Results for:
chemical Classification: Pyrazoles

1,3,5-trimethylpyrazole

Compound Details

Synonymous names

1,3,5-TRIMETHYLPYRAZOLE

1072-91-9

1,3,5-Trimethyl-1H-pyrazole

1H-Pyrazole, 1,3,5-trimethyl-

Pyrazole, 1,3,5-trimethyl-

63938V7Z82

UNII-63938V7Z82

SCHEMBL147208

DTXSID70147951

1,3,5-Trimethylpyrazole, 97%

CHEBI:195104

HNOQAFMOBRWDKQ-UHFFFAOYSA-N

1,3,5-Trimethyl-1H-pyrazole #

BCP18636

HY-N7086

MFCD00015536

s5147

STK396612

AKOS002656998

AC-4834

CCG-266050

CS-W013666

DS-1495

MCULE-1448165985

PD088276

DB-027318

T2724

EN300-35528

11B-132

Q-101972

Q27263586

Microorganism:

Yes

IUPAC name

1,3,5-trimethylpyrazole

SMILES

CC1=CC(=NN1C)C

Inchi

InChI=1S/C6H10N2/c1-5-4-6(2)8(3)7-5/h4H,1-3H3

Formula

C₆H₁₀N₂

PubChem ID

14081

Molweight

110.16

LogP

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds pyrazoles nitrogen compounds heterocyclic compounds

CHEBI-ID

195104

mVOC Specific Details

Massbank-Links

Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP000469

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Saccharomyces Cerevisiae	NA	NA	Harris et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Saccharomyces Cerevisiae	malt extract broth	HS-SPME with GC-MS	no

N-methyl-2-(1-methylpyrazol-4-yl)ethanamine

Compound Details

Synonymous names

N-Methyl-2-(1-methyl-1H-pyrazol-4-yl)ethanamine

1093879-63-0

N-methyl-2-(1-methylpyrazol-4-yl)ethanamine

N-Methyl-2-(1-methyl-1H-pyrazol-4-yl)ethan-1-amine

methyl[2-(1-methylpyrazol-4-yl)ethyl]amine

methyl[2-(1-methyl-1H-pyrazol-4-yl)ethyl]amine

SCHEMBL3509780

DTXSID90679567

AMY21330

MFCD16556159

AKOS005174356

AT27263

MCULE-8294222869

DA-15664

LS-04469

CS-0301715

EN300-1231548

N-methyl-2-(1-methyl-1H-pyrazol-4-yl)ethanamine(SALTDATA: FREE)

Microorganism:

Yes

IUPAC name

N-methyl-2-(1-methylpyrazol-4-yl)ethanamine

SMILES

CNCCC1=CN(N=C1)C

Inchi

InChI=1S/C7H13N3/c1-8-4-3-7-5-9-10(2)6-7/h5-6,8H,3-4H2,1-2H3

Formula

C₇H₁₃N₃

PubChem ID

51000371

Molweight

139.2

LogP

0.1

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

pyrazoles aromatic compounds nitrogen compounds amines heterocyclic compounds

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Saccharomyces Cerevisiae	NA	NA	Harris et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Saccharomyces Cerevisiae	malt extract broth	HS-SPME with GC-MS	no

5-methyl-1H-pyrazole

Mass-Spectra

Compound Details

Synonymous names

3-Methylpyrazole

5-methyl-1H-pyrazole

1453-58-3

3-Methyl-1H-pyrazole

88054-14-2

1H-Pyrazole,5-methyl-

1H-Pyrazole, 3-methyl-

5-Methylpyrazole

3(5)-Methylpyrazole

1H-Pyrazole, 5-methyl-

Pyrazole, 5-methyl-

PYRAZOLE, 3-METHYL-

methylpyrazole

3-Methyl pyrazole

1H-pyrazole-3-methyl

MFCD00005240

MFCD08685900

W7KU1RRO6U

CHEMBL3275944

EINECS 215-925-7

UNII-W7KU1RRO6U

BRN 0001454

3-methyl-pyrazole

3-methyl-1-H-pyrazole

3-Methyl-1,2-diazole

3-Methylpyrazole, 97%

EC 215-925-7

3-methyl-1(2)H-pyrazole

5-23-05-00004 (Beilstein Handbook Reference)

Pyrazole, 3(or 5)-methyl-

DTXSID3073260

5-Methyl-1H-pyrazole, AldrichCPR

BCP23867

CS-B0947

STR06996

BDBM50497139

s5146

STK263690

AKOS000265788

AKOS000311487

AC-2646

AM62623

CCG-266014

FD18008

MCULE-3441401586

HY-66054

PD088278

DB-028555

AM20120265

M0564

NS00001409

EN300-44939

3-Methylpyrazole, analytical reference material

J-512822

Q-101885

Q27292441

F9995-1460

Z450469310

Pyrazole, 3(or 5)-methyl- (6CI,7CI); Pyrazole, 3-methyl- (8CI); 3-Methyl-1H-pyrazole; 3-Methylpyrazole; 5-Methylpyrazole

Microorganism:

Yes

IUPAC name

5-methyl-1H-pyrazole

SMILES

CC1=CC=NN1

Inchi

InChI=1S/C4H6N2/c1-4-2-3-5-6-4/h2-3H,1H3,(H,5,6)

Formula

C₄H₆N₂

PubChem ID

15073

Molweight

82.1

LogP

0.6

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds nitrogen compounds pyrazoles heterocyclic compounds

Supernatural-ID

SN0432930

mVOC Specific Details

Massbank-Links

Massbank Spectrum MSBNK-CASMI_2016-SM804001

Massbank Spectrum MSBNK-CASMI_2016-SM804101

Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP000454

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Tuber Melanosporum	n/a	Agricultural Centre of Castilla and LeÃƒÂ³n Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).	Diaz et al. 2003
Prokaryota	Streptomyces Thermocarboxydus	NA	NA	Passari et al. 2019

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Tuber Melanosporum	n/a	n/a	no
Prokaryota	Streptomyces Thermocarboxydus	actinomycetes isolation agar (AIA)	GC-MS	no

3,4,5-trimethyl-1H-pyrazole

Mass-Spectra

Compound Details

Synonymous names

3,4,5-Trimethyl-1H-pyrazole

5519-42-6

3,4,5-Trimethylpyrazole

1H-Pyrazole, 3,4,5-trimethyl-

U620SU1FNR

CHEMBL4514142

MFCD00040246

UNII-U620SU1FNR

ENDOSULFANALCOHOL

SCHEMBL12415

F3379-0319

DTXSID70203687

3,4,5-Trimethyl-1H-pyrazole #

BDBM50591486

STK396608

AKOS000276353

MCULE-7986153155

NCGC00341494-01

LS-01689

SY173857

3,4,5-Trimethyl-1H-pyrazole, AldrichCPR

DB-081744

EN300-53144

E85593

AB01333398-02

Q27290730

Z50145985

Microorganism:

IUPAC name

3,4,5-trimethyl-1H-pyrazole

SMILES

CC1=C(NN=C1C)C

Inchi

InChI=1S/C6H10N2/c1-4-5(2)7-8-6(4)3/h1-3H3,(H,7,8)

Formula

C₆H₁₀N₂

PubChem ID

138528

Molweight

110.16

LogP

1.4

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds nitrogen compounds pyrazoles heterocyclic compounds

mVOC Specific Details

Massbank-Links

Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP000470

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Pleurotus Cystidiosus	na	na	Usami et al. 2014

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Pleurotus Cystidiosus	na	GC/MS, GC-O, AEDA	no

1,3,5-trimethylpyrazol-4-amine

Compound Details

Synonymous names

1,3,5-Trimethyl-1H-pyrazol-4-amine

28466-21-9

4-Amino-1,3,5-trimethylpyrazole

1,3,5-trimethylpyrazol-4-amine

4-Amino-1,3,5-trimethyl-1H-pyrazole

1H-Pyrazol-4-amine, 1,3,5-trimethyl-

Pyrazole, 4-amino-1,3,5-trimethyl-

trimethyl-1H-pyrazol-4-amine

MFCD00052883

1,3,5-trimethyl-1H-pyrazol-4-ylamine

BRN 0110739

trimethylpyrazol-4-amine

1,3,5-trimethyl-1H-pyrazole-4-amine

SCHEMBL1559796

DTXSID70182680

TQP0942

CHEBI:195137

4-amino-1 ,3,5-trimethylpyrazole

BBL012617

STK347833

AKOS000104444

CS-W011170

MCULE-3122375399

PS-6028

4-amino-2,3,5-trimethyl-2H-pyrazole

SY122576

EN300-11797

A876713

AN-989/25109004

J-503846

Z57980325

F2124-0253

Microorganism:

Yes

IUPAC name

1,3,5-trimethylpyrazol-4-amine

SMILES

CC1=C(C(=NN1C)C)N

Inchi

InChI=1S/C6H11N3/c1-4-6(7)5(2)9(3)8-4/h7H2,1-3H3

Formula

C₆H₁₁N₃

PubChem ID

161603

Molweight

125.17

LogP

0.4

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds amines pyrazoles nitrogen compounds

CHEBI-ID

195137

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Saccharomyces Cerevisiae	NA	NA	Harris et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Saccharomyces Cerevisiae	malt extract broth	HS-SPME with GC-MS	no

1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone

Compound Details

Synonymous names

1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone

1123-48-4

4-acetyl-3,5-dimethylpyrazole

1-(3,5-dimethyl-1H-pyrazol-4-yl)ethan-1-one

NSC45012

1-(3,5-Dimethyl-1H-pyrazol-4-yl)-ethanone

SCHEMBL1640767

DTXSID50286352

MFCD00234353

NSC-45012

STK070224

AKOS002665027

MCULE-4549522309

NCGC00325046-01

AM802939

AS-39439

DB-013759

CS-0313087

AB01322236-02

Microorganism:

Yes

IUPAC name

1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone

SMILES

CC1=C(C(=NN1)C)C(=O)C

Inchi

InChI=1S/C7H10N2O/c1-4-7(6(3)10)5(2)9-8-4/h1-3H3,(H,8,9)

Formula

C₇H₁₀N₂O

PubChem ID

239664

Molweight

138.17

LogP

0.7

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic ketones nitrogen compounds heterocyclic compounds pyrazoles aromatic compounds ketones

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Saccharomyces Cerevisiae	NA	NA	Harris et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Saccharomyces Cerevisiae	malt extract broth	HS-SPME with GC-MS	no

1H-pyrazol-4-ylmethanol

Compound Details

Synonymous names

(1H-PYRAZOL-4-YL)METHANOL

25222-43-9

1H-Pyrazole-4-methanol

1H-pyrazol-4-ylmethanol

4-hydroxymethylpyrazole

4-(HYDROXYMETHYL)PYRAZOLE

MFCD06797673

5Z3Y85WYBN

4-Hydroxymethyl-1H-pyrazole

CHEMBL3276272

UNII-5Z3Y85WYBN

pyrazole-4-methanol

(1H-Pyrazol-4-yl)methano

(1H-pyrazol-4-yl)-methanol

AMY5501

DTXSID60179882

CHEBI:179583

JRMKJOOJKCAEJK-UHFFFAOYSA-N

4-HYROXYMETHYL-1H-PYRAZOLE

BDBM50497138

STL415033

AKOS005169571

CS-W009163

GS-4530

MCULE-3322868006

PB34185

(1H-pyrazol-4-yl)methanol, AldrichCPR

AC-31827

HY-33914

PD157939

SY042536

DB-067353

EN300-54500

A817718

1H-pyrazol-4-ylmethanol;(1H-Pyrazol-4-yl)methanol

J-500196

J-524077

Q27263083

(1H-Pyrazol-4-yl)Methanol;4-Hydroxymethyl-1h-pyrazole

Z812520032

Microorganism:

Yes

IUPAC name

1H-pyrazol-4-ylmethanol

SMILES

C1=C(C=NN1)CO

Inchi

InChI=1S/C4H6N2O/c7-3-4-1-5-6-2-4/h1-2,7H,3H2,(H,5,6)

Formula

C₄H₆N₂O

PubChem ID

3015210

Molweight

98.1

LogP

0.2

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic alcohols alcohols nitrogen compounds pyrazoles heterocyclic compounds

CHEBI-ID

179583

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Prokaryota	Streptococcus Pneumoniae	NA	NA	Kaeslin et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Prokaryota	Streptococcus Pneumoniae	BHI	SESI-MS	no

4-bromo-1H-pyrazole

Compound Details

Synonymous names

4-Bromo-1H-pyrazole

4-Bromopyrazole

2075-45-8

1H-Pyrazole, 4-bromo-

PYRAZOLE, 4-BROMO-

4-Brompyrazole

4-bromo-pyrazole

MFCD00075602

NSC-522023

4-Bromopyrazole; NSC 522023

NSC 522023

BRN 0106510

4-bromo pyrazole

BYZ

JCB5VB9RTA

4-Bromo-1-H-pyrazole

4-Bromopyrazole, 99%

WLN: T5MNJ DE

SCHEMBL10169

5-23-04-00172 (Beilstein Handbook Reference)

