Quick Search
Benzyl salicylate is an ester of benzyl alcohol and salicylic acid; this ingredient has been associated with allergies and contact dermatitis.
Benzyl salicylate is a salicylic acid benzyl ester, a chemical compound most frequently used in cosmetics as a fragrance additive or UV light absorber.
Benzyl salicylate is a clear colorless liquid with a sweet floral aroma.
CAS Number: 118-58-1
EC Number: 204-262-9
Molecular Formula: C14H12O3
Molecular Weight (g/mol): 228.247
Synonyms: 2-HYDROXY- PHENYLMETHYL ESTER BENZOIC ACID, 2-HYDROXYBENZOIC ACID, BENZYL ESTER, BENZOIC ACID, 2-HYDROXY-, PHENYLMETHYL ESTER, BENZOIC ACID, 2HYDROXY, PHENYLMETHYL ESTER, BENZYL 2-HYDROXYBENZOATE, BENZYL ESTER 2-HYDROXYBENZOIC ACID, BENZYL ESTER SALICYLIC ACID, BENZYL O-HYDROXYBENZOATE, Benzyl salicylate, PHENYLMETHYL 2-HYDROXYBENZOATE, PHENYLMETHYL ESTER BENZOIC ACID, 2-HYDROXY-, SALICYLIC ACID, BENZYL ESTER, Benzyl salicylate, 118-58-1, Benzyl 2-hydroxybenzoate, Benzyl o-hydroxybenzoate, Salicylic Acid Benzyl Ester, Salicylic acid, benzyl ester, Phenylmethyl 2-hydroxybenzoate, Salicylsaeurebenzylester, NSC 6647, Salicyclic acid, benzyl ester, FEMA No. 2151, Benzoic acid, 2-hydroxy-, phenylmethyl ester, CCRIS 4749, UNII-WAO5MNK9TU, WAO5MNK9TU, 2-Hydroxybenzoic acid phenylmethyl ester, EINECS 204-262-9, Salicyclic acid benzyl ester, BRN 2115365, 2-Hydroxybenzoic acid, phenylmethyl ester, DTXSID1024598, AI3-00517, NSC-6647, Salicylic acid-benzyl ester, Benzoic acid, hydroxy-, phenylmethyl ester, DTXCID304598, HSDB 8387, EC 204-262-9, 4-10-00-00157 (Beilstein Handbook Reference), CAS-118-58-1, benzylsalicylate, benzyl salicilate, benzyl-salicylate, Benzyle salicylate, salicylic acid benzyl, Benzyl salicylate, 98%, SALICYLATE, BENZYL, WLN: QR BVO1R, SCHEMBL15573, MLS002415718, BIDD:ER0019, Benzyl salicylate [MI], CHEMBL460124, Benzyl salicylate [FCC], Benzyl salicylate [FHFI], Benzyl salicylate [INCI], FEMA 2151, NSC6647, Benzyl salicylate, >=98%, FG, CHEBI:165211, HMS2268I12, 2-Hydroxybenzoic Acid Benzyl Ester, Benzyl salicylate [WHO-DD], HY-B1556, Tox21_201869, Tox21_303046, MFCD00020034, Benzyl salicylate, analytical standard, AKOS015915010, NCGC00091411-01, NCGC00091411-02, NCGC00091411-03, NCGC00256928-01, NCGC00259418-01, AC-11580, AS-12902, SMR000112465, Benzyl salicylate, purum, >=99.0% (GC), CS-0013437, FT-0654421, S0009, A893092, Q416929, J-003850, Z19703595, InChI=1/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H, 118-58-1 [RN], 2-(HO)C6H4CO2CH2C6H5 [Formula], 204-262-9 [EINECS], 2115365 [Beilstein], 2-Hydroxybenzoic acid phenylmethyl ester, 2-Hydroxybenzoic acid, phenylmethyl ester, Benzoic acid, 2-hydroxy-, phenylmethyl ester [ACD/Index Name], benzyl 2-hydroxybenzoate, Benzyl o-hydroxybenzoate, Benzyl salicylate [ACD/IUPAC Name] [Wiki], Benzylsalicylat [German] [ACD/IUPAC Name], MFCD00020034 [MDL number], phenylmethyl 2-hydroxybenzoate, Salicyclic acid benzyl ester, Salicylate de benzyle [French] [ACD/IUPAC Name], Salicylic acid, benzyl ester, VO1750000, [118-58-1] [RN], 1219802-40-0 [RN], 2-hydroxybenzoic acid benzyl ester, 4-10-00-00157 (Beilstein Handbook Reference) [Beilstein], Benzoic acid, hydroxy-, phenylmethyl ester, benzyl 2-hydroxybenzoate, Benzyl O-Hydroxybenzene, BENZYL SALICILATE, Benzyl salicylate-d4, Benzyle salicylate, benzyl-salicylate, Benzylsalicylate, EINECS 204-262-9, NCGC00091411-02, QR BVO1R [WLN], salicylic acid benzyl ester, Salicylic acid-benzyl ester, Salicylsaeurebenzylester, ST5405469, WLN: QR BVO1R
Benzyl salicylate is a constituent of raw propolis that can be identified by headspace solid-phase microextraction (HS-SPME), followed by gas chromatography-mass spectrometry (GC-MS).
Benzyl salicylate is a chemical compound most frequently used in cosmetics.
Benzyl salicylate is also used as a solvent for synthetic musks and as a preservative in floral compositions such as Jasmine, Liliac, and Lily.
Benzyl salicylate, a salicylic acid benzyl ester, can be used as a component in perfumes and as a solvent for crystalline synthetic musks.
Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
Benzyl 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.
Benzyl salicylate is used by consumers, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Benzyl salicylate is a clear colorless liquid with a sweet floral aroma.
In cosmetics and personal care products, Benzyl salicylate is used in the formulation of bath products, bubble baths, cleansing products, hair care products, makeup, moisturizers, perfumes and colognes, shampoos, skin care products and suntan products.
Benzyl salicylate is a salicylic acid benzyl ester, a chemical compound most frequently used in cosmetics.
Benzyl salicylate appears as an almost colorless liquid with a mild odor described as "very faint, sweetfloral, slightly balsamic" by those who can smell it, but many people either can't smell Benzyl salicylate at all or describe Benzyl salicylate smell as "musky".
Trace impurities can have a significant influence on the odour.
Benzyl salicylate occurs naturally in a variety of plants and plant extracts and is widely used in blends of fragrance materials.
There is some evidence that people can become sensitized to Benzyl salicylate and as a result there is a restriction standard concerning the use of Benzyl salicylate in fragrances by the International Fragrance Association.
Benzyl salicylate is used as a solvent for crystalline synthetic musks and as a component and fixative in floral perfumes such as carnation, jasmine, lilac, and wallflower.
Benzyl salicylate is a colorless liquid.
Benzyl salicylate is melting point is near room temperature.
Benzyl salicylate is a benzoate ester and a member of phenols.
Benzyl salicylate is functionally related to a salicylic acid.
Benzyl salicylate is a salicylic acid benzyl ester, a chemical compound most frequently used in cosmetics as a fragrance additive or UV light absorber.
Benzyl salicylate appears as an almost colorless liquid with a mild odor described as "very faint, sweet-floral, slightly balsamic" by some, while others smell nothing at all.
There is debate whether the odour is caused solely by impurities or a genetic predisposition.
Benzyl salicylate occurs naturally in a variety of plants and plant extracts and is widely used in blends of fragrance materials.
There is some evidence that people may become sensitized to Benzyl salicylate and as a result, there is a restriction standard concerning the use of Benzyl salicylate in fragrances by the International Fragrance Association.
Benzyl salicylate is used as a solvent for crystalline synthetic musks and as a component and fixative in floral perfumes such as carnation, jasmine, lilac, and wallflower.
Benzyl salicylate has a fresh, sweet, balsam tone.
Benzyl salicylate is clean, herbal oily, with touches of soft-narcotic and frangipanni.
