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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:23:27 UTC

Update Date

2021-09-26 22:55:24 UTC

HMDB ID

HMDB0246365

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4-Aminothiophenol

Description

4-Aminothiophenol, also known as 6976-04-1 (na salt) or p-mercaptoaniline, belongs to the class of organic compounds known as thiophenols. Thiophenols are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom. Based on a literature review a significant number of articles have been published on 4-Aminothiophenol. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-aminothiophenol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-Aminothiophenol 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
6976-04-1 (Na salt)	HMDB
p-Aminothiophenol	HMDB
p-Mercaptoaniline	HMDB

Chemical Formula

C₆H₇NS

Average Molecular Weight

125.19

Monoisotopic Molecular Weight

125.029920403

IUPAC Name

4-aminobenzene-1-thiol

Traditional Name

4-aminobenzenethiol

CAS Registry Number

Not Available

SMILES

NC1=CC=C(S)C=C1

InChI Identifier

InChI=1S/C6H7NS/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2

InChI Key

WCDSVWRUXWCYFN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as thiophenols. Thiophenols are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Thiophenols

Sub Class

Not Available

Direct Parent

Thiophenols

Alternative Parents

Substituents

Aniline or substituted anilines
Thiophenol
Monocyclic benzene moiety
Arylthiol
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Primary amine
Organosulfur 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)

Source

Exogenous

Exogenous (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	1.57	ALOGPS
logP	1.24	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	6.86	ChemAxon
pKa (Strongest Basic)	4.82	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	26.02 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	38.77 m³·mol⁻¹	ChemAxon
Polarizability	13.4 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]+	126.213	30932474
DeepCCS	[M-H]-	122.773	30932474
DeepCCS	[M-2H]-	159.631	30932474
DeepCCS	[M+Na]+	134.81	30932474
AllCCS	[M+H]+	125.5	32859911
AllCCS	[M+H-H2O]+	120.6	32859911
AllCCS	[M+NH4]+	129.9	32859911
AllCCS	[M+Na]+	131.2	32859911
AllCCS	[M-H]-	122.9	32859911
AllCCS	[M+Na-2H]-	125.5	32859911
AllCCS	[M+HCOO]-	128.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4-Aminothiophenol	NC1=CC=C(S)C=C1	2472.2	Standard polar	33892256
4-Aminothiophenol	NC1=CC=C(S)C=C1	1297.6	Standard non polar	33892256
4-Aminothiophenol	NC1=CC=C(S)C=C1	1321.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4-Aminothiophenol,1TMS,isomer #1	C[Si](C)(C)SC1=CC=C(N)C=C1	1547.8	Semi standard non polar	33892256
4-Aminothiophenol,1TMS,isomer #1	C[Si](C)(C)SC1=CC=C(N)C=C1	1537.8	Standard non polar	33892256
4-Aminothiophenol,1TMS,isomer #1	C[Si](C)(C)SC1=CC=C(N)C=C1	2026.1	Standard polar	33892256
4-Aminothiophenol,1TMS,isomer #2	C[Si](C)(C)NC1=CC=C(S)C=C1	1643.9	Semi standard non polar	33892256
4-Aminothiophenol,1TMS,isomer #2	C[Si](C)(C)NC1=CC=C(S)C=C1	1553.0	Standard non polar	33892256
4-Aminothiophenol,1TMS,isomer #2	C[Si](C)(C)NC1=CC=C(S)C=C1	1640.8	Standard polar	33892256
4-Aminothiophenol,2TMS,isomer #1	C[Si](C)(C)NC1=CC=C(S[Si](C)(C)C)C=C1	1743.7	Semi standard non polar	33892256
4-Aminothiophenol,2TMS,isomer #1	C[Si](C)(C)NC1=CC=C(S[Si](C)(C)C)C=C1	1645.6	Standard non polar	33892256
4-Aminothiophenol,2TMS,isomer #1	C[Si](C)(C)NC1=CC=C(S[Si](C)(C)C)C=C1	1657.7	Standard polar	33892256
4-Aminothiophenol,2TMS,isomer #2	C[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C	1674.9	Semi standard non polar	33892256
4-Aminothiophenol,2TMS,isomer #2	C[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C	1698.4	Standard non polar	33892256
4-Aminothiophenol,2TMS,isomer #2	C[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C	1651.5	Standard polar	33892256
4-Aminothiophenol,3TMS,isomer #1	C[Si](C)(C)SC1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1	1763.9	Semi standard non polar	33892256
4-Aminothiophenol,3TMS,isomer #1	C[Si](C)(C)SC1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1	1755.8	Standard non polar	33892256
4-Aminothiophenol,3TMS,isomer #1	C[Si](C)(C)SC1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1	1611.4	Standard polar	33892256
4-Aminothiophenol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)SC1=CC=C(N)C=C1	1782.4	Semi standard non polar	33892256
4-Aminothiophenol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)SC1=CC=C(N)C=C1	1763.7	Standard non polar	33892256
4-Aminothiophenol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)SC1=CC=C(N)C=C1	2156.0	Standard polar	33892256
4-Aminothiophenol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=CC=C(S)C=C1	1837.5	Semi standard non polar	33892256
4-Aminothiophenol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=CC=C(S)C=C1	1754.8	Standard non polar	33892256
4-Aminothiophenol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=CC=C(S)C=C1	1799.1	Standard polar	33892256
4-Aminothiophenol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=CC=C(S[Si](C)(C)C(C)(C)C)C=C1	2255.5	Semi standard non polar	33892256
4-Aminothiophenol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=CC=C(S[Si](C)(C)C(C)(C)C)C=C1	2076.3	Standard non polar	33892256
4-Aminothiophenol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=CC=C(S[Si](C)(C)C(C)(C)C)C=C1	1951.0	Standard polar	33892256
4-Aminothiophenol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C(C)(C)C	2082.1	Semi standard non polar	33892256
4-Aminothiophenol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C(C)(C)C	2121.7	Standard non polar	33892256
4-Aminothiophenol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C(C)(C)C	1880.2	Standard polar	33892256
4-Aminothiophenol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)SC1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	2468.7	Semi standard non polar	33892256
4-Aminothiophenol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)SC1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	2342.0	Standard non polar	33892256
4-Aminothiophenol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)SC1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	2017.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4-Aminothiophenol GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-8900000000-adbcfaebcaf51234928a	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-Aminothiophenol 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 - 4-Aminothiophenol 10V, Positive-QTOF	splash10-004i-0900000000-982c1029cfb7ba6c6d73	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Aminothiophenol 20V, Positive-QTOF	splash10-004i-1900000000-e7d08716dbe5d1058011	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Aminothiophenol 40V, Positive-QTOF	splash10-0159-9000000000-e1c2e07562715e7c0804	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Aminothiophenol 10V, Negative-QTOF	splash10-00di-0900000000-0b3c38cc956ef5ade379	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Aminothiophenol 20V, Negative-QTOF	splash10-00di-0900000000-0b3c38cc956ef5ade379	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Aminothiophenol 40V, Negative-QTOF	splash10-0ab9-9300000000-e2420bc4834274553d5e	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
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, 100 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	¹³C 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	¹H NMR Spectrum (1D, 400 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	¹³C NMR Spectrum (1D, 500 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, 600 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, 700 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, 800 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, 900 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

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

13854

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Aminothiophenol

METLIN ID

Not Available

PubChem Compound

14510

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 4-Aminothiophenol (HMDB0246365)

MOL for HMDB0246365 (4-Aminothiophenol)

3D MOL for HMDB0246365 (4-Aminothiophenol)

3D SDF for HMDB0246365 (4-Aminothiophenol)

3D-SDF for HMDB0246365 (4-Aminothiophenol)

PDB for HMDB0246365 (4-Aminothiophenol)

3D PDB for HMDB0246365 (4-Aminothiophenol)

SMILES for HMDB0246365 (4-Aminothiophenol)

INCHI for HMDB0246365 (4-Aminothiophenol)

Structure for HMDB0246365 (4-Aminothiophenol)

3D Structure for HMDB0246365 (4-Aminothiophenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra