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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 01:36:23 UTC

Update Date

2021-09-26 22:58:33 UTC

HMDB ID

HMDB0248329

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Aminophenetole

Description

1-phenoxyethan-1-amine belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. Based on a literature review very few articles have been published on 1-phenoxyethan-1-amine. This compound has been identified in human blood as reported by (PMID: 31557052 ). Aminophenetole is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Aminophenetole is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Phenetidine	MeSH
Ethoxyaniline	MeSH

Chemical Formula

C₈H₁₁NO

Average Molecular Weight

137.182

Monoisotopic Molecular Weight

137.084063978

IUPAC Name

1-phenoxyethan-1-amine

Traditional Name

1-phenoxyethanamine

CAS Registry Number

Not Available

SMILES

CC(N)OC1=CC=CC=C1

InChI Identifier

InChI=1S/C8H11NO/c1-7(9)10-8-5-3-2-4-6-8/h2-7H,9H2,1H3

InChI Key

QYYKZVMRNIHICX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenol ethers

Sub Class

Not Available

Direct Parent

Phenol ethers

Alternative Parents

Substituents

Phenoxy compound
Phenol ether
Monocyclic benzene moiety
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Amine
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	0.97	ALOGPS
logP	1.36	ChemAxon
logS	-0.93	ALOGPS
pKa (Strongest Basic)	8.26	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	35.25 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	40.12 m³·mol⁻¹	ChemAxon
Polarizability	15.16 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	130.036	30932474
DeepCCS	[M-H]-	126.667	30932474
DeepCCS	[M-2H]-	163.865	30932474
DeepCCS	[M+Na]+	139.032	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Aminophenetole	CC(N)OC1=CC=CC=C1	1729.2	Standard polar	33892256
Aminophenetole	CC(N)OC1=CC=CC=C1	1121.5	Standard non polar	33892256
Aminophenetole	CC(N)OC1=CC=CC=C1	1137.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Aminophenetole,1TMS,isomer #1	CC(N[Si](C)(C)C)OC1=CC=CC=C1	1280.7	Semi standard non polar	33892256
Aminophenetole,1TMS,isomer #1	CC(N[Si](C)(C)C)OC1=CC=CC=C1	1318.3	Standard non polar	33892256
Aminophenetole,1TMS,isomer #1	CC(N[Si](C)(C)C)OC1=CC=CC=C1	1649.7	Standard polar	33892256
Aminophenetole,2TMS,isomer #1	CC(OC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C	1510.4	Semi standard non polar	33892256
Aminophenetole,2TMS,isomer #1	CC(OC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C	1489.8	Standard non polar	33892256
Aminophenetole,2TMS,isomer #1	CC(OC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C	1697.4	Standard polar	33892256
Aminophenetole,1TBDMS,isomer #1	CC(N[Si](C)(C)C(C)(C)C)OC1=CC=CC=C1	1515.3	Semi standard non polar	33892256
Aminophenetole,1TBDMS,isomer #1	CC(N[Si](C)(C)C(C)(C)C)OC1=CC=CC=C1	1513.9	Standard non polar	33892256
Aminophenetole,1TBDMS,isomer #1	CC(N[Si](C)(C)C(C)(C)C)OC1=CC=CC=C1	1814.1	Standard polar	33892256
Aminophenetole,2TBDMS,isomer #1	CC(OC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	1939.8	Semi standard non polar	33892256
Aminophenetole,2TBDMS,isomer #1	CC(OC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	1889.4	Standard non polar	33892256
Aminophenetole,2TBDMS,isomer #1	CC(OC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	1934.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Aminophenetole GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9100000000-7f51d7c9d309ab28f63d	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Aminophenetole GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Aminophenetole 10V, Positive-QTOF	splash10-000i-2900000000-922483aac7992f8a32ff	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Aminophenetole 20V, Positive-QTOF	splash10-0005-9200000000-e8fb3867be1b569b1b77	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Aminophenetole 40V, Positive-QTOF	splash10-004l-9000000000-1bf270cf546f13ef7093	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Aminophenetole 10V, Negative-QTOF	splash10-0006-9000000000-08485aaf085c13d5129a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Aminophenetole 20V, Negative-QTOF	splash10-0006-9000000000-b8f7ffaa05f86c34a1cf	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Aminophenetole 40V, Negative-QTOF	splash10-0006-9000000000-08485aaf085c13d5129a	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

11184853

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

19808190

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Aminophenetole (HMDB0248329)

MOL for HMDB0248329 (Aminophenetole)

3D MOL for HMDB0248329 (Aminophenetole)

3D SDF for HMDB0248329 (Aminophenetole)

3D-SDF for HMDB0248329 (Aminophenetole)

PDB for HMDB0248329 (Aminophenetole)

3D PDB for HMDB0248329 (Aminophenetole)

SMILES for HMDB0248329 (Aminophenetole)

INCHI for HMDB0248329 (Aminophenetole)

Structure for HMDB0248329 (Aminophenetole)

3D Structure for HMDB0248329 (Aminophenetole)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra