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2-Ethylhexyl salicylate

analytical standard

Synonym(s):

2-Ethylhexyl 2-hydroxybenzoate, Octisalate, Octyl salicylate

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About This Item

Linear Formula:
(HO)C6H4CO2CH2CH(C2H5)(CH2)3CH3
CAS Number:
Molecular Weight:
250.33
Beilstein:
2730664
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n/D 1.501-1.503
n20/D 1.502 (lit.)

bp

189-190 °C/21 mmHg (lit.)

density

1.014 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

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 is used as a UV filter in sunscreens.

Application

2-Ethylhexyl salicylate may be used as a reference standard for the determination of octyl salicylate as a UV filter authorized in sunscreens by high-performance liquid chromatography.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

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


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Development and Validation of RP-HPLC Method for Analysis of Four UV Filters in Sunscreen Products.
NAY, et al.
International Journal of Pharmaceutical Sciences Review and Research, 23(2), 254-258 (2013)
Determination of the UV filters worldwide authorised in sunscreens by high-performance liquid chromatography: use of cyclodextrins as mobile phase modifier.
Chisvert A, et al.
Journal of Chromatography A, 921(2), 207-215 (2001)
A DFT Investigation of the Molecular Structure and UV Absorption Spectra of 2-Ethylhexyl 2-Hydroxybenzoate (Octisalate) and Meta-Substituted 2-Ethylhexyl 2-Hydroxybenzoate: Sunscreen Applications
Punyain W.
Applied Mechanics and Materials, 855, 15-21 (2017)
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
K A Walters et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(12), 1219-1225 (1998-02-04)
The human skin penetration of [14C]octyl salicylate from two representative sunscreen vehicles was determined in vitro. 3H-sucrose was incorporated into all formulations and provided a marker for membrane integrity. When applied as a finite dose in an oil-in-water emulsion vehicle

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