CHEMBL4440111

DTXSID50174826

ALBB-000287

AMY12221

NSC522023

STK301300

AKOS000304500

AB02892

AC-2709

AS-5543

CS-W009265

BP-21496

HY-78243

SY002635

DB-262940

A4505

AM20090168

B3745

EN300-50991

AC-907/25014004

J-013590

Q27458577

F0001-0740

Z275169750

Microorganism:

IUPAC name

4-bromo-1H-pyrazole

SMILES

C1=C(C=NN1)Br

Inchi

InChI=1S/C3H3BrN2/c4-3-1-5-6-2-3/h1-2H,(H,5,6)

Formula

C₃H₃BrN₂

PubChem ID

16375

Molweight

146.97

LogP

0.3

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

pyrazoles nitrogen compounds heterocyclic compounds halogenated compounds bromides

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Flavus			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Flavus	inoculated potato samples	GC-MS	no

[2,3-diacetyloxy-3-(1-phenylpyrazolo[4,3-b]quinoxalin-3-yl)propyl] Acetate

Compound Details

Synonymous names

NSC713358

HDNQAKKTCNJTOK-UHFFFAOYSA-N

NSC-713358

1,2,3-Propanetriol, 1-(1-phenyl-1H-pyrazolo[3,4-b]quinoxalin-3-yl)-, triacetate (ester), [S-(R*,S*)]-

2-(Acetyloxy)-1-[(acetyloxy)methyl]-2-(1-phenyl-1H-pyrazolo[3,4-b]quinoxalin-3-yl)ethyl acetate #

Microorganism:

IUPAC name

[2,3-diacetyloxy-3-(1-phenylpyrazolo[4,3-b]quinoxalin-3-yl)propyl] acetate

SMILES

CC(=O)OCC(C(C1=NN(C2=NC3=CC=CC=C3N=C12)C4=CC=CC=C4)OC(=O)C)OC(=O)C

Inchi

InChI=1S/C24H22N4O6/c1-14(29)32-13-20(33-15(2)30)23(34-16(3)31)21-22-24(26-19-12-8-7-11-18(19)25-22)28(27-21)17-9-5-4-6-10-17/h4-12,20,23H,13H2,1-3H3

Formula

C₂₄H₂₂N₄O₆

PubChem ID

400838

Molweight

462.5

LogP

2.5

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds benzenoids esters nitrogen compounds pyrazoles quinoxalines

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Niger			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Niger	inoculated potato samples	GC-MS	no

3,3-dimethyl-4-(methylamino)butan-2-one

Compound Details

Synonymous names

3,3-dimethyl-4-(methylamino)butan-2-one

3,3-Dimethyl-4-methylamino-butan-2-one

123528-99-4

2-Butanone, 3,3-dimethyl-4-(methylamino)- (9CI)

SCHEMBL12798153

QPKSAEVZZQMSER-UHFFFAOYSA-N

AKOS006353915

DB-281219

3,3-Dimethyl-4-(methylamino)-2-butanone #

2-BUTANONE, 3,3-DIMETHYL-4-(METHYLAMINO)-

Microorganism:

Yes

IUPAC name

3,3-dimethyl-4-(methylamino)butan-2-one

SMILES

CC(=O)C(C)(C)CNC

Inchi

InChI=1S/C7H15NO/c1-6(9)7(2,3)5-8-4/h8H,5H2,1-4H3

Formula

C₇H₁₅NO

PubChem ID

541550

Molweight

129.2

LogP

0.4

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

amines dioxanes esters heterocyclic compounds nitrogen compounds pyrazoles

Supernatural-ID

SN0311650

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Fusarium Graminearum			Ballot et al. 2023
	Microbacterium			Ballot et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Fusarium Graminearum	tryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)	GC-QQQ-MS	no
	Microbacterium	tryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)	GC-QQQ-MS	no

1-(9-borabicyclo[3.3.1]nonan-9-yl)-3,5-ditert-butylpyrazole

Compound Details

Synonymous names

SZXOLJDCCBPVMW-UHFFFAOYSA-N

1-(9-Borabicyclo[3.3.1]non-9-yl)-3,5-ditert-butyl-1H-pyrazole #

1H-Pyrazole, 1-(9-borabicyclo[3.3.1]non-9-yl)-3,5-bis(1,1-dimethylethyl)-

Microorganism:

