Results for:
chemical Classification: anhydrides

Tert-butyl (2-methylpropan-2-yl)oxycarbonyl Carbonate

Compound Details

Synonymous names

Di-tert-butyl dicarbonate

24424-99-5

BOC anhydride

Bis(tert-butoxycarbonyl)oxide

di-tert-Butyl pyrocarbonate

Di-tert-butyldicarbonate

Boc2O

tert-Butoxycarbonyl anhydride

BOC-anhydride

di-t-Butyl dicarbonate

Dicarbonic acid, bis(1,1-dimethylethyl) ester

Di-t-butyl pyrocarbonate

(boc)2o

tert-Butyl dicarbonate

Pyrocarbonic acid di-tert-butyl ester

di-tert butyl dicarbonate

di-t-butyldicarbonate

di-t-butyl-dicarbonate

ditert-butyldicarbonate

tert-butyl (2-methylpropan-2-yl)oxycarbonyl carbonate

di-tert-butyl-dicarbonate

MFCD00008805

tert-butoxycarbonyl tert-butyl carbonate

Z10Q236C3G

Di-tert-butyl dicarbonate 2.0M in THF

Di-tert-butyl dicarbote

Di-tert-butyl dicarbonate 2.0M in Dichloromethane

Diboc

CCRIS 2598

ditertbutyl dicarbonate

EINECS 246-240-1

di-tert-butyl oxydiformate

UNII-Z10Q236C3G

tBoc2O

Di-tert-butyl dicarbonate (DIBOC)

diterbutyldicarbonate

ditertbutyldicarbonate

di t-butyldicarbonate

di-t butyldicarbonate

diterbutyl dicarbonate

diterbutyl-dicarbonate

t-Boc2O

Di-t-butyidicarbonate

di-tertbutyldicarbonate

ditert butyldicarbonate

ditertbutyl-dicarbonate

di t butyl dicarbonate

di t-butyl dicarbonate

di(t-butyl)dicarbonate

di-t -butyldicarbonate

di-t butyl dicarbonate

di-t butyl-dicarbonate

di-t-butylpyrocarbonate

di-ter-butyldicarbonate

di-terbutyl dicarbonate

di-tert-butydicarbonate

di-tert-butyldicarbonat

(tBoc)2O

Di-tert-buyldicarbonate

di tert butyldicarbonate

di tert-butyldicarbonate

di tert.butyldicarbonate

di-tert butyldicarbonate

di-tert-butyidicarbonate

di-tert.butyldicarbonate

di-tertbutyl dicarbonate

di-tertbutyl-dicarbonate

ditert-butyl dicarbonate

ditert-butyl-dicarbonate

ditert.butyl dicarbonate

Di-tert-butlydicarbonate

di-tertbutylpyrocarbonate

Ditert butyl dicarbonate

di(t-butyl) dicarbonate

di-(t-butyl)dicarbonate

di-ter-butyl dicarbonate

di-ter-butyl-dicarbonate

di-tert-butyl dicabonate

di-tert-butyl dicarbonat

di-tert-butyl-dicarbonat

di-tert.-butyldicarbonat

di-tert.butyl-dicarbonat

tert-butyl (tert-butoxycarbonyloxy)formate

Di-tert-buty dicarbonate

bis(t-butyl)pyrocarbonate

di tert butyl dicarbonate

di tert.-butyldicarbonate

di(t-butoxycarbonyl)ether

di(tert-butyl)dicarbonate

di-tert-butly-dicarbonate

di-tert.-butyldicarbonate

di-tert.butyl dicarbonate

di-tert.butyl-dicarbonate

O(Boc)2

(tBuO2C)2O

Di tert-butyl dicarbonate

Di-tert -butyldicarbonate

Di-tert-butyldicarbon-ate

di-tert-butylpyrocarbonate

di-tert.butylpyrocarbonate

di-tertbutyl-pyrocarbonate

(BOC)2O?Boc Anhydride

di-(t-butyl) dicarbonate

di-tertiarybutyldicarbonate

ditertiary butyldicarbonate

ditertiary-butyldicarbonate

ditertiarybutyl dicarbonate

bis(t-butoxycarbonyl)oxide

bis(tert-butyl)dicarbonate

Di-tert.-butyl-dicarbonat

(di-tert-butyl)dicarbonate

di (tert-butyl)dicarbonate

di(tert-butyl) dicarbonate

di(tert-butyl)-dicarbonate

di(tert.butyl) dicarbonate

di-(tert-butyl)dicarbonate

di-tert -butyl dicarbonate

di-tert-butyl di carbonate

di-tert-butyl- dicarbonate

di-tert. butyl dicarbonate

di-tert. butyl-dicarbonate

di-tert.-butyl dicarbonate

di-tert.-butyl-dicarbonate

di(tert-butyl)pyrocarbonate

di-tert-butyl-pyrocarbonate

di-tert.-butylpyrocarbonate

di-tert.butyl pyrocarbonate

ditert.-butyl pyrocarbonate

di-tertiary-butyldicarbonate

di-tertiarybutyl dicarbonate

ditertiary butyl dicarbonate

EC 246-240-1

t-Butoxycarboxylic anhydride

(t-BOC)2O

bis(t-butoxycarbonyl) oxide

bis(tert-butyl) dicarbonate

SCHEMBL5452

di(-tert.butyl) dicarbonate

di-(tert-butyl) dicarbonate

di-tert. butyl pyrocarbonate

di-tert.-butyl pyrocarbonate

di tertiary butyl dicarbonate

di-tertiary butyl dicarbonate

di-tertiary butyl-dicarbonate

di-tertiary-butyl dicarbonate

di-tertiary-butyl-dicarbonate

Di(tertiarybutyl) dicarbonate

di-tert. -butyl pyrocarbonate

tert-butoxycarboxylic anhydride

DTXSID4051904

CHEBI:48500

di(1,1-dimethylethyl)dicarbonate

bis(1,1-dimethylethyl)dicarbonate

dicarbonic acid di(t-butyl) ester

di(1,1-dimethylethyl) dicarbonate

pyrocarbonic acid di-t-butyl ester

Bis(1,1-dimethylethyl)dicarbonoate

BCP26395

bis(1,1'-dimethylethyl)dicarbonate

bis(1,1-dimethylethyl) dicarbonate

Bis(1,1-dimethylethyl)-dicarbonate

pyrocarbonic acid-di-tert-butylester

STR01939

tert-butoxycarboxylic acid anhydride

bis (1,1-dimethylethyl) dicarbonate

Bis(1,1-dimethylethyl) dicarbonoate

pyrocarbonic acid di-tert.butyl ester

pyrocarbonic acid-di-tert-butyl ester

1,1-dimethylethoxycarboxylic anhydride

AKOS000121490

DI-TERT-BUTYL DICARBONATE [MI]

MCULE-1408482476

Di-tert-butyl dicarbonate 1.0M in THF

pyrocarbonic acid ditertiary butyl ester

tert-butyl(tert-butoxycarbonyloxy)formate

BP-20551

Di-tert-butyl pyrocarbonate; Dicarbonic acid bis(1,1-dimethylethyl)ester; Pyrocarbonic acid di-tert-butyl ester

PD118138

AM20090273

CS-0017817

D1547

D3878

D3879

D3880

Di-tert-butyl dicarbonate, >=98.0% (GC)

NS00000554

tert-butyl[(tert-butyl)oxycarbonyloxy]formate

EN300-17516

tert-butyl [(tert-butyl)oxycarbonyloxy]formate

A15406

BOC anhydride;DIBOC;Di-tert-butyl dicarbonate

C90704

Di-tert-butyl dicarbonate 2.0M in Ethyl acetate

Di-tert-butyl dicarbonate, ReagentPlus(R), 99%

carbonic acid tert-butoxycarbonyl tert-butyl ester

Q175718

Di-tert-butyl dicarbonate, ReagentPlus(R), >=99%

Dicarbonic acid, 1,3-bis(1,1-dimethylethyl) ester

J-520400

(2-Methylpropan-2-yl)oxycarbonyl tert-butyl carbonate

F0001-0830

DICARBONIC ACID C,C'-BIS(1,1-DIMETHYLETHYL) ESTER

Microorganism:

Yes

IUPAC name

tert-butyl (2-methylpropan-2-yl)oxycarbonyl carbonate

SMILES

CC(C)(C)OC(=O)OC(=O)OC(C)(C)C

Inchi

InChI=1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3

Formula

C₁₀H₁₈O₅

PubChem ID

90495

Molweight

218.25

LogP

2.7

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

anhydrides carbonates

CHEBI-ID

48500

Supernatural-ID

SN0078747

mVOC Specific Details

Massbank-Links

Massbank Spectrum MSBNK-Eawag-EQ315651

Massbank Spectrum MSBNK-Eawag-EQ315652

Massbank Spectrum MSBNK-Eawag-EQ315653

Massbank Spectrum MSBNK-Eawag-EQ315654

Massbank Spectrum MSBNK-Eawag-EQ315655

Massbank Spectrum MSBNK-Eawag-EQ315656

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Prokaryota	Bacillus Toyonensis	stimulate growth of Solanum tuberosum	isolate from Irish potato soils	Heenan-Daly et al. 2021
Prokaryota	Bacillus Mycoides	stimulate growth of Solanum tuberosum	isolate from Irish potato soils	Heenan-Daly et al. 2021
Prokaryota	Serratia Myotis		isolate from Irish potato soils	Heenan-Daly et al. 2021
Prokaryota	Pseudomonas Azotoformans	stimulate growth of Solanum tuberosum	isolate from Irish potato soils	Heenan-Daly et al. 2021

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Prokaryota	Bacillus Toyonensis	M+S (Murashige and Skoog) media	SPME/GC-MS	no
Prokaryota	Bacillus Mycoides	M+S (Murashige and Skoog) media	SPME/GC-MS	no
Prokaryota	Serratia Myotis	TSB media	SPME/GC-MS	no
Prokaryota	Pseudomonas Azotoformans	M+S (Murashige and Skoog) media	SPME/GC-MS	no

Hexanoyl Hexanoate

Compound Details

Synonymous names

Hexanoic anhydride

2051-49-2

Caproic anhydride

hexanoyl hexanoate

Hexanoic acid, 1,1'-anhydride

Hexanoic acid, anhydride

n-Hexanoic anhydride

HexanoicAnhydride

Caproic acid anhydride

Capronic acid anhydride

n-Hexanoic acid anhydride

Capronic anhydride

Hexanoyl anhydride

hexanoic acid anhydride

GG70Y8LTBY

MFCD00009509

n-Caproic anhydride

UNII-GG70Y8LTBY

EINECS 218-121-4

AI3-06132

Hexanoic anhydride, 97%

?HEXANOIC ANHYDRIDE

EC 218-121-4

hexanoic acid hexanoyl ester

SCHEMBL1783

DTXSID20870929

AKOS015950716

HY-W127410

AS-18084

PERFLUOROCYCLOHEXANECARBONYLCHLORIDE

CS-0185644

Hexanoic anhydride, purum, >=97.0% (GC)

NS00003838

F87206

A814628

J-013374

Q27279092

Microorganism:

Yes

IUPAC name

hexanoyl hexanoate

SMILES

CCCCCC(=O)OC(=O)CCCCC

Inchi

InChI=1S/C12H22O3/c1-3-5-7-9-11(13)15-12(14)10-8-6-4-2/h3-10H2,1-2H3

Formula

C₁₂H₂₂O₃

PubChem ID

74918

Molweight

214.3

LogP

3.7

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

anhydrides

mVOC Specific Details

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Eukaryota	Wickerhamomyces Anomalus	NA	NA	Shi et al. 2022

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Eukaryota	Wickerhamomyces Anomalus	medium consisted of glucose (20 g/l), peptone (5 g/l), agar (20 g/l) and amoxicillin (1 g/l)	SPME with GC-MS	no
Eukaryota	Wickerhamomyces Anomalus	solid-state fermentation starter culture Daqu	SPME coupled with GC-MS	no

3,3-dimethyloxane-2,6-dione

Compound Details

Synonymous names

2,2-Dimethylglutaric anhydride

2938-48-9

3,3-dimethyloxane-2,6-dione

3,3-Dimethyldihydro-2H-pyran-2,6(3H)-dione

2H-Pyran-2,6(3H)-dione, dihydro-3,3-dimethyl-

2WKF1QUU1D

Dihydro-3,3-dimethyl-2H-pyran-2,6(3H)-dione

MFCD00006682

NSC-60199

3,3-dimethyl-dihydro-pyran-2,6-dione

.alpha.,.alpha.-Dimethyl glutaric anhydride

2,2-Dimethylglutaricanhydride

EINECS 220-922-9

3,3-dimethyltetrahydropyran-2,6-dione

UNII-2WKF1QUU1D

SCHEMBL134403

2,2 dimethylglutaric anhydride

2.2-dimethylglutaric anhydride

DTXSID70183612

NSC60199

NSC 60199

2,2-Dimethylglutaric anhydride, 96%

2H-Pyran-2, dihydro-3,3-dimethyl-

AKOS008901072

AS-66598

SY049499

DB-047571

CS-0153793

D1325

NS00028680

D89834

EN300-197423

3,3-Dimethyldihydro-2H-pyran-2,6(3H)-dione #

W-202224

Microorganism:

Yes

IUPAC name

3,3-dimethyloxane-2,6-dione

SMILES

CC1(CCC(=O)OC1=O)C

Inchi

InChI=1S/C7H10O3/c1-7(2)4-3-5(8)10-6(7)9/h3-4H2,1-2H3

Formula

C₇H₁₀O₃

PubChem ID

76247

Molweight

142.15

LogP

0.8

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

anhydrides

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

(1R,2S,6R,7S)-4-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione

Compound Details

Synonymous names

Carbic anhydride

129-64-6

(3aR,4S,7R,7aS)-rel-3a,4,7,7a-Tetrahydro-4,7-methanoisobenzofuran-1,3-dione

Endic anhydride

Himic anhydride

Nadic anhydride

M4UGH0927Z

cis-5-Norbornene-endo-2,3-dicarboxylic anhydride

(1S,2R,6S,7R)-4-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione

(2r,6s)-4-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione

endo-Himic acid anhydride

5-Norbornene-2,3-dicarboxylic anhydride, cis-endo-

8,9,10-Trinorborn-5-ene-2,3-dicarboxylic anhydride

endo-3,6-Methylene-1,2,3,6-tetrahydrophthalic anhydride

Kayahard CD

endo-5-Norbornene-2,3-dicarboxylic anhydride

cis-endo-5-Norbornene-2,3-dicarboxylic anhydride

NSC-3999

NSC 102277

NSC-102277

cis-5-Norbornene-exo-2,3-dicarboxylic anhydride

NADIC ACID ANHYDRIDE

3,6-Endomethylenephthalic anhydride, 1,2,3,6-tetrahydro-

UNII-M4UGH0927Z

CARBIC ANHYDRIDE [MI]

CHEMBL1240586

DTXSID6051647

SCHEMBL10050519

4,7-Methanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aR,4S,7R,7aS)-rel-

KNDQHSIWLOJIGP-UMRXKNAASA-N

EINECS 204-957-7

MFCD00069013

MFCD00151106

AKOS016010258

CS-W010838

FS-3830

E76097

EN300-175579

A805964

endo-cis-5-norbornene-2,3-dicarboxylic anhydride

3,6-Endomethylene-delta4-tetrahydrophthalic anhydride

Q27283494

cis-5-Norbornene-endo-2,3-dicarboxylic anhydride, 99%

ENDO-NORBORNENE-2,3-DICARBOXYLIC ACID ANHYDRIDE

5-NORBORNENE-2,3-DICARBOXYLIC ANHYDRIDE, ENDO-CIS-

bicyclo[2.2.1]hept-2-ene-endo-cis-5,6-dicarboxylic anhydride

cis, Endo-3,6-methylene-1,2,3,6-tetrahydrophthalic anhydride

Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride, >=95.0%

cis-5-Norbornene-endo-2,3-dicarboxylic anhydride, predominantly endo

(1R,2S,6R,7S)-4-oxatricyclo[5.2.1.0,2,6]dec-8-ene-3,5-dione

(1S,2R,6S,7R)-4-Oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dione

4,7-Methanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aalpha,4alpha,7alpha,7aalpha)-

magnesium (4S)-4-[[(2S)-2-acetamido-3-carboxylato-propanoyl]amino]-5-hydroxy-5-oxo-pentanoate;Carbic anhydride

Microorganism:

Yes

IUPAC name

(1R,2S,6R,7S)-4-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione

SMILES

C1C2C=CC1C3C2C(=O)OC3=O

Inchi

InChI=1S/C9H8O3/c10-8-6-4-1-2-5(3-4)7(6)9(11)12-8/h1-2,4-7H,3H2/t4-,5+,6-,7+

Formula

C₉H₈O₃

PubChem ID

2723766

Molweight

164.16

LogP

0.7

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

anhydrides

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

Dipentyl Carbonate

Compound Details

Synonymous names

Dipentyl carbonate

2050-94-4

Diamyl carbonate

Carbonic acid, dipentyl ester

carbonic acid dipentyl ester

MFCD00068969

Carbonicacid,dipentylester

dipentylcarbonate

C11H22O3

Di-N-amyl carbonate

Dipentyl carbonate #

SCHEMBL37366

Carbonic acid, di-N-amyl ester

DTXSID20278527

NSC7948

HSNQKJVQUFYBBY-UHFFFAOYSA-N

CAA05094

NSC 7948

NSC-7948

AKOS028108607

DS-19373

SY309481

CS-0163204

C73885

Microorganism:

Yes

IUPAC name

dipentyl carbonate

SMILES

CCCCCOC(=O)OCCCCC

Inchi

InChI=1S/C11H22O3/c1-3-5-7-9-13-11(12)14-10-8-6-4-2/h3-10H2,1-2H3

Formula

C₁₁H₂₂O₃

PubChem ID

222266

Molweight

202.29

LogP

4.1

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

carbonates anhydrides

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

Decan-2-yl Ethyl Carbonate

Compound Details

Synonymous names

Decan-2-yl ethyl carbonate

94720-95-3

SCHEMBL5608104

DTXSID20535526

FCVPQVAPQCTDDB-UHFFFAOYSA-N

Microorganism:

Yes

IUPAC name

decan-2-yl ethyl carbonate

SMILES

CCCCCCCCC(C)OC(=O)OCC

Inchi

InChI=1S/C13H26O3/c1-4-6-7-8-9-10-11-12(3)16-13(14)15-5-2/h12H,4-11H2,1-3H3

Formula

C₁₃H₂₆O₃

PubChem ID

13297819

Molweight

230.34

LogP

5.3

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

carbonates anhydrides

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

4-methylpentan-2-yl Propyl Carbonate

Compound Details

Synonymous names

MCTAIRCCXKYCDU-UHFFFAOYSA-N

4-Methylpentan-2-yl propyl carbonate

Microorganism:

Yes

IUPAC name

4-methylpentan-2-yl propyl carbonate

SMILES

CCCOC(=O)OC(C)CC(C)C

Inchi

InChI=1S/C10H20O3/c1-5-6-12-10(11)13-9(4)7-8(2)3/h8-9H,5-7H2,1-4H3

Formula

C₁₀H₂₀O₃

PubChem ID

91691406

Molweight

188.26

LogP

3.5

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

carbonates anhydrides

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

[(E)-hex-3-enyl] 2-methylpropyl Carbonate

Compound Details

Synonymous names

CHVMJBNPMKVDBQ-AATRIKPKSA-N

(E)-Hex-3-enyl isobutyl carbonate

Microorganism:

