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avobenzone

Structure via PubChem · Public domain (PubChem)

EntityQ2775914· pop 15· linked from 56 articles

avobenzone

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Also known as Butyl Methoxydibenzoylmethane, Parsol 1789

Avobenzone (trade names Parsol 1789, Milestab 1789, Eusolex 9020, Escalol 517, Neo Heliopan 357 and others, INCI Butyl Methoxydibenzoylmethane) is an organic molecule and an oil-soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays.

Chemical data

Formula
C20H22O3
Molecular weight
310.4 g/mol
IUPAC name
1-(4-tert-butylphenyl)-3-(4-methoxyphenyl)propane-1,3-dione
SMILES
CC(C)(C)C1=CC=C(C=C1)C(=O)CC(=O)C2=CC=C(C=C2)OC
InChIKey
XNEFYCZVKIDDMS-UHFFFAOYSA-N
XLogP
4.8
Polar surface area
43.4 Ų
H-bond donors
0
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
1992
Admin. routes
topical
Indications
freckles, sunburn, skin cancer

via ChEMBL · EBI

Wikidata facts

Mass
310.157
Has use
sunscreen
Show 4 more facts
chemical formula
C₂₀H₂₂O₃
canonical SMILES
CC(C)(C)C1=CC=C(C=C1)C(=O)CC(=O)C2=CC=C(C=C2)OC
medical condition treated
photodermatitis
Commons category
Avobenzone
Sources (2)

via Wikidata · CC0

~7 min read

Encyclopedic overview

9 sections
Contents
  • History
  • Properties
  • Safety
  • Stability
  • Various
  • Absorbance spectrum
  • Preparation
  • See also
  • Notes

Avobenzone (trade names Parsol 1789, Milestab 1789, Eusolex 9020, Escalol 517, Neo Heliopan 357 and others, INCI Butyl Methoxydibenzoylmethane) is an organic molecule and an oil-soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays.

==History== Avobenzone was patented in 1973 and was approved in the EU in 1978. It was approved by the FDA in 1988. As of 2021, the FDA announced that they do not support avobenzone as being generally recognized as safe and effective (GRASE) citing the need for additional safety data. Avobenzone was banned in 2020 by the Palau government citing reef-toxicity concerns.

Excerpted from Wikipedia’s “avobenzone” article, available under the CC BY-SA 4.0 licence.

Gallery (9)