Yes

IUPAC name

1-(9-borabicyclo[3.3.1]nonan-9-yl)-3,5-ditert-butylpyrazole

SMILES

B1(C2CCCC1CCC2)N3C(=CC(=N3)C(C)(C)C)C(C)(C)C

Inchi

InChI=1S/C19H33BN2/c1-18(2,3)16-13-17(19(4,5)6)22(21-16)20-14-9-7-10-15(20)12-8-11-14/h13-15H,7-12H2,1-6H3

Formula

C₁₉H₃₃BN₂

PubChem ID

618108

Molweight

300.3

LogP

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

aromatic compounds boron compounds heterocyclic compounds nitrogen compounds pyrazoles

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Pectobacterium Carotovorum			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Pectobacterium Carotovorum	inoculated potato samples	GC-MS	no

Ethyl 5-amino-1-(4,7-dimethyl-1,3-benzothiazol-2-yl)pyrazole-4-carboxylate

Compound Details

Synonymous names

SBVHLGGGRMBIPT-UHFFFAOYSA-N

STL162718

AKOS005762390

ethyl 5-amino-1-(4,7-dimethyl-1,3-benzothiazol-2-yl)-1H-pyrazole-4-carboxylate

ethyl 5-amino-1-(4,7-dimethyl-1,3-benzothiazol-2-yl)pyrazole-4-carboxylate

Microorganism:

IUPAC name

ethyl 5-amino-1-(4,7-dimethyl-1,3-benzothiazol-2-yl)pyrazole-4-carboxylate

SMILES

CCOC(=O)C1=C(N(N=C1)C2=NC3=C(C=CC(=C3S2)C)C)N

Inchi

InChI=1S/C15H16N4O2S/c1-4-21-14(20)10-7-17-19(13(10)16)15-18-11-8(2)5-6-9(3)12(11)22-15/h5-7H,4,16H2,1-3H3

Formula

C₁₅H₁₆N₄O₂S

PubChem ID

51054232

Molweight

316.4

LogP

3.8

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

amines aromatic compounds benzenoids esters heterocyclic compounds nitrogen compounds pyrazoles sulfur compounds thiazoles

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Flavus			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Flavus	inoculated potato samples	GC-MS	no

N-methyl-N-[4-[(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)amino]phenyl]acetamide

Compound Details

Synonymous names

VYIALUFCLZTALA-CZIZESTLSA-N

acetamide, N-[4-[[1,5-dihydro-3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylidene]amino]phenyl]-N-methyl-

Microorganism:

IUPAC name

N-methyl-N-[4-[(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)amino]phenyl]acetamide

SMILES

CC1=NN(C(=O)C1=NC2=CC=C(C=C2)N(C)C(=O)C)C3=CC=CC=C3

Inchi

InChI=1S/C19H18N4O2/c1-13-18(19(25)23(21-13)17-7-5-4-6-8-17)20-15-9-11-16(12-10-15)22(3)14(2)24/h4-12H,1-3H3

Formula

C₁₉H₁₈N₄O₂

PubChem ID

91743027

Molweight

334.4

LogP

2.3

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

amides aromatic compounds benzenoids heterocyclic compounds imines pyrazoles

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
	Aspergillus Niger			Kate et al. 2023

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
	Aspergillus Niger	inoculated potato samples	GC-MS	no

Results for: chemical Classification: Pyrazoles

1,3,5-trimethylpyrazole

Compound Details

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N-methyl-2-(1-methylpyrazol-4-yl)ethanamine

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5-methyl-1H-pyrazole

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3,4,5-trimethyl-1H-pyrazole

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1,3,5-trimethylpyrazol-4-amine

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1-(3,5-dimethyl-1H-pyrazol-4-yl)ethanone

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1H-pyrazol-4-ylmethanol

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4-bromo-1H-pyrazole

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[2,3-diacetyloxy-3-(1-phenylpyrazolo[4,3-b]quinoxalin-3-yl)propyl] Acetate

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3,3-dimethyl-4-(methylamino)butan-2-one

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1-(9-borabicyclo[3.3.1]nonan-9-yl)-3,5-ditert-butylpyrazole

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Ethyl 5-amino-1-(4,7-dimethyl-1,3-benzothiazol-2-yl)pyrazole-4-carboxylate

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N-methyl-N-[4-[(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)amino]phenyl]acetamide

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Results for:
chemical Classification: Pyrazoles