Ethylhexyl Salicylate is being used in a wide range of cosmetic products to provide an appropriate Sun Protection Factor (SPF) in sunscreens or to protect cosmetics against UV radiation.
Ethylhexyl Salicylate is approved for the use in sun care preparations in many countries worldwide.
Ethylhexyl Salicylate is used Cosmetics and Sunscreens.
CAS Number: 118-60-5
EC Number: 204-263-4
MDL Number: MFCD00053300
UV-B absorber: oil soluble
Molecular Weight: 250.37 g/mol
INCI name: Ethylhexyl Salicylate
USAN: Octisalate
Chemical names: 2-Ethylhexyl salicylate
Empirical Formula: C15H22O3
SYNONYMS:
2-Ethylhexyl o-Hydroxybenzoate, Dermoblock OS, Escalol 587, Eusolex OS, HallBrite OS-USP, Neo Heliopan OS, Octyl Salicylate, Parsol EHS, 2-Ethylhexyl 2-hydroxybenzoate, 2-Ethylhexyl Ester Salicylic Acid, Solarom OS, Sunarome O, Sunarome WMO, 2-Ethylhexyl Salicylate, 2-ethylhexyl 2-hydroxybenzoate,
octisalate, 2-ethylhexyl salicylate, ethyl hexyl salicylate, 2-ethylhexyl ester salicylic acid, salicylic acid, 2-ethylhexyl ester, benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, 2-ethylhexyl ester benzoic acid, 2-hydroxy-, 2-hydroxy- 2-ethylhexyl ester benzoic acid, Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, Salicylic acid, 2-ethylhexyl ester, Sunarome O, Sunarome WMO, USAF DO-11, WMO, Dermoblock OS, Escalol 587, Ethylhexyl salicylate, Neo Heliopan OS, Octyl salicylate, Uvinul O-18, 2-Ethylhexyl 2-hydroxybenzoate, NSC 46151, Octisalate, 194304-34-2, 8014-40-2, 2-hydroxy-benzoicaci2-ethylhexylester,Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester,Benzoicacid,2-hydroxy-,2-ethylhexylester,Dermoblock OS,Escalol 587,Ethylhexyl salicylate,Neo Heliopan OS,piedmonti,2-ethvlhexvlsavlate, Octyl salicylate, Ethylhexyl salicylate, 2-Ethylhexyl salicylate, 2-Ethylhexyl 2-hydroxybenzoate, 194304-34-2, 2-hydroxy-benzoicaci2-ethylhexylester, 8014-40-2, Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, Benzoicacid,2-hydroxy-,2-ethylhexylester, Dermoblock OS, Escalol 587, Neo Heliopan OS, NSC 46151, Octisalate, piedmonti,2-ethvlhexvlsavlate, Salicylic acid, 2-ethylhexyl ester, Salicylic acid-2-ethylhexyl ester, Sunarome O, Sunarome WMO, USAF DO-11, Uvinul O-18, WMO, 2-Ethylhexyl o-Hydroxybenzoate, Dermoblock OS, Escalol 587, Eusolex OS, HallBrite OS-USP, Neo Heliopan OS, Octyl Salicylate, Parsol EHS, 2-Ethylhexyl 2-hydroxybenzoate, 2-Ethylhexyl Ester Salicylic Acid, Solarom OS, Sunarome O, Sunarome WMO, Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, 2-Ethylhexyl salicylate (USP), 2-ETHYLHEXYL SALICYLATE, Octisalate, 118-60-5, 2-Ethylhexyl 2-hydroxybenzoate, Ethylhexyl salicylate, Ethyl hexyl salicylate, Sunarome O, Sunarome WMO, Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, Uvinul, Escalol, USAF DO-11, Neo Heliopan, Salicylic acid, 2-ethylhexyl ester, NSC 46151, Salicylic Acid 2-Ethylhexyl Ester, NSC-46151, WMO, DTXSID7040734, CHEBI:88639, MFCD00053300, 4X49Y0596W, NCGC00159324-02, Octyl salicylate, 2-Ethylhexyl salicylate, Octisalate [USAN], DTXCID5020734, CAS-118-60-5, EINECS 204-263-4, BRN 2730664, Octisalate [USAN:USP], Dermoblock OS, UNII-4X49Y0596W, Neo Heliopan OS, Uvinul (TN), Escalol 587, Salicylic acid-2-ethyl-1-hexyl ester, Uvinul O-18, 2-Hydroxybenzoic acid 2-ethylhexyl ester, OCTISALATE [II], Octisalate (USP/INN), Ethylhexyl salicylic acid, OCTISALATE [INN], OCTISALATE [VANDF], Salicylic Acid Octyl Ester, EC 