Yes

IUPAC name

[(E)-hex-3-enyl] 2-methylpropyl carbonate

SMILES

CCC=CCCOC(=O)OCC(C)C

Inchi

InChI=1S/C11H20O3/c1-4-5-6-7-8-13-11(12)14-9-10(2)3/h5-6,10H,4,7-9H2,1-3H3/b6-5+

Formula

C₁₁H₂₀O₃

PubChem ID

91697795

Molweight

200.27

LogP

3.6

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

carbonates anhydrides

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

Acetyl Acetate

Compound Details

Synonymous names

ACETIC ANHYDRIDE

Acetyl acetate

108-24-7

Acetanhydride

Ethanoic anhydride

Acetyl anhydride

Acetic acid, anhydride

Acetyl oxide

acetic acid anhydride

Acetic oxide

Acetyl ether

Anhydride acetique

Anidride acetica

Octowy bezwodnik

Azijnzuuranhydride

Essigsaeureanhydrid

Ethanoic anhydrate

Anhydrid kyseliny octove

Ac2O

ethanoyl ethanoate

(CH3CO)2O

Caswell No. 003A

HSDB 233

CCRIS 688

Acetic acid, 1,1'-anhydride

EINECS 203-564-8

UNII-2E48G1QI9Q

EPA Pesticide Chemical Code 044007

BRN 0385737

2E48G1QI9Q

DTXSID0024395

CHEBI:36610

Acetic anhydride-1,1'-13C2,d6

(MeCO)2O

DTXCID704395

285977-77-7

EC 203-564-8

4-02-00-00386 (Beilstein Handbook Reference)

ACETIC ANHYDRIDE-13C4, D6

ACETIC ANHYDRIDE (1,1'-13C2)

285977-78-8

ACETIC ANHYDRIDE (II)

ACETIC ANHYDRIDE [II]

MFCD00008705

Octowy bezwodnik [Polish]

Azijnzuuranhydride [Dutch]

Anidride acetica [Italian]

Anhydride acetique [French]

Essigsaeureanhydrid [German]

Anhydrid kyseliny octove [Czech]

UN1715

acetanhydrid

acetic anhydrid

actic anhydride

diacetyl oxide

acetic-anhydride

acetic, anhydride

AcOAc

Acetyltrimethyl-Silane

acetic acetic anhydride

Acetic anhydride [UN1715] [Corrosive]

acetic acid acetyl ester

SCHEMBL523

Acetic anhydride ACS grade

acetic acid-acetic anhydride

(Ac)2O

Acetic anhydride, >=99%

Acetic anhydride, 99.5%

Pesticide Code: 044007

MLS002454384

ACETIC ANHYDRIDE [MI]

Acetic anhydride, ACS, 97%

ACETIC ANHYDRIDE [HSDB]

CHEMBL1305819

HMS3039J03

BCP20665

Acetic anhydride, JIS special grade

Tox21_200278

STL264203

AKOS015915487

MCULE-9184217748

UN 1715

NCGC00091802-01

NCGC00091802-02

NCGC00257832-01

Acetic anhydride, reagent grade, >=98%

BP-24367

BP-31054

CAS-108-24-7

SMR001372001

Acetic anhydride [UN1715] [Corrosive]

Acetic anhydride, ACS reagent, >=98.0%

Acetic anhydride, ReagentPlus(R), >=99%

NS00004253

Acetic anhydride, p.a., ACS reagent, 97.0%

Acetic anhydride, SAJ first grade, >=93.0%

A801828

Acetic anhydride, Lonza quality, >=99.5% (GC)

Q407775

Acetic anhydride, for GC derivatization, >=99.0%

InChI=1/C4H6O3/c1-3(5)7-4(2)6/h1-2H

Acetic anhydride, p.a., ACS reagent, reag. ISO, reag. Ph. Eur., 99.0%

Acetic anhydride, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99% (GC)

Capping B1 (40 % acetic anhydride in acetonitrile, for AKTA oligopilottrade mark) NC-0806, GL45 thread emp Biotech GmbH

Microorganism:

Yes

IUPAC name

acetyl acetate

SMILES

CC(=O)OC(=O)C

Inchi

InChI=1S/C4H6O3/c1-3(5)7-4(2)6/h1-2H3

Formula

C₄H₆O₃

PubChem ID

7918

Molweight

102.09

LogP

-0.1

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

esters anhydrides

CHEBI-ID

36610

Supernatural-ID

SN0408579

mVOC Specific Details

Boiling Point

Degree	Reference
139.5 °C peer reviewed

Volatilization

The half-life for the hydrolysis of acetic anhydride is 4.4 minutes(SRC), based on a rate constant of 0.002625 1/sec at 25 °C(1). Hydrolysis is expected to be the predominate fate of acetic anhydride in moist soil and water (SRC). The potential for volatilization of acetic anhydride from dry soil surfaces may exist(SRC) based upon a vapor pressure of 5.1 mm Hg(2).

Soil Adsorption

Species emitting the compound

Kingdom	Species	Biological Function	Origin/Habitat	Reference
Prokaryota	Lactobacillus Plantarum		NA	Yang et al. 2022
	Saccharomyces Cerevisiae			Qin et al. 2024

Method

Kingdom	Species	Growth Medium	Applied Method	Verification
Prokaryota	Lactobacillus Plantarum	ginkgo biloba kernel juice	triple quadrupole GC-MS	no
	Saccharomyces Cerevisiae	fermentation of mulberry wine	HS-SPME-GC-MS	no

4,5,6,7-tetraphenyl-2-benzofuran-1,3-dione

Compound Details

Synonymous names

Tetraphenylphthalic anhydride

4741-53-1

4,5,6,7-tetraphenylisobenzofuran-1,3-dione

4,5,6,7-Tetraphenyl-2-benzofuran-1,3-dione

G9C5LSE3VV

NSC-46729

1,3-Isobenzofurandione, 4,5,6,7-tetraphenyl-

NSC46729

EINECS 225-253-6

3,4,5,6-Tetraphenylphthalic anhydride

UNII-G9C5LSE3VV

SCHEMBL2778432

Phthalic anhydride, tetraphenyl-

DTXSID90197130

NSC 46729

AKOS024319403

DB-051447

NS00031686

4,5,6,7-Tetraphenyl-1,3-isobenzofurandione

G73108

4,5,6,7-Tetraphenyl-2-benzofuran-1,3-dione #

[m-Terphenyl]-4',5'-dicarboxylic anhydride, 2',6'-diphenyl-

[1,1':2',1''-Terphenyl]-3',4'-dicarboxylic anhydride, 5',6'-diphenyl-

[1,1':4',1''-Terphenyl]-2',3'-dicarboxylic anhydride, 5',6'-diphenyl-

Microorganism:

Yes

IUPAC name

4,5,6,7-tetraphenyl-2-benzofuran-1,3-dione

SMILES

C1=CC=C(C=C1)C2=C(C(=C3C(=C2C4=CC=CC=C4)C(=O)OC3=O)C5=CC=CC=C5)C6=CC=CC=C6

Inchi

InChI=1S/C32H20O3/c33-31-29-27(23-17-9-3-10-18-23)25(21-13-5-1-6-14-21)26(22-15-7-2-8-16-22)28(30(29)32(34)35-31)24-19-11-4-12-20-24/h1-20H

Formula

C₃₂H₂₀O₃

PubChem ID

78478

Molweight

452.5

LogP

7.8

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

benzenoids aromatic compounds anhydrides

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

Oxolane-2,5-dione

Compound Details

Synonymous names

SUCCINIC ANHYDRIDE

108-30-5

dihydrofuran-2,5-dione

oxolane-2,5-dione

Succinic acid anhydride

Succinyl oxide

Dihydro-2,5-furandione

2,5-Diketotetrahydrofuran

Succinyl anhydride

Butanedioic anhydride

Rikacid SA

2,5-Furandione, dihydro-

Tetrahydro-2,5-dioxofuran

2,5-Dioxotetrahydrofuran

Tetrahydro-2,5-furandione

Bernsteinsaure-anhydrid

NCI-C55696

Dihydro-furan-2,5-dione

NSC 8518

CCRIS 2386

HSDB 792

Dihydro-2,5-diketotetrahydrofuran

EINECS 203-570-0

UNII-6RF4O17Z8J

MFCD00005525

BRN 0108441

6RF4O17Z8J

Bernsteinsaeureanhydrid

DTXSID7021287

CHEBI:36595

AI3-52664

SuccinicAnhydride-13C4

NSC-8518

2,5(3H,4H)-Furandione

Succinic anhydride treated BSA

DTXCID701287

EC 203-570-0

5-17-11-00006 (Beilstein Handbook Reference)

