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224,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items Phenylglyoxal monohydrate - ≥97%(GC) , CAS No.1074-12-0
Synonyms
NSC156299 | NSC-156299 | NCGC00091619-02 | 2-oxo-2-phenylacetaldehyde | 2-oxo-2-phenyl-acetaldehyde | N45G3015PA | Q5934181 | alpha-oxobenzeneacetaldehyde | FT-0633297 | AKOS009031532 | NCGC00091619-01 | O10845 | Z1954804411 | Benzeneacetaldehyde, a-oxo-
Storage
Argon charged,Room temperature
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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 Argon charged,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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Specific reagent for arginine.
Specifications Synonyms
NSC156299 | NSC-156299 | NCGC00091619-02 | 2-oxo-2-phenylacetaldehyde | 2-oxo-2-phenyl-acetaldehyde | N45G3015PA | Q5934181 | alpha-oxobenzeneacetaldehyde | FT-0633297 | AKOS009031532 | NCGC00091619-01 | O10845 | Z1954804411 | Benzeneacetaldehyde, a-oxo-
Specifications & Purity
≥97%(GC)
Storage
Argon charged, Room temperature
Names and Identifiers Pubchem Sid 488181938 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488181938 Canonical Smiles C1=CC=C(C=C1)C(=O)C=O IUPAC Name 2-oxo-2-phenylacetaldehyde InChIKey OJUGVDODNPJEEC-UHFFFAOYSA-N INCHI 1S/C8H6O2/c9-6-8(10)7-4-2-1-3-5-7/h1-6H Isomeric SMILES C1=CC=C(C=C1)C(=O)C=O WGK Germany 3 RTECS MD3260000 Alternate CAS 78146-52-8 PubChem CID 14090 Molecular Weight 152.15
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 Phenylacetaldehydes Intermediate Tree Nodes Not available Direct Parent Phenylacetaldehydes Alternative Parents Benzoyl derivatives Aryl ketones Alpha ketoaldehydes Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Phenylacetaldehyde - Aryl ketone - Benzoyl - Alpha-ketoaldehyde - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as phenylacetaldehydes. These are compounds containing a phenylacetaldehyde moiety, which consists of a phenyl group substituted at the second position by an acetalydehyde. External Descriptors a small molecule 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 Sensitivity air sensitive Melt Point(°C) ~76°C Molecular Weight 134.130 g/mol XLogP3 1.700 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 2 Exact Mass 134.037 Da Monoisotopic Mass 134.037 Da Topological Polar Surface Area 34.100 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 134.000 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. Xie Chao, Lin Longfei, Huang Liang, Wang Zixin, Jiang Zhiwei, Zhang Zehui, Han Buxing. (2021) Zn-Nx sites on N-doped carbon for aerobic oxidative cleavage and esterification of C(CO)-C bonds. Nature Communications, 12 (1): (1-12). [PMID:34376654 ] [10.1038/s41467-021-25118-0 ] 2. Hong Pan, Qi Luo, Qiuyi Jing, Lin Chen, Ni Li, Chao Fang, Fuguo Shi. (2025) Multiple endogenous aldehydes amplify acetaminophen-induced liver injury. CHEMICO-BIOLOGICAL INTERACTIONS, [PMID:40562332 ] [10.1016/j.cbi.2025.111619 ]
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