204-263-4, OCTISALATE [MART.], OCTISALATE [USP-RS], OCTISALATE [WHO-DD], SCHEMBL39594, 2-Ethylhexyl2-hydroxybenzoate, OCTYL SALICYLATE [MI], 2-Ethylhexyl salicylate, 99%, CHEMBL1329203, OCTYL SALICYLATE [VANDF], WLN: QR BVO1Y4 & 2, 2-Ethylhexyl salicylate, >=99%, OCTISALATE [USP MONOGRAPH], HY-B0929, NSC46151, Tox21_111573, ETHYLHEXYL SALICYLATE [VANDF], s6405, STL570066, AKOS015890505, Tox21_111573_1, 1ST3405, CS-4398, DB11062, NCGC00159324-03, NCGC00159324-04, AC-12458, LS-14437, SY052290, 2-hydroxy benzoic acid 2-ethylhexyl ester, DB-041415, 2-Ethylhexyl salicylate, analytical standard, NS00011474, S0387, D05226, F85195, EN300-7381990, A804061, J-509330, Q27160526, Octisalate, United States Pharmacopeia (USP) Reference Standard, Octisalate, Pharmaceutical Secondary Standard; Certified Reference Material, Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, Salicylic acid, 2-ethylhexyl ester, Sunarome O, Sunarome WMO, USAF DO-11, WMO, Dermoblock OS, Escalol 587, Ethylhexyl salicylate, Neo Heliopan OS, Octyl salicylate, Uvinul O-18, 2-Ethylhexyl 2-hydroxybenzoate, NSC 46151, Octisalate, 194304-34-2, 8014-40-2, Salicylic Acid 2-Ethylhexyl Ester, Octyl Salicylate, Salicylic Acid Octyl Ester, octisalate, 2-ethylhexyl salicylate, ethyl hexyl salicylate, 2-ethylhexyl ester salicylic acid, salicylic acid, 2-ethylhexyl ester, benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, 2-ethylhexyl ester benzoic acid, 2-hydroxy-, 2-hydroxy- 2-ethylhexyl ester benzoic acid, 2-ethylhexyl 2-hydroxybenzoate, 2-ETHYLHEXYL SALICYLATE, Octisalate, 118-60-5, 2-Ethylhexyl 2-hydroxybenzoate, Ethylhexyl salicylate, Ethyl hexyl salicylate, Sunarome O, Sunarome WMO, Benzoic acid, 2-hydroxy-, 2-ethylhexyl ester, Uvinul, Escalol, USAF DO-11, Neo Heliopan, Salicylic acid, 2-ethylhexyl ester, NSC 46151, Salicylic Acid 2-Ethylhexyl Ester, MFCD00053300, NSC-46151, WMO, DTXSID7040734, CHEBI:88639, 4X49Y0596W, NCGC00159324-02, Octyl salicylate, 2-Ethylhexyl salicylate, Octisalate [USAN], DTXCID5020734, CAS-118-60-5, EINECS 204-263-4, BRN 2730664, Octisalate [USAN:USP:INN], Dermoblock OS, UNII-4X49Y0596W, Neo Heliopan OS, Uvinul (TN), Escalol 587, Salicylic acid-2-ethyl-1-hexyl ester, Uvinul O-18, Octisalate (Standard), 2-Hydroxybenzoic acid 2-ethylhexyl ester, OCTISALATE [II], Octisalate (USP/INN), Ethylhexyl salicylic acid, OCTISALATE [INN], OCTISALATE [VANDF], Salicylic Acid Octyl Ester, EC 204-263-4, OCTISALATE [MART.], OCTISALATE [USP-RS], OCTISALATE [WHO-DD], SCHEMBL39594, 2-Ethylhexyl2-hydroxybenzoate, OCTYL SALICYLATE [MI], 2-Ethylhexyl salicylate, 99%, CHEMBL1329203, OCTYL SALICYLATE [VANDF], HY-B0929R, WLN: QR BVO1Y4 & 2, 2-Ethylhexyl salicylate, >=99%, OCTISALATE [USP MONOGRAPH], HY-B0929, NSC46151, Tox21_111573, ETHYLHEXYL SALICYLATE [VANDF], s6405, STL570066, AKOS015890505, Tox21_111573_1, 1ST3405, CS-4398, DB11062, NCGC00159324-03, NCGC00159324-04, AC-12458, LS-14437, SY052290, 2-hydroxy benzoic acid 2-ethylhexyl ester, DB-041415, 2-Ethylhexyl salicylate, analytical standard, NS00011474, S0387, D05226, F85195, EN300-7381990, J-509330, Q27160526, Octisalate, United States Pharmacopeia (USP) Reference Standard, Octisalate, Pharmaceutical Secondary Standard, Certified Reference Material,
Ethylhexyl salicylate is a synthetic sunscreen ingredient that works primarily in the range of UVB light, although it offers a small amount of UVA protection.
