Phenylglyoxal monohydrate - ≥97%(GC) , CAS No.1074-12-0

CAS: 1074-12-0 Cat. No.: P165810 Molecular Weight: 152.15 EC Number: 214-036-1 PubChem CID: 14090
AVAILABLE TO ORDER
GRADE & PURITY ≥97%(GC)
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
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
P165810-1g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$21.90

$32.90
Save $11.00 (33.43%)
5g
P165810-5g
3

$61.90

$92.90
Save $31.00 (33.37%)
25g
P165810-25g
2

$232.90

$349.90
Save $117.00 (33.44%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

📋

Quality documents

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

📚

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
Shipped In
Normal
Purity
≥97%(GC)
Names and Identifiers
Pubchem Sid488181938
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181938
Canonical SmilesC1=CC=C(C=C1)C(=O)C=O
IUPAC Name2-oxo-2-phenylacetaldehyde
InChIKeyOJUGVDODNPJEEC-UHFFFAOYSA-N
INCHI1S/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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassPhenylacetaldehydes
Intermediate Tree Nodes Not available
Direct ParentPhenylacetaldehydes
Alternative Parents Benzoyl derivatives  Aryl ketones  Alpha ketoaldehydes  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACLY Tclin ATP-citrate synthase (168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Agrobacterium tumefaciens (620 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.

8 results found

Lot NumberCertificate TypeDateItem
F2605084Certificate of AnalysisJun 15, 2026 P165810
C2625106Certificate of AnalysisApr 07, 2026 P165810
G2222582Certificate of AnalysisFeb 04, 2026 P165810
G2222583Certificate of AnalysisFeb 04, 2026 P165810
J2514080Certificate of AnalysisOct 17, 2025 P165810
C2505755Certificate of AnalysisMar 08, 2025 P165810
G2514416Certificate of AnalysisApr 15, 2024 P165810
K2125290Certificate of AnalysisSep 11, 2023 P165810
Chemical and Physical Properties
Sensitivityair sensitive
Melt Point(°C)~76°C
Molecular Weight134.130 g/mol
XLogP31.700
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass134.037 Da
Monoisotopic Mass134.037 Da
Topological Polar Surface Area34.100 Ų
Heavy Atom Count10
Formal Charge0
Complexity134.000
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. 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]
Solution Calculators
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