Results for:
chemical Classification: sulfoxides

Methylsulfonylsulfanylmethane

Mass-Spectra

Compound Details

Synonymous names
methylsulfonylsulfanylmethane
methylmethanethiosulfonate
methylsulfonylsulfanyl-methane
Methyl methanethiosulfonate
s-methylmethanethiosulfonate
Methyl methanethiolsulfonate
Methyl methanesulfonothioate
methyl methanethiolsulfate
(METHANESULFONYLSULFANYL)METHANE
S-Methyl methanethiosulphonate
S-Methyl methanesulfonothioate
dimethyl thiosulfonate
s-methyl methanethionsulfonate
s-methyl methanethiolsulfonate
S-Methyl thiomethanesulfonate
METHYL METHANETHIO-SULFONATE
s-methyl methylthiosulfonate
S-Methyl methanethiosulfonate
XYONNSVDNIRXKZ-UHFFFAOYSA-N
methyl(methylsulfonyl)thio
S-Methyl methanethiosulfonate, analytical standard
Methyl Methanethiosulfonate-13C
Methanethiosulfonic Acid S-Methyl Ester
Methanesulfonothioic acid, S-methyl ester
Methanethiosulfonic acid, S-methyl ester
AC1L2BA2
S-Methyl methanethiosulfonate, 97%
PubChem14140
CTK3J2626
A5499
M1382
ACMC-209h9g
NE10494
NSC21545
SCHEMBL136797
CCRIS 7217
OR000547
OR207198
OR254241
DTXSID8062739
CHEMBL1236925
ZINC4268917
CHEBI:74357
NSC 21545
NSC-21545
LS-90353
SC-24153
AN-16789
ANW-26642
MFCD00007565
ZINC04268917
0906Z2356U
METHANESULFONIC ACID, THIO-, S-METHYL ESTER
TR-012818
ST51038052
AM20080910
RTR-012818
CS-W004461
AKOS006221195
I09-1550
J-017549
BRN 1446059
FT-0082457
UNII-0906Z2356U
MCULE-2094653694
2949-92-0
EINECS 220-970-0
31761-75-8
117991-82-9
MolPort-000-157-294
S-Methyl methanethiosulfonate, purum, >=98.0% (GC)
4-04-00-00031 (Beilstein Handbook Reference)
InChI=1/C2H6O2S2/c1-5-6(2,3)4/h1-2H
IUPAC namemethylsulfonylsulfanylmethane
SMILESCSS(=O)(=O)C
InchiInChI=1S/C2H6O2S2/c1-5-6(2,3)4/h1-2H3
FormulaC2H6O2S2
PubChem ID18064
Molweight126.19
LogP-0.06
Atoms12
Bonds11
H-bond Acceptor2
H-bond Donor0
Chemical ClassificationSulfates Sulfoxides thiosulfinates sulfur compounds

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaBurkholderia Sp. AD24bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
BacteriaDinoroseobacter Shibaen/aSchulz and Dickschat, 2007
BacteriaDinoroseobacter Shibae Strain DFL-27n/aDickschat et al., 2005_4
BacteriaLoktanella Sp.n/aSchulz and Dickschat, 2007
BacteriaLoktanella Sp. Bio-204n/aDickschat et al., 2005_4
BacteriaPseudomonas Chlororaphis R47narhizosphere of field-grown potato plantsHunziker et al., 2015
BacteriaPseudomonas Fluorescens R76narhizosphere of field-grown potato plantsHunziker et al., 2015
BacteriaPseudomonas Jessenii S34naphyllosphere of field-grown potato plantsHunziker et al., 2015
BacteriaPseudomonas Syringae S22naphyllosphere of field-grown potato plantsHunziker et al., 2015
BacteriaStigmatella Aurantiacan/aSchulz and Dickschat, 2007
BacteriaStigmatella Aurantiaca DW4/3-1n/aDickschat et al., 2005_5
Fungi Fusarium Sp.Dickschat et al. 2011
Fungi Penicillium Sp.Citron et al. 2013
BacteriaBurkholderia Ambifaria LMG 17828n/aBurkholderia ambifaria LMG 17828 from root, LMG 19182 from rhizosphere and LMG 19467 from clinical.Groenhagen et al., 2013
BacteriaBurkholderia Ambifaria LMG 19182n/aBurkholderia ambifaria LMG 17828 from root, LMG 19182 from rhizosphere and LMG 19467 from clinical.Groenhagen et al., 2013
BacteriaBurkholderia Ambifaria LMG 19467n/aBurkholderia ambifaria LMG 17828 from root, LMG 19182 from rhizosphere and LMG 19467 from clinical.Groenhagen et al., 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaBurkholderia Sp. AD24TSBAGC-Q-TOFno
BacteriaDinoroseobacter Shibaen/an/a
BacteriaDinoroseobacter Shibae Strain DFL-27n/an/a
BacteriaLoktanella Sp.n/an/a
BacteriaLoktanella Sp. Bio-204n/an/a
BacteriaPseudomonas Chlororaphis R47LB mediumGC/MSYes
BacteriaPseudomonas Fluorescens R76LB mediumGC/MSYes
BacteriaPseudomonas Jessenii S34LB mediumGC/MSYes
BacteriaPseudomonas Syringae S22LB mediumGC/MSYes
BacteriaStigmatella Aurantiacan/an/a
BacteriaStigmatella Aurantiaca DW4/3-1n/an/a
Fungi Fusarium Sp.no
Fungi Penicillium Sp.no
BacteriaBurkholderia Ambifaria LMG 17828Luria-Bertani medium, Malt Extractn/a
BacteriaBurkholderia Ambifaria LMG 19182Luria-Bertani medium, Malt Extractn/a
BacteriaBurkholderia Ambifaria LMG 19467Luria-Bertani medium, Malt Extractn/a


Methylsulfinylsulfanylmethane

Mass-Spectra

Compound Details

Synonymous names
methylsulfinylsulfanylmethane
methylsulfinylsulfanyl-methane
Methyl methanethiosulfinate
(methanesulfinylsulfanyl)methane
S-Methyl methanesulfinothioate
Dimethyl thiosulfinate
S-methylmethane thiosulfinate
S-Methyl thiomethanesulfinate
S-Methyl methanethiosulfinate
Methyl methane thiosulphinate
RRGUMJYEQDVBFP-UHFFFAOYSA-N
AC1L3TSC
Dimethyldisulfide, S-oxide
Methanesulfinothioic acid, S-methyl ester
SCHEMBL862565
NSC23129
CHEMBL403038
2,3-Dithiabutane2-oxide
OR217331
NSC-23129
LS-90061
AKOS006278759
BRN 1738960
13882-12-7
MolPort-038-948-769
Methanesulfinic acid, thio-, S-methyl ester (6CI,7CI,8CI)
4-04-00-00004 (Beilstein Handbook Reference)
IUPAC namemethylsulfinylsulfanylmethane
SMILESCSS(=O)C
InchiInChI=1S/C2H6OS2/c1-4-5(2)3/h1-2H3
FormulaC2H6OS2
PubChem ID95200
Molweight110.19
LogP0.45
Atoms11
Bonds10
H-bond Acceptor1
H-bond Donor0
Chemical ClassificationSulfides Sulfoxides thiosulfinates sulfur compounds

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaDinoroseobacter Shibaen/aSchulz and Dickschat, 2007
BacteriaLoktanella Sp.n/aSchulz and Dickschat, 2007
BacteriaStigmatella Aurantiacan/aSchulz and Dickschat, 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaDinoroseobacter Shibaen/an/a
BacteriaLoktanella Sp.n/an/a
BacteriaStigmatella Aurantiacan/an/a


[2-(benzenesulfinylmethyl)-3-phenylcyclopropyl]benzene

Compound Details

Synonymous names
MVULGCSHGFLUBH-UHFFFAOYSA-N
AC1LBQJR
(2,3-diphenylcyclopropyl)methyl phenyl sulfoxide
[2-(benzenesulfinylmethyl)-3-phenylcyclopropyl]benzene
CHEBI:84273
(2,3-Diphenylcyclopropyl)methyl phenyl sulfoxide, trans-
(2-Phenyl-3-[(phenylsulfinyl)methyl]cyclopropyl)benzene #
1,1'-{3-[(phenylsulfinyl)methyl]cyclopropane-1,2-diyl}dibenzene
IUPAC name[2-(benzenesulfinylmethyl)-3-phenylcyclopropyl]benzene
SMILESC1=CC=C(C=C1)C2C(C2C3=CC=CC=C3)CS(=O)C4=CC=CC=C4
InchiInChI=1S/C22H20OS/c23-24(19-14-8-3-9-15-19)16-20-21(17-10-4-1-5-11-17)22(20)18-12-6-2-7-13-18/h1-15,20-22H,16H2
FormulaC22H20OS
PubChem ID562543
Molweight332.46
LogP4.48
Atoms44
Bonds47
H-bond Acceptor1
H-bond Donor0
Chemical ClassificationSulfoxides benzenoids

mVOC Specific Details

Solubility
1.06e-02 g/l
Literature: ALOGPS

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaPseudomonas Putida BP25nablack pepper rootSheoran et al., 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaPseudomonas Putida BP25Luria Bertani AgarSolvent extraction with hexane, GC/MSNo


Methylsulfanyl(methylsulfinyl)methane

Mass-Spectra

Compound Details

Synonymous names
methanesulfinyl(methylsulfanyl)methane
Methanesulfinyl-methylsulfanyl-methane
Methyl methylmercaptomethyl sulfoxide
methyl methylsulphinylmethyl sulphide
methylsulfanyl(methylsulfinyl)methane
methyl methylsulfinylmethyl sulfide
Methyl methylthiomethyl sulphoxide
Methylsulfinyl(methylthio)methane
Methyl methylthiomethyl sulfoxide
methyl (methylthiomethyl)sulphoxide
OTKFCIVOVKCFHR-UHFFFAOYSA-N
methyl methylsulfinyl-methyl sulfide
methylsulfinyl (methylthio)methane
Formaldehyde Dimethyl Dithioacetal S-Oxide
FAMSO
(Methylsulfanyl)(methylsulfinyl)methane
(Methylthio)dimethyl sulfoxide
Formaldehyde dimethyl mercaptal S-oxide
Formaldehyde methyl mercaptal S-oxide
Methyl((methylsulfinyl)methyl)sulfane
methyl (methylthiomethyl) sulphoxide
Methyl (methylsulfinyl)methyl sulfide
Methyl (methylthiomethyl) sulfoxide
Methyl (methylthio)methyl sulfoxide
(Methylsulfinyl)(methylthio)methane
Sulfide, methyl (methylsulfinyl)methyl
AC1L40OD
(Methylsulfanyl)(methylsulfinyl)methane;(methylsulfinyl)(methylthio)-methan
M0805
CTK4H0906
Methane,(methylsulfinyl)(methylthio)-
SCHEMBL364365
RL03236
ACMC-209i1t
A23492
OR259344
OR012361
NSC181492
X-3724
ANW-27663
BP-12695
Methane, (methylsulfinyl)(methylthio)-
SC-87090
KB-54793
MFCD00002091
DB-026948
NSC 181492
NSC-181492
TR-014039
AKOS000278611
J-522615
FT-0628753
MCULE-3167702486
EINECS 251-577-2
95833-60-6
33577-16-1
MolPort-006-126-736
IUPAC namemethylsulfanyl(methylsulfinyl)methane
SMILESCSCS(=O)C
InchiInChI=1S/C3H8OS2/c1-5-3-6(2)4/h3H2,1-2H3
FormulaC3H8OS2
PubChem ID99129
Molweight124.22
LogP-0.56
Atoms14
Bonds13
H-bond Acceptor1
H-bond Donor0
Chemical Classificationsulfoxides thioethers sulfur compounds

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiTuber Magnatumn/aItalian geographical areas ( Umbria, Piedmont, Marche, Emilia Romagna, Border region area between Emilia Romagna and Marche, Tuscany, Molise)Gioacchini et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


Methylsulfinylmethane

Mass-Spectra

Compound Details

Synonymous names
methanesulfinylmethane