Ethylhexyl Salicylate is also known as octyl salicylate and octisalate.
Research has shown this UV filter can neutralize singlet oxygen, a type of skin-damaging free radical generated by exposure to UVB light.
Ethylhexyl salicylate is described as a colorless liquid in raw material form.
Ethylhexyl salicylate has been deemed safe as used in cosmetics (by the Personal Care Council Cosmetic Ingredient Review Expert Panel) and is not considered an eye or skin irritant.
This salicylic acid derivative (Ethylhexyl Salicylate) is a sun protection filter that helps absorb UV rays.
Ethylhexyl Salicylate, also called octyl salicylate is an organic compound that works as a blocking agent for ultraviolet (UV) rays, particularly, UVB rays.
Ethylhexyl Salicylate is found in sunscreens and other cosmetic products and is a clear to light-yellow oily liquid.
Ethylhexyl salicylate, also known as octisalate on sunscreen product labels, is an ester of salicylic acid that may be used in cosmetics, personal care products and sunscreen products.
Ethylhexyl Salicylate is a colorless, crystalline organic acid that can be derived from salicin, a β-glucoside in willow tree bark.
While Ethylhexyl Salicylate is chemically similar to aspirin (acetylsalicylic acid), it is not identical.
Ethylhexyl Salicylate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
Ethylhexyl salicylate is a benzoate ester and a member of phenols.
Ethylhexyl Salicylate is functionally related to a salicylic acid.
Ethylhexyl Salicylate has been reported in Camellia sinensis, Homo sapiens, and Lonicera japonica with data available.
Ethylhexyl Salicylate is a small molecule drug with a maximum clinical trial phase of II.
Ethylhexyl Salicylate is the ester of 2-ethylhexyl alcohol and salicylic acid.
Ethylhexyl Salicylate is also approved as a sunscreen active ingredient in Canada, Japan, Australia and the European Union.
Ethylhexyl Salicylate is a weak UVB absorber with a generally good safety profile among sunscreen ingredients.
Ethylhexyl Salicylate is a penetration enhancer, which may increase the amount of other ingredients passing through skin
Ethylhexyl Salicylate, colorless or yellowish liquid, slightly soluble in water, soluble in alcohols and oils.
Ethylhexyl Salicylate is used in cosmetics as an organic filter, a photoprotective additive in UVB tanning products.
Ethylhexyl Salicylate is found in some plants, such as birch bark.
Ethylhexyl Salicylate is permitted as a UV filter under EU Regulation 1223/2009 and CU TR 009/2011 in concentrations not exceeding 5%.
Ethylhexyl Salicylate is a sunscreen ingredient with a generally good safety profile.
Ethylhexyl Salicylate, or 2-ethylhexyl salicylate, also called octyl salicylate is an organic compound that works as a blocking agent for ultraviolet (UV) rays, particularly, UVB rays.
Ethylhexyl Salicylate is found in sunscreens and other cosmetic products and is a clear to light-yellow oily liquid.
Ethylhexyl Salicylate is a colorless to light yellowish oily liquid that works as a UVB (280-320nm) sunscreen filter with a peak absorbance at 306 nm.
Ethylhexyl Salicylate has a good safety profile and is allowed to be used at a max concentration of 5% both in the US and in Europe (10% is allowed in Japan).
Ethylhexyl Salicylate also known as octisalate or octyl salicylate, is an organic compound used as an ingredient in sunscreens and cosmetics to absorb UVB (ultraviolet) rays from the sun.