Benzyl salicylate is aromatic, slightly-medicinal, and has qualities of orchid petal and faint sweet-florals.
Benzyl salicylate is, according to the judgment of some people, (including perfumers) absolutely odorless while others find Benzyl salicylate 'musky' of odor Trace impurities can greatly influence the odor of this high-boiling chemical
Benzyl salicylate is sweet, balsamic herbal oily aroma chemical with soft-narcotic touches.
Benzyl salicylate is a commonly used perfumery chemical.
Benzyl salicylate is an aromatic chemical, usually appearing as a clear liquid with a mild sweet floral odour.
This compound appears as a component of some of our fragrance blends.
Benzyl salicylate is a synthetic chemical produced for industry from benzyl alcohol and salicylic acid, however Benzyl salicylate can be found naturally in some plants and plant extracts, such as hyacinth flower oil and ylang-ylang oil.
Benzyl salicylate's used as a fixative and solvent in cosmetic fragrances, and is also used in some sunscreens for Benzyl salicylate UV light absorbing properties.
Applications of Benzyl salicylate:
Benzyl salicylate is a clear almost colourless liquid that has a mild balsamic, sweetly floral note possessing excellent blending capabilities.
Often used for Benzyl salicylate ‘cosmetic notes’ as a base for heavy florals such as ylang, gardenia, jasmine, lily etc.
Benzyl salicylate is also used in functional products such as soap, shampoo and fabric softener.
Uses of Benzyl salicylate:
Benzyl salicylate is a fragrance found naturally occurring in carnations and in certain members of the primrose family.
Although Benzyl salicylate can be derived for cosmetic use from natural essential oils, such as jasmine oil, neroli, and ylang-ylang, Benzyl salicylate can also be synthetically manufactured.
Benzyl salicylate is an chemical compound commonly used in the cosmetic industry.
Benzyl salicylate is also found in essential oils from green tea and was shown to exhibit antioxidant and antimicrobia l activity.
Benzyl salicylate is used as a fixer in perfumery; in sunscreen preparations.
Benzyl salicylate is used in perfume fixative, solvent for synthetic musk, sunscreening lotions, soap odorant.
Benzyl salicylate is used as a fixative and solvent for nitro musks and as a fragrance for detergents.
Benzyl salicylate is widely used in soap and cosmetic industry as fragrance; also effective in absorbing UV light, and can be used in protective sunscreen lotions.
Benzyl salicylate is also used in deodorant sprays.
Consumer Uses:
Benzyl salicylate is used in the following products: washing & cleaning products, air care products, biocides (e.g. disinfectants, pest control products), polishes and waxes, perfumes and fragrances and cosmetics and personal care products.
Other release to the environment of Benzyl salicylate is likely to occur from: indoor use as processing aid and outdoor use as processing aid.
Other Consumer Uses:
Fragrance
Odor agents
Widespread uses by professional workers:
Benzyl salicylate is used in the following products: polishes and waxes, washing & cleaning products, air care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, cosmetics and personal care products and welding & soldering products.
Uses at industrial sites:
Benzyl salicylate is used in the following products: washing & cleaning products, air care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, polishes and waxes and cosmetics and personal care products.
Industry Uses:
Flavoring and nutrient
Fragrance
Odor agents
Manufacturing Methods of Benzyl salicylate:
Benzyl salicylate is manufacturing by esterification of salicylic acid with benzyl alcohol.
Benzyl salicylate can be manufactured by reacting benzyl chloride with an alkali salicylate or by the transesterification of methyl salicylate with benzyl alcohol.
General Manufacturing Information of Benzyl salicylate:
Industry Processing Sectors:
All Other Basic Organic Chemical Manufacturing
All Other Chemical Product and Preparation Manufacturing
Food, beverage, and tobacco product manufacturing
Other (requires additional information)
Pesticide, Fertilizer, and Other Agricultural Chemical Manufacturing
Plastics Material and Resin Manufacturing
Soap, Cleaning Compound, and Toilet Preparation Manufacturing
Wholesale and Retail Trade
Identification of Benzyl salicylate:
Analytic Laboratory Methods:
The European legislation on cosmetic products has recently required the declaration of 26 compounds (24 volatile chemicals and 2 natural extracts) on the label of final products when exceeding a stipulated cut-off level.
In this work a rapid reliable and specific RP-HPLC method coupled with diode array detector (DAD) has been developed for the simultaneous determination and quantification of the 24 volatile chemicals: amyl cinnamal, benzyl alcohol, cinnamyl alcohol, citral, eugenol, hydroxy-citronellal, isoeugenol, amylcinnamyl alcohol, Benzyl salicylate, cinnamal, coumarin, geraniol, Lyral (hydroxy-methylpentylcyclohexene carboxaldehyde), anisyl alcohol, benzyl cinnamate, farnesol, Lilial (2-(4-tert-butylbenzyl)propionaldehyde) linalool, benzyl benzoate, citronellol, hexyl cinnamal, limonene, methylheptin carbonate, alpha-isomethyl ionone (3-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one).
The 24 analytes were appropriately separated over a running time of 40 min, on a C18 column using a simple gradient elution (acetonitrile/water) with flow rate from 0.7 to 1.0 mL/min and UV acquisition at 210, 254 and 280 nm.
All calibration curves showed good linearity (r2>0.99) within test ranges.
The method was successfully applied to the qualitative and quantitative determination of the potential allergens in four commercial scented products, with satisfactory accuracy and precision.
The results indicated that this simple and efficient method can be used for quality assessment of complex matrices such us cosmetic scented products.
In the present work, a strategy for the qualitative and quantitative analysis of 24 volatile compounds listed as suspected allergens in cosmetics by the European Union is reported.
The list includes benzyl alcohol, limonene, linalool, methyl 2-octynoate, beta-citronellol, geraniol, citral (two isomers), 7-hydroxycitronellal, anisyl alcohol, cinnamal, cinnamyl alcohol, eugenol, isoeugenol (two isomers), coumarin, alpha-isomethyl ionone, lilial, alpha-amylcinnamal, lyral, alpha-amylcinnamyl alcohol, farnesol (three isomers), alpha-hexyl cinnamal, benzyl cinnamate, benzyl benzoate, and Benzyl salicylate.
The applicability of a headspace (HS) autosampler in combination with a gas chromatograph (GC) equipped with a programmable temperature vaporizer (PTV) and a quadrupole mass spectrometry (qMS) detector is explored.
By using a headspace sampler, sample preparation is reduced to introducing the sample into the vial.
This reduces the analysis time and the experimental errors associated with this step of the analytical process.
Two different injection techniques were used: solvent-vent injection and hot-split injection.
The first offers a way to improve sensitivity at the same time maintaining the simple headspace instrumentation and Benzyl salicylate is recommended for compounds at trace levels.
The use of a liner packed with Tenax-TA allowed the compounds of interest to be retained during the venting process.
The signals obtained when hot-split injection was used allowed quantification of all the compounds according to the thresholds of the European Cosmetics Directive.
Monodimensional gas chromatography coupled to a conventional quadrupole mass spectrometry detector was used and the 24 analytes were separated appropriately along a run time of about 12 min.
Use of the standard addition procedure as a quantification technique overcame the matrix effect.
Benzyl salicylate should be emphasized that the method showed good precision and accuracy.
Furthermore, Benzyl salicylate is rapid, simple, and - in view of the results - highly suitable for the determination of suspected allergens in different cosmetic products.
The study objective was/ to analyze the chemical constituents of volatile oil from flowers of Rhododendron mucronatum.
The volatile oil was extracted by water-steam distillation and analyzed by GC-MS.
Forty-nine compounds, which occupied 79.55% of total constituents, were identified.
The major constituents were linalool, beta-eudesmene, phytol, benzyl benzoate, Benzyl salicylate and nonyl aldehyde.
The chemical constituents of volatile oil, which contain many bioactive constituents, are mainly composed of terpenes, esters, and alkanes.
In this study, a novel and efficient method based on headspace solid-phase microextraction (HS-SPME), followed by gas chromatography-mass spectrometry (GC-MS), was developed for the analysis of propolis volatile compounds.
The HS-SPME procedure, whose experimental parameters were properly optimized, was carried out using a 100 um polydimethylsiloxane (PDMS) fiber.
The GC-MS analyses were performed on a HP-5 MS cross-linked 5% diphenyl-95% dimethyl polysiloxane capillary column (30 m x 0.25 mm I.D., 1.00 um film thickness), under programmed-temperature elution.
Ninety-nine constituents were identified using this technique in the samples of raw propolis collected from different Italian regions.
The main compounds detected include benzoic acid (0.87-30.13%) and Benzyl salicylate esters, such as benzyl benzoate (0.16-13.05%), Benzyl salicylate (0.34-1.90%) and benzyl cinnamate (0.34-3.20%).
Vanillin was detected in most of the samples analyzed in this study (0.07-5.44%).
Another relevant class of volatile constituents is represented by sesquiterpene hydrocarbons, such as delta-cadinene (1.29-13.31%), gamma-cadinene (1.36-8.85%) and alpha-muurolene (0.78-6.59%), and oxygenated sesquiterpenes, such as beta-eudesmol (2.33-12.83%), T-cadinol (2.73-9.95%) and alpha-cadinol (4.84-9.74%).
Regarding monoterpene hydrocarbons, they were found to be present at low level in the samples analyzed in this study, with the exception of one sample from Southern Italy, where alpha-pinene was the most abundant constituent (13.19%).
The results obtained by HS-SPME-GC-MS were also compared with those of hydrodistillation (HD) coupled with GC-MS.
The HS-SPME-GC-MS method developed in this study allowed us to determine the chemical fingerprint of propolis volatile constituents, thus providing a new and reliable tool for the complete characterization of this biologically active apiary product.
Clinical Laboratory Methods of Benzyl salicylate:
UV-filters are widely used in many personal care products and cosmetics.
Recent studies indicate that some organic UV-filters can accumulate in biota and act as endocrine disruptors, but there are few studies on the occurrence and fate of these compounds in humans.
In the present work, a new liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to assess the presence of six UV-filters in current use (Benzyl salicylate, phenyl salicylate, octyl salicylate, homosalate, 3-(4-methylbenzylidene) camphor, and 3-benzylidene camphor) in human placental tissue is proposed.
The method involves the extraction of the analytes from the samples using ethyl acetate, followed by a clean-up step using centrifugation prior to their quantification by LC-MS/MS using an atmospheric pressure chemical ionization (APCI) interface.
Bisphenol A-d16 was used as surrogate for the determination of Benzyl salicylate, phenyl salicylate, octyl salicylate and homosalate in negative mode and benzophenone-d10, was used as surrogate for the determination of 3-(4-methylbenzylidene) camphor and 3-benzylidene camphor in positive mode.
The found limits of detection ranged from 0.4 to 0.6 ng/g and the limits of quantification ranged from 1.3 to 2.0 ng/g, while variability was under 13.7%.
Recovery rates for spiked samples ranged from 97% to 104%.
Moreover, the interactions of these compounds with the human estrogen receptor alpha (hERalpha) and androgen receptor (hAR), using two in vitro bioassays based on reporter gene expression and cell proliferation assessment, were also investigated.
All tested compounds, except Benzyl salicylate and octyl salicylate, showed estrogenic activity in the E-Screen bioassay whereas only homosalate and 3-(4-methylbenzylidene) camphor were potent hAR antagonists.
Although free salicylate derivatives and free camphor derivatives were not detected in the human placenta samples analyzed, the observed estrogenic and anti-androgenic activities of some of these compounds support the analysis of their occurrence and their role as endocrine disrupters in humans.
Chemical Properties of Benzyl salicylate:
Benzyl salicylate has a faint, sweet, floral odor and a sweet, currant-like taste.
Benzyl salicylate occurs in several essential oils, is a colorless, viscous liquid with a weak, sweet, slightly balsamic odor.
Occurrence of Benzyl salicylate:
Benzyl salicylate has been reported in small amounts in carnation oil (Dianthus caryophyllus L.) and in larger amounts in the oil of Primula auricula.
Also found in American cranberry, clove bud, peppermint oil and buckwheat.
Handling and Storage of Benzyl salicylate:
Nonfire Spill Response:
SMALL SPILLS AND LEAKAGE:
If you spill this chemical, use absorbent paper to pick up all liquid spill material.
Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal.
Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution.
Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
STORAGE PRECAUTIONS:
You should store this chemical under refrigerated temperatures and away from mineral acids and bases.
Storage Conditions of Benzyl salicylate:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Reactivity Profile of Benzyl salicylate:
Benzyl salicylate may hydrolyze in aqueous acid or basic solutions.
Benzyl salicylate can react with oxidizing materials.
Presents no significant reactivity hazard, by itself or in contact with water.
Chemical stability:
Good stability under normal storage conditions.
Possibility of hazardous reactions:
Not expected under normal conditions of use.
Conditions to avoid:
Avoid extreme heat.
Incompatible materials:
Avoid contact with strong acids, alkalis or oxidising agents.
Hazardous decomposition products:
Not expected.
First Aid Measures of Benzyl salicylate:
EYES:
First check the victim for contact lenses and remove if present.
Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center.
Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician.
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
SKIN:
IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing.
Gently wash all affected skin areas thoroughly with soap and water.
If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.
INHALATION:
IMMEDIATELY leave the contaminated area; take deep breaths of fresh air.
If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital.
Provide proper respiratory protection to rescuers entering an unknown atmosphere.
Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.
INGESTION:
DO NOT INDUCE VOMITING.
If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center.
Be prepared to transport the victim to a hospital if advised by a physician.
If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body.
DO NOT INDUCE VOMITING.
IMMEDIATELY transport the victim to a hospital.
Fire Fighting of Benzyl salicylate:
To extinguish a fire involving this chemical you may use a dry chemical, carbon dioxide, foam or halon extinguisher; a water spray may also be used.
Fire Fighting Procedures of Benzyl salicylate:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Advice for firefighters:
Wear self contained breathing apparatus for fire fighting if necessary.
Accidental Release Measures of Benzyl salicylate:
Cleanup Methods:
Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.
Avoid breathing vapors, mist or gas.
Ensure adequate ventilation.
Evacuate personnel to safe areas.
Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.
Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.
Disposal Methods of Benzyl salicylate:
Recycle any unused portion of Benzyl salicylate for Benzyl salicylate approved use or return Benzyl salicylate to the manufacturer or supplier.
Ultimate disposal of the chemical must consider:
Benzyl salicylate's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations.
If Benzyl salicylate is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of Benzyl salicylate; Contaminated packaging: Dispose of as unused product.
Identifiers of Benzyl salicylate:
Synonym(s): Benzyl 2-hydroxybenzoate
Linear Formula: 2-(HO)C6H4CO2CH2C6H5
CAS Number: 118-58-1
Molecular Weight: 228.24
Beilstein: 2115365
EC Number: 204-262-9
MDL number: MFCD00020034
eCl@ss: 39024514
PubChem Substance ID: 24847092
NACRES: NA.22
Product Number: S0009
Purity / Analysis Method: >99.0%(GC)
Molecular Formula / Molecular Weight: C14H12O3 = 228.25
Physical State (20 deg.C): Liquid
CAS RN: 118-58-1
Reaxys Registry Number: 2115365
PubChem Substance ID: 87575640
SDBS (AIST Spectral DB): 1711
Merck Index (14): 1144
MDL Number: MFCD00020034
CAS: 118-58-1
Molecular Formula: C14H12O3
Molecular Weight (g/mol): 228.247
MDL Number: MFCD00020034
InChI Key: ZCTQGTTXIYCGGC-UHFFFAOYSA-N
PubChem CID: 8363
IUPAC Name: benzyl 2-hydroxybenzoate
SMILES: C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O
CAS Number: 118-58-1
ChEMBL: ChEMBL460124
ChemSpider: 8060
ECHA InfoCard: 100.003.876
PubChem CID: 8363
UNII: WAO5MNK9TU
CompTox Dashboard (EPA): DTXSID1024598
InChI:
InChI=1S/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H2
Key: ZCTQGTTXIYCGGC-UHFFFAOYSA-N
InChI=1/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H2
Key: ZCTQGTTXIYCGGC-UHFFFAOYAC
SMILES: O=C(OCc1ccccc1)c2ccccc2O
Properties of Benzyl salicylate:
Chemical formula: C14H12O3
Molar mass: 228.247 g·mol−1
Appearance: Colorless liquid
Density: 1.17 g/cm3
Molecular Weight: 228.24 g/mol
XLogP3: 3.2
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 4
Exact Mass: 228.078644241 g/mol
Monoisotopic Mass: 228.078644241 g/mol
Topological Polar Surface Area: 46.5Ų
Heavy Atom Count: 17
Complexity: 246
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Assay: 98%
refractive index: n20/D 1.581 (lit.)
