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Safety Information

437379

Sigma-Aldrich

2-Ethylhexyl salicylate

99%

Synonym(s):

Octisalate, Octyl salicylate

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About This Item

Linear Formula:
(HO)C6H4CO2CH2CH(C2H5)(CH2)3CH3
CAS Number:
118-60-5
Molecular Weight:
250.33
Beilstein:
2730664
EC Number:
204-263-4
MDL number:
MFCD00053300
UNSPSC Code:
12162002
PubChem Substance ID:
24867367
NACRES:
NA.23

Assay

99%

form

liquid

refractive index

n20/D 1.502 (lit.)

bp

189-190 °C/21 mmHg (lit.)

density

1.014 g/mL at 25 °C (lit.)

SMILES string

CCCCC(CC)COC(=O)c1ccccc1O

InChI

1S/C15H22O3/c1-3-5-8-12(4-2)11-18-15(17)13-9-6-7-10-14(13)16/h6-7,9-10,12,16H,3-5,8,11H2,1-2H3

InChI key

FMRHJJZUHUTGKE-UHFFFAOYSA-N

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General description

2-Ethylhexyl salicylate(EHS) is an organic ultraviolet(UV) absorber that can be used as a photostable ingredient in cosmetic formulations. It shows an absorption spectra in the range of 280-320 nm in the UV region.

Application

EHS is a salicylic ester which can be used as an UV filter in sunscreen based creams.

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Chronic 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

323.6 °F - closed cup

Flash Point(C)

162 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

437379-BULK:
437379-500ML:
437379-100ML:
437379-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR0350
MKCN6732
MKCG8481
MKCD4609
MKBW2673V

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Optical and electron paramagnetic resonance studies of the excited triplet states of UV-B absorbers: 2-ethylhexyl salicylate and homomenthyl salicylate.
Sugiyama K, et al.
Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society for Photobiology, 14(9), 1651-1659 (2015)
A pendant peptide endows a sunscreen with water-resistance.
Ellison AJ and Raines RT
Organic & Biomolecular Chemistry, 16(39), 7139-7142 (2018)
M McVean et al.
Molecular carcinogenesis, 24(3), 169-176 (1999-04-16)
Topical application of alpha-tocopherol (alphaTH), the most prominent naturally occurring form of vitamin E, inhibits ultraviolet (UV) B-induced photocarcinogenesis and DNA photodamage in C3H mice in vivo. In this study, we compared alphaTH with other vitamin E compounds and with
R Jiang et al.
Journal of pharmaceutical sciences, 86(7), 791-796 (1997-07-01)
This study provides an investigation of the availability of octyl salicylate (OS), a common sunscreen agent, from liquid paraffin and the effect of OS on skin permeability. A model membrane system to isolate the vehicle effect from membrane permeability has
M McVean et al.
Carcinogenesis, 18(8), 1617-1622 (1997-08-01)
Ultraviolet B (UVB, 290-320 nm) exposure results in a variety of cellular insults including induction of cyclobutane pyrimidine dimers in DNA. Accumulation of these lesions can lead to mutations in critical genes and contribute to the development of nonmelanoma skin
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