Ethylhexyl Salicylate is an ester formed by the condensation of salicylic acid with 2-ethylhexanol.
Ethylhexyl Salicylate is a colorless oily liquid with a slight floral odor.
The salicylate portion of the molecule absorbs ultraviolet light, protecting skin from the harmful effects of exposure to sunlight.
The ethylhexanol portion is a fatty alcohol, adding emollient and oil-like (water resistant) properties.
Ethylhexyl Salicylate is a very effective UV-B absorber and has a wide use in sunscreen and skin care products to give UV-B radiation protection.
USES and APPLICATIONS of ETHYLHEXYL SALICYLATE:
Ethylhexyl Salicylate acts as a UV-B sunscreen agent.
Ethylhexyl Salicylate protects skin from harmful UV radiation and increase the effectiveness of sunscreen and daily wear formulations.
Ethylhexyl Salicylate is recommended for use in color cosmetics and hair-, skin-, baby- & nail care products.
Ethylhexyl Salicylate is also known under the names Octyl salicylate, Octisalate or 2-ethylhexyl salicylate.
EHS is better known as Ethylhexyl Salicylate.
Ethylhexyl Salicylate is an organic, oil-soluble sun filter that absorbs UV-B radiation.
Ethylhexyl Salicylate is an ester of salicylic acid and 2-ethylhexanol.
The salicylate portion of the molecule absorbs UV light to protect skin from the harmful effects of exposure to sunlight.
The ethylhexanol portion functions as an emollient.
Ethylhexyl Salicylate is a colorless liquid with an oily consistency that often emits a mildly floral fragrance.
Salicylates are weak UV-B absorbers.
They are often used in combination with other UV filters like AakoSun OMC.
This globally used sunscreen ingredient, Ethylhexyl Salicylate, is approved in varying concentrations around the world, with 5% being the typical maximum amount when combined with other UV filters.
Combining ethylhexyl salicylate with other UV filters is necessary since it doesn’t provide sufficient broad-spectrum protection on its own.
Ethylhexyl Salicylate is known to improve the stability of other UV filters like oxybenzone and avobenzone.
Ethylhexyl Salicylate is used by consumers, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Ethylhexyl Salicylate is used in the following products: cosmetics and personal care products and perfumes and fragrances.
Other release to the environment of Ethylhexyl Salicylate is likely to occur from: indoor use as processing aid and outdoor use as processing aid.
Ethylhexyl Salicylate is used in the following products: cosmetics and personal care products.
Ethylhexyl Salicylate is used for the manufacture of: chemicals and furniture.
Other release to the environment of Ethylhexyl Salicylate is likely to occur from: indoor use as processing aid and outdoor use as processing aid.
Ethylhexyl Salicylate is used in the following products: cosmetics and personal care products, perfumes and fragrances and welding & soldering products.
Release to the environment of Ethylhexyl Salicylate can occur from industrial use: formulation of mixtures.
Ethylhexyl Salicylate is used in the following products: cosmetics and personal care products.
Ethylhexyl Salicylate is used for the manufacture of: chemicals.
Release to the environment of Ethylhexyl Salicylate can occur from industrial use: in processing aids at industrial sites.
Release to the environment of Ethylhexyl Salicylate can occur from industrial use: manufacturing of the substance.
Ethylhexyl Salicylate is an oil soluble chemical sunscreen agent that absorbs UVB radiation.
Ethylhexyl Salicylate does not protect against UVA.
Ethylhexyl Salicylate is used to augment the UVB protection in a sunscreen.
Salicylates are weak UVB absorbers and they are generally used in combination with other UV filters.
Ethylhexyl Salicylate appears to have a good safety profile.
Ethylhexyl Salicylate covers wavelength in the range 295-315 nm, peak at 307-310 nm.
Ethylhexyl Salicylate is an ester of salicylic acid and 2-ethylhexanol.
The salicylate portion of the molecule absorbs ultraviolet light to protect skin from the harmful effects of exposure to sunlight, while the ethylhexanol portion functions as an emollient.
Ethylhexyl Salicylate is used as a sunscreen active ingredient in over-the-counter (OTC) sunscreens products that are applied to the skin to absorb, reflect or scatter UV rays.
Exposing unprotected skin to UV light can result in sunburn (primarily from UVB rays) and accelerate premature skin aging, as well as skin cancer (primarily from UVA rays).
Because ethylhexyl salicylate absorbs and dissipates UV radiation, it can protect cosmetics and personal care products from deterioration due to exposure to UV light and is used as a fragrance ingredient.
Ethylhexyl Salicylate's not a strong filter in itself, it's always used in combination with other sunscreen agents to further enhance the SPF and to solubilize other solid UV filters.
Ethylhexyl Salicylate is not a strong UV filter and is used in combination with other sunscreen agents.
Other benefits of Ethylhexyl Salicylate include being used for low-medium SPF products, an excellent SPF booster in high SPF products, oil soluble, and easily incorporated into preparations such as creams, lotions, oils, and milks.
ETHYLHEXYL SALICYLATE AT A GLANCE:
* Globally approved sunscreen agent that works primarily in the UVB range
* Commonly known as octisalate
* Helps neutralize the sun-induced formation of oxygen radicals
* Improves the stability of UV filters like oxybenzone and avobenzone
FUNCTIONS OF ETHYLHEXYL SALICYLATE IN COSMETIC PRODUCTS:
*LIGHT STABILIZER
Protecting the cosmetic product from deterioration effects of light
*UV ABSORBER
Ethylhexyl Salicylate protects the cosmetic product from damage caused by UV light
*UV FILTER
Ethylhexyl Salicylate protects skin or hair from harmful UV radiation
WHAT IS ETHYLHEXYL SALICYLATE USED FOR?
*Sun care:
Ethylhexyl salicylate is formed from salicylic acid and 2-ethylhexanol.
The salicylate part of the molecule absorbs ultraviolet light from the Sun and protects from its harmful effects
*Skin care:
The ethylhexanol part of the ethylhexyl salicylate molecule is a fatty alcohol and provides emollient and oil-like properties to the skin.
Ethylhexyl Salicylate is used to improve affinity and reduce photodegradation of other sunscreen ingredients such as oxybenzone and avobenzone.
Ethylhexyl Salicylate has superior stability than some other sunscreen active ingredients and does not produce reactive oxygen species when exposed to sunlight
ORIGIN OF ETHYLHEXYL SALICYLATE:
Ethylhexyl salicylate is an ester formed by the condensation of salicylic acid with 2-ethylhexanol.
WHAT DOES ETHYLHEXYL SALICYLATE DO IN A FORMULATION?
*Emollient
*Uv absorber
*Uv filter
SAFETY PROFILE OF ETHYLHEXYL SALICYLATE:
Ethylhexyl salicylate has a good safety profile. Although the Cosmetics Ingredient Review (CIR) notes that reproductive and developmental toxicity can occur in relation to Salicylic Acid, one of the two primary components of Ethylhexyl Salicylate, it has determined that the levels used in cosmetic and beauty products would not cause any adverse reaction. Importantly, the FDA has approved Ethylhexyl Salicylate for use in sunscreen with up to 5% concentration
ALTERNATIVE OF ETHYLHEXYL SALICYLATE:
*TITANIUM DIOXIDE
BENEFITS OF ETHYLHEXYL SALICYLATE:
*Ethylhexyl Salicylate absorbs the full range of UV-B rays.
*Ideal for water-resistant formulations.
PHYSICAL and CHEMICAL PROPERTIES of ETHYLHEXYL SALICYLATE:
CAS No.: 118-60-5
EINECS: 204-263-4
UV-B absorber: oil soluble
Molecular Weight: 250.37 g/mol
INCI name: Ethylhexyl Salicylate
USAN: Octisalate
Chemical names: 2-Ethylhexyl salicylate
Empirical Formula: C15H22O3
Single impurity >0.5%: not detectable
Sum of impurities >2.0%: not detectable
Relative density (D25/25): 1.011 – 1.016
Relative density (D20/4): 1.012 – 1.017
Refractive Index (n20/D): 1.500 – 1.503
Specific extinction E 1% ,
in methanol λ max. 305 nm: 165 – 185
Solubility at 20°C in: Readily soluble in most cosmetic oils except glycols.
Shelf life and storage conditions: 36 months in the original,
unopened container, dry, at 5 to 40°C.
