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Homosalate information


Homosalate[1]
Skeletal formula
Space-filling model
Names
IUPAC name
3,3,5-Trimethylcyclohexyl 2-hydroxybenzoate
Other names
Homosalate
Identifiers
CAS Number
  • 118-56-9 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 8059 checkY
ECHA InfoCard 100.003.874 Edit this at Wikidata
KEGG
  • D04450 checkY
PubChem CID
  • 8362
UNII
  • V06SV4M95S checkY
CompTox Dashboard (EPA)
  • DTXSID1026241 Edit this at Wikidata
InChI
  • InChI=1S/C16H22O3/c1-11-8-12(10-16(2,3)9-11)19-15(18)13-6-4-5-7-14(13)17/h4-7,11-12,17H,8-10H2,1-3H3 checkY
    Key: WSSJONWNBBTCMG-UHFFFAOYSA-N checkY
  • InChI=1/C16H22O3/c1-11-8-12(10-16(2,3)9-11)19-15(18)13-6-4-5-7-14(13)17/h4-7,11-12,17H,8-10H2,1-3H3
    Key: WSSJONWNBBTCMG-UHFFFAOYAJ
SMILES
  • O=C(OC1CC(CC(C1)(C)C)C)c2ccccc2O
Properties
Chemical formula
C16H22O3
Molar mass 262.349 g·mol−1
Density 1.05 g/cm3 (20 °C)[2]
Melting point < -20 °C[2]
Boiling point 181–185 °C (358–365 °F; 454–458 K)[2]
Solubility in water
0.4 mg/L
Hazards
Flash point 171 °C (340 °F; 444 K)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Homosalate is an organic compound used in some sunscreens. It is made by the Fischer–Speier esterification of salicylic acid and 3,3,5-trimethylcyclohexanol, the latter being a hydrogenated derivative of isophorone. Contained in 45% of U.S. sunscreens, it is used as a chemical UV filter.[3] The salicylic acid portion of the molecule absorbs ultraviolet rays with a wavelength from 295 nm to 315 nm, protecting the skin from sun damage. The hydrophobic trimethyl cyclohexyl group provides greasiness that prevents it from dissolving in water.

  1. ^ Homosalate, Merck Index, 11th Edition, 4660.
  2. ^ a b c d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  3. ^ Homosalate, ChemIDplus.

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Homosalate

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Homosalate is an organic compound used in some sunscreens. It is made by the Fischer–Speier esterification of salicylic acid and 3,3,5-trimethylcyclohexanol...

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Sunscreen

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common petrochemical UV filters (avobenzone, oxybenzone, octocrylene, homosalate, octisalate, and octinoxate) found that they could be detected on the...

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UV filter

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classes: Benzophenones Benzophenone-3 (BP3) Benzophenone-4 (BP4) Salicylates Homosalate (HMS) 2-ethylhexyl salicylate (EHS) p-Aminobenzoic acid and derivatives...

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List of compounds with carbon number 16

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thonzylamine 91-85-0 C16H22O3 homomenthyl salicylate 52253-93-7 C16H22O3 homosalate 118-56-9 C16H22O3Si3 diphenyltetramethylcyclotrisiloxane 1693-51-2 C16H22O4...

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