68412-02-2

Succinyloxide

SUCCINIC ANHYDRIDE (IARC)

SUCCINIC ANHYDRIDE [IARC]

Bernsteinsaure-anhydrid [German]

tetrahydrofuran-2,5-dione

2, dihydro-

EINECS 270-161-1

Oxolan-2,5-dione

WLN: T5VOVTJ

butanedioic acid anhydride

Dihydro-2, 5-furandione

Succinic anhydride, 97%

BERNSTEINSAUREANHYDRID

tetrahydro-furan-2,5-dione

Tetrahydro-2, 5-dioxofuran

SCHEMBL16123

MLS002454448

SUCCINIC ANHYDRIDE [MI]

CHEMBL1370164

NSC8518

SUCCINIC ANHYDRIDE [HSDB]

HMS3039B10

STR01303

Succinic anhydride, >=99% (GC)

Tox21_201179

STL194303

AKOS000121191

Succinic anhydride, >=97.0% (NT)

NCGC00091291-01

NCGC00091291-02

NCGC00258731-01

BP-13070

CAS-108-30-5

HY-79369

SMR001372026

DB-042683

DB-050501

Butanedioic acid,anhydride succinic anhydride

CS-0011581

NS00003241

S0107

EN300-18021

C19524

D78120

Succinic anhydride, puriss., >=99.0% (NT)

Succinic anhydride, SAJ first grade, >=99.0%

A801840

Q417847

J-002088

BUTANEDIOIC ACID,ANHYDRIDE SUCCINIC ANHYDRIDE

Z57127506

F1908-0090

InChI=1/C4H4O3/c5-3-1-2-4(6)7-3/h1-2H

Tetrahydro-2,5-furandione(National Library of Medicine, SIS; ChemIDplus Record for Succinic anhydride (108-30-5) Available from, as of July 21, 2005: http://che

Microorganism:

Yes

IUPAC name

oxolane-2,5-dione

SMILES

C1CC(=O)OC1=O

Inchi

InChI=1S/C4H4O3/c5-3-1-2-4(6)7-3/h1-2H2

Formula

C₄H₄O₃

PubChem ID

7922

Molweight

100.07

LogP

-0.5

Atoms

Bonds

H-bond Acceptor

H-bond Donor

Chemical Classification

anhydrides

CHEBI-ID

36595

Supernatural-ID

SN0326321

mVOC Specific Details

Boiling Point

Degree	Reference
261 °C peer reviewed

Volatilization

Hydrolysis is expected to be the predominate fate of succinic anhydride in moist soil and water(1). Succinic anhydride is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.5X10-3 mm Hg(2).

Soil Adsorption

Adsorption of succinic anhydride in soil is unlikely due its rapid hydrolysis(1).

Vapor Pressure

Pressure	Reference
0.50075

Species emitting the compound

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

Method

Species	Growth Medium	Applied Method	Verification
Aspergillus Flavus	inoculated potato samples	GC-MS	no
Aspergillus Niger	inoculated potato samples	GC-MS	no
Pectobacterium Carotovorum	inoculated potato samples	GC-MS	no

Results for: chemical Classification: anhydrides

Tert-butyl (2-methylpropan-2-yl)oxycarbonyl Carbonate

Compound Details

mVOC Specific Details

Hexanoyl Hexanoate

Compound Details

mVOC Specific Details

3,3-dimethyloxane-2,6-dione

Compound Details

mVOC Specific Details

(1R,2S,6R,7S)-4-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione

Compound Details

mVOC Specific Details

Dipentyl Carbonate

Compound Details

mVOC Specific Details

Decan-2-yl Ethyl Carbonate

Compound Details

mVOC Specific Details

4-methylpentan-2-yl Propyl Carbonate

Compound Details

mVOC Specific Details

[(E)-hex-3-enyl] 2-methylpropyl Carbonate

Compound Details

mVOC Specific Details

Acetyl Acetate

Compound Details

mVOC Specific Details

4,5,6,7-tetraphenyl-2-benzofuran-1,3-dione

Compound Details

mVOC Specific Details

Oxolane-2,5-dione

Compound Details

mVOC Specific Details

Results for:
chemical Classification: anhydrides