Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	38835
Common Name:	Phenylacetaldehyde
Systematic Name:	2-phenylacetaldehyde
RefMet Name:	Phenylacetaldehyde
Synonyms:	[PubChem Synonyms]
Exact Mass:	120.0575 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C8H8O
InChIKey:	DTUQWGWMVIHBKE-UHFFFAOYSA-N
ClassyFire superclass:	Benzenoids [C0002448]
ClassyFire class:	Benzene and substituted derivatives [C0002279]
ClassyFire subclass:	Phenylacetaldehydes [C0001257]
ClassyFire direct parent:	Phenylacetaldehydes [C0001257]
Massbank MS spectra:	View MS spectra
SMILES:	c1ccc(cc1)CC=O
Studies:	Available studies (via RefMet name)

Select appropriate tab below to view additional details:

All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	998
CHEBI ID:	16424
HMDB ID:	HMDB0006236
KEGG ID:	C00601
Chemspider ID:	13876539
BMRB ID:	bmse000427
MetaCyc ID:	PHENYLACETALDEHYDE
EPA CompTox DB:	DTXCID501483
Plant Metabolite Hub(Pmhub):	MS000006847

Calculated physicochemical properties (?):

Heavy Atoms:	9
Rings:	1
Aromatic Rings:	1
Rotatable Bonds:	2
van der Waals Molecular volume:	121.93 Å3 molecule-1
Toplogical Polar Sufrace Area:	17.07 Å2 molecule-1
Hydrogen Bond Donors:	0
Hydrogen Bond Acceptors:	1
logP:	1.43
Molar Refractivity:	36.21
Fraction sp3 Carbons:	0.12
sp3 Carbons:	1

Human Pathway links:

REACTOME pathways containing this metabolite

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", 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, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y