Benzyl Salicylate - ≥99%(GC) , CAS No.118-58-1

CAS: 118-58-1 Cat. No.: B153106 Molecular Weight: 228.25 Beilstein Registry Number: 2115370 EC Number: 204-262-9
AVAILABLE TO ORDER
GRADE & PURITY ≥99%(GC)
Synonyms
2-Hydroxybenzoic acid phenylmethyl ester | BRN 2115365 | Phenylmethyl 2-hydroxybenzoate | SCHEMBL15573 | NCGC00256928-01 | BENZYL SALICYLATE [FHFI] | FEMA No. 2151 | J-003850 | Benzyl salicylate, 98% | EINECS 204-262-9 | Salicylic acid-benzyl ester | BENZ
Storage
Room temperature
Shipped In
Normal
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Size
Status
Price
Qty
5g
B153106-5g
3
$9.90
25g
B153106-25g
5
$10.90
100g
B153106-100g
4

$13.90

$20.90
Save $7.00 (33.49%)
500g
B153106-500g
1

$40.90

$61.90
Save $21.00 (33.93%)
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Why this grade

≥99%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

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).

Specifications

Synonyms
2-Hydroxybenzoic acid phenylmethyl ester | BRN 2115365 | Phenylmethyl 2-hydroxybenzoate | SCHEMBL15573 | NCGC00256928-01 | BENZYL SALICYLATE [FHFI] | FEMA No. 2151 | J-003850 | Benzyl salicylate, 98% | EINECS 204-262-9 | Salicylic acid-benzyl ester | BENZ
Specifications & Purity
≥99%(GC)
Storage
Room temperature
Shipped In
Normal
Purity
≥99%(GC)
Names and Identifiers
Pubchem Sid488180764
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180764
Canonical SmilesC1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O
IUPAC Namebenzyl 2-hydroxybenzoate
InChIKeyZCTQGTTXIYCGGC-UHFFFAOYSA-N
INCHI1S/C14H12O3/c15-13-9-5-4-8-12(13)14(16)17-10-11-6-2-1-3-7-11/h1-9,15H,10H2
Isomeric SMILES C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O
WGK Germany 2
RTECS VO1750000
Molecular Weight 228.25
Beilstein 2115370
Reaxy-Rn 2115365
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2115365&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Benzoic acid esters
Direct Parento-Hydroxybenzoic acid esters
Alternative Parents Salicylic acid and derivatives  Benzyloxycarbonyls  Benzoyl derivatives  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Vinylogous acids  Carboxylic acid esters  Monocarboxylic acids and derivatives  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents O-hydroxybenzoic acid ester - Benzyloxycarbonyl - Salicylic acid or derivatives - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous acid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Dermatophagoides pteronyssinus (58 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis C virus (23859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tribolium castaneum (596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot NumberCertificate TypeDateItem
I2214164Certificate of AnalysisJun 15, 2026 B153106
K2104292Certificate of AnalysisAug 12, 2025 B153106
I2504912Certificate of AnalysisApr 25, 2024 B153106
I2504915Certificate of AnalysisApr 25, 2024 B153106
C2317041Certificate of AnalysisMar 21, 2023 B153106
B2518065Certificate of AnalysisMar 18, 2023 B153106
E23121239Certificate of AnalysisMar 18, 2023 B153106
E23121242Certificate of AnalysisMar 18, 2023 B153106
E23121243Certificate of AnalysisMar 18, 2023 B153106
E23121244Certificate of AnalysisMar 18, 2023 B153106
E23121251Certificate of AnalysisMar 18, 2023 B153106
E23121252Certificate of AnalysisMar 18, 2023 B153106
B2310365Certificate of AnalysisFeb 15, 2023 B153106
B2625202Certificate of AnalysisJul 30, 2021 B153106
K2411049Certificate of AnalysisJul 30, 2021 B153106

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Chemical and Physical Properties
SolubilitySlightly soluble in water, miscible with ether and alcohol
Refractive Index1.5804
Flash Point(°F)356 °F
Flash Point(°C)184°C
Boil Point(°C)194°C
Melt Point(°C)18-20℃
Molecular Weight228.240 g/mol
XLogP33.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass228.079 Da
Monoisotopic Mass228.079 Da
Topological Polar Surface Area46.500 Ų
Heavy Atom Count17
Formal Charge0
Complexity246.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Kaige Zhang, Shuangying Li, Yunhe Wang, Jing Fan, Guifen Zhu.  (2020)  Air-assisted liquid-liquid microextraction based on solidification of floating deep eutectic solvent for the analysis of ultraviolet filters in water samples by high performance liquid chromatography with the aid of response surface methodology.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:31980262] [10.1016/j.chroma.2020.460876]
2. Cheng Jie, Kong Xiaojian, Liu Shucheng, Che Dandan, Sun Zhiwei, Li Guoliang, Ping Meiling, Tang Jingpu, You Jinmao.  (2018)  Determination of Ultraviolet Filters in Domestic Wastewater by LC–MS Coupled with Polydopamine-Based Magnetic Solid-Phase Extraction and Isotope-Coded Derivatization.  CHROMATOGRAPHIA,  81  (12): (1673-1684).  [PMID:] [10.1007/s10337-018-3650-x]
3. Zhu Bao, Zhang Yanjun, Gao Rong, Wu Zhihua, Zhang Wei, Zhang Chao, Zhang Penghong, Ye Can, Yao Linbo, Jin Ying, Mao Hui, Tou Peiyao, Huang Peng, Zhao Jiangzhe, Zhao Qiao, Liu Chang-Jun, Zhang Kewei.  (2025)  Complete biosynthesis of salicylic acid from phenylalanine in plants.  NATURE,      [PMID:40702181] [10.1038/s41586-025-09175-9]
Solution Calculators
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