Base Information Edit
  • Chemical Name:4-Methylbenzylidenecamphor
  • CAS No.:38102-62-4
  • Deprecated CAS:38102-62-4,84055-65-2
  • Molecular Formula:C18H22O
  • Molecular Weight:254.36700
  • Hs Code.:2914399090
  • European Community (EC) Number:253-242-6
  • UNII:7576E1028E,8I3XWY40L9
  • DSSTox Substance ID:DTXSID70865901
  • Nikkaji Number:J2.174.049G
  • Wikipedia:Enzacamene
  • Wikidata:Q76393721
  • NCI Thesaurus Code:C87222
  • Mol file:38102-62-4.mol
4-Methylbenzylidenecamphor

Synonyms:3-(4'-methylbenzylidene)camphor;3-(4-methylbenzylidene)camphor;4-MBC cpd;4-methylbenzylidene camphor;enzacamene;Eusolex 6300;Eusolex-6300

Suppliers and Price of 4-Methylbenzylidenecamphor
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • 3-(4-Methylbenzylidene)camphor ≥98.0% (GC)
  • 250 g
  • $ 134.00
  • Sigma-Aldrich
  • 3-(4-Methylbenzylidene)camphor certified reference material, TraceCERT?
  • 50 mg
  • $ 90.50
Total 44 raw suppliers
Chemical Property of 4-Methylbenzylidenecamphor Edit
Chemical Property:
  • Boiling Point:371.9oC at 760mmHg 
  • Flash Point:168.9oC 
  • PSA:17.07000 
  • Density:1.064g/cm3 
  • LogP:4.40360 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:254.167065321
  • Heavy Atom Count:19
  • Complexity:423
Purity/Quality:

98%,99%, *data from raw suppliers

3-(4-Methylbenzylidene)camphor ≥98.0% (GC) *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=C(C=C1)C=C2C3CCC(C2=O)(C3(C)C)C
  • Isomeric SMILES:CC1=CC=C(C=C1)/C=C/2\[C@H]3CC[C@@](C2=O)(C3(C)C)C
  • Use Description 4-Methylbenzylidene camphor (4MBC) is a chemical compound with several applications across different fields. In the cosmetic and personal care industry, it is commonly used as a chemical UV filter in sunscreen and sunblock products, where it plays a crucial role in protecting the skin from the harmful effects of UV radiation by absorbing and dissipating UVB and UVA rays. In the field of materials science and polymer chemistry, it can be employed as an additive to enhance the UV stability and durability of various materials, including plastics, coatings, and textiles, which is important for outdoor applications that require UV resistance. Additionally, in research related to endocrine-disrupting chemicals (EDCs), 4MBC has been studied for its potential effects on hormone systems and aquatic life, raising concerns about its environmental impact when released into waterways. Its multifaceted roles as a UV filter, materials enhancer, and subject of environmental research highlight its significance in sun protection, materials development, and environmental awareness in various fields.
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