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· · COA & SDS available for every product · Same-day shipping on in-stock items 4-Benzylphenol - ≥97%(GC) , CAS No.101-53-1
Synonyms
NCGC00258562-01 | Parabencilfenilcarbamato [Spanish] | MFCD00002384 | 4-benzyiphenol | NSC8078 | NSC-8078 | STL066603 | p-Cresol, .alpha.-phenyl- | NCGC00248895-02 | H0239 | p-Benzylphenol | P-BENZYLPHENOL [MI] | BENZYL-P-PHENOL | UNII-CS02509J25 | .alpha
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Why this grade ≥97%(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.
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Literature proof Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
NCGC00258562-01 | Parabencilfenilcarbamato [Spanish] | MFCD00002384 | 4-benzyiphenol | NSC8078 | NSC-8078 | STL066603 | p-Cresol, .alpha.-phenyl- | NCGC00248895-02 | H0239 | p-Benzylphenol | P-BENZYLPHENOL [MI] | BENZYL-P-PHENOL | UNII-CS02509J25 | .alpha
Specifications & Purity
≥97%(GC)
Names and Identifiers Pubchem Sid 488180483 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180483 Canonical Smiles C1=CC=C(C=C1)CC2=CC=C(C=C2)O IUPAC Name 4-benzylphenol InChIKey HJSPWKGEPDZNLK-UHFFFAOYSA-N INCHI 1S/C13H12O/c14-13-8-6-12(7-9-13)10-11-4-2-1-3-5-11/h1-9,14H,10H2 Isomeric SMILES C1=CC=C(C=C1)CC2=CC=C(C=C2)O WGK Germany 2 RTECS SM8330500 Molecular Weight 184.24 Beilstein 6675 Reaxy-Rn 1449572 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1449572&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 Kingdom Organic compounds Superclass Benzenoids Class Benzene and substituted derivatives Subclass Diphenylmethanes Intermediate Tree Nodes Not available Direct Parent Diphenylmethanes Alternative Parents 1-hydroxy-2-unsubstituted benzenoids Organooxygen compounds Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Diphenylmethane - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Boil Point(°C) 320-322°C Melt Point(°C) 79-85°C Molecular Weight 184.230 g/mol XLogP3 3.500 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 2 Exact Mass 184.089 Da Monoisotopic Mass 184.089 Da Topological Polar Surface Area 20.200 Ų Heavy Atom Count 14 Formal Charge 0 Complexity 153.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Citations of This Product References 1. Zong-Pin Fu, Yun-Peng Zhao, Yu-Fa Wu, Qi-Jie Zhou, Shu-Ting Hu, Le-Le Qiu, Fang-Jing Liu, Mei Zhong, Jing Liang, Jing-Pei Cao. (2026) Interfacial oxygen vacancies and Cu-Ni bimetallic sites synergistically enhance the catalytic hydroconversion of soluble portion from lignite thermal dissolution. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, [PMID: [10.1016/j.jaap.2026.107623 ]
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