Appearance: Pale yellow clear liquid (est)
Assay: 99.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 320.00 °C @ 3.40 mm Hg; 189.00 to 190.00 °C @ 21.00 mm Hg
Vapor Pressure: 0.000080 mmHg @ 25.00 °C (est)
Flash Point: > 212.00 °F TCC (> 100.00 °C)
logP (o/w): 5.934 (est)
Soluble in: Alcohol, water (0.7171 mg/L @ 25 °C est)
Insoluble in: Water
Molecular Weight: 250.33 g/mol
EINECS: 204-263-4
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
InChIKey: FMRHJJZUHUTGKE-UHFFFAOYSA-N
Merck: 6770
Flash Point: > 230 °F
Density: 1.014 g/mL at 25 °C
Refractive Index: 1.502
XLogP3: 5.7
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 8
Exact Mass: 250.15689456 g/mol
Monoisotopic Mass: 250.15689456 g/mol
Topological Polar Surface Area: 46.5 Ų
Heavy Atom Count: 18
Formal Charge: 0
Complexity: 240
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Beilstein Number: 2730664
MDL: MFCD00053300
XlogP3: 5.70 (est)
Molecular Weight: 250.33794000
Formula: C15 H22 O3
Boiling Point: 189°C
Melting Point: <25°C
Solubility: Insoluble in water
Soluble in alcohol
Chemical formula: C15H22O3
Molar mass: 250.33 g/mol
Density: 1.014 g/cm³
Melting point: < 25 °C (77 °F; 298 K)
Boiling point: 189 °C (372 °F; 462 K)
Molecular Weight: 250.33 g/mol
XLogP3: 5.7
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 8
Exact Mass: 250.15689456 Da
Monoisotopic Mass: 250.15689456 Da
Topological Polar Surface Area: 46.5 Ų
Heavy Atom Count: 18
Formal Charge: 0
Complexity: 240
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Appearance: pale yellow clear liquid (est)
Assay: 99.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 320.00 °C @ 3.40 mm Hg
Boiling Point: 189.00 to 190.00 °C @ 21.00 mm Hg
Vapor Pressure: 0.000080 mmHg @ 25.00 °C (est)
Flash Point: > 212.00 °F TCC (> 100.00 °C)
logP (o/w): 5.934 (est)
Soluble in: alcohol, water, 0.7171 mg/L @ 25 °C (est)
Insoluble in:water
Molecular Formula / Molecular Weight: C__1__5H__2__2O__3 = 250.34
Physical State (20 deg.C): Liquid
Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)
Condition to Avoid: Light Sensitive
CAS RN: 118-60-5
Reaxys Registry Number: 2730664
PubChem Substance ID: 87575896
SDBS (AIST Spectral DB): 19207
Merck Index (14): 6770
MDL Number: MFCD00053300
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
Physical state: liquid
Color: Colorless
Odor: No data available
Melting point/freezing point: < -20 °C - Regulation (EC) No. 440/2008, Annex, A.1
Initial boiling point and boiling range: 189 - 190 °C at 28 hPa - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 162 °C - closed cup - Regulation (EC) No. 440/2008, Annex, A.9
Autoignition temperature: 245 - 255 °C at 1.005 - 1.012 hPa
Decomposition temperature: No data available
pH: No data available
Viscosity:
Viscosity, kinematic: No data available
Viscosity, dynamic: 5.2 mPa.s at 40 °C
Water solubility: 0.00007 g/l at 20 °C
Partition coefficient: n-octanol/water
log Pow: 5.94 at 25 °C
Vapor pressure:
0.001 hPa at 25 °C
0.008 hPa at 50 °C
Density: 1.014 g/cm3 at 25 °C - lit.
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: None
Other safety information: No data available
Appearance at 20°C: Clear mobile liquid
Color: Colorless to pale yellow
Odor: Tends to odourless
Optical rotation (°): 0 / 0
Density at 20°C (g/ml): 1.012 - 1.020
Refractive index nd20: 1.5000 - 1.5030
Flashpoint (°C): 141
Solubility:
Solubility in water: 0.5 mg/l (20°C)
Assay (% gc): > 98
FIRST AID MEASURES of ETHYLHEXYL SALICYLATE:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available
ACCIDENTAL RELEASE MEASURES of ETHYLHEXYL SALICYLATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.
FIRE FIGHTING MEASURES of ETHYLHEXYL SALICYLATE:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.
EXPOSURE CONTROLS/PERSONAL PROTECTION of ETHYLHEXYL SALICYLATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.
HANDLING and STORAGE of ETHYLHEXYL SALICYLATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
STABILITY and REACTIVITY of ETHYLHEXYL SALICYLATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available