bp: 168-170 °C/5 mmHg (lit.)
density: 1.176 g/mL at 25 °C (lit.)
SMILES string: Oc1ccccc1C(=O)OCc2ccccc2
InChI: 1S/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H2
InChI key: ZCTQGTTXIYCGGC-UHFFFAOYSA-N
Specifications of Benzyl salicylate:
Melting Point: 18°C to 20°C
Density: 1.17
Boiling Point: 190°C (14mmHg)
Flash Point: 137°C (278°F)
Refractive Index: 1.5804
Quantity: 100 g
Beilstein: 2115365
Merck Index: 14,1144
Formula Weight: 228.25
Percent Purity: 99%
Chemical Name or Material: Benzyl salicylate
Names of Benzyl salicylate:
Regulatory process names:
Benzoic acid, 2-hydroxy-, phenylmethyl ester
Benzyl o-hydroxybenzoate
Benzyl salicylate
Benzyl salicylate
Benzyl salicylate
Phenylmethyl 2-hydroxybenzoate
Salicyclic acid, benzyl ester
Salicylic acid, benzyl ester
Salicylsaeurebenzylester
Translated names:
bensylsalicylat (sv)
Bensüülsalitsülaat (et)
bentsyylisalisylaatti (fi)
benzil saliċilat (mt)
benzil-szalicilát (hu)
benzilsalicilat (hr)
benzilsalicilat (sl)
benzilsalicilatas (lt)
benzilsalicilāts (lv)
benzyl-2-hydroxybenzoát (sk)
benzyl-salicylát (cs)
benzylsalicylaat (nl)
benzylsalicylat (da)
Benzylsalicylat (de)
salicilat de benzil (ro)
Salicilato de bencilo (es)
salicilato de benzilo (pt)
salicilato di benzile (it)
salicylan benzylu (pl)
Salicylate de benzyle (fr)
σαλικυλικό βένζυλο (el)
бензилов салицилат (bg)
IUPAC names:
2-hydroxybenzoic acid phenylmethyl ester
Benzoic acid, 2-hydroxy-, phenylmethyl ester
benzyl 2-hydroxybenzoaat
Benzyl 2-hydroxybenzoate
benzyl 2-hydroxybenzoate
Benzyl 2-hydroxybenzoateBenzyl salicylate
benzyl salicilate
Benzyl salicylate
Benzyl salicylate
Benzyl salicylate
Benzyl salicylate
Benzyl salicylate
Benzyl salicylate
Benzyl salicylate
Benzyl-2 hydroxibensoate
Benzylsalicylat
phenylmethyl 2-hydroxybenzoate
Salicylic acid, benzylester
Preferred IUPAC name:
Benzyl 2-hydroxybenzoate
Trade names:
Benzyl 2-hydroxybenzoate
Benzyl o-hydroxybenzoate
Benzyl salicylate
Benzyl salicylate
Phenylmethyl 2-hydroxybenzoate
Salicylic acid, benzyl ester
Other identifiers:
118-58-1
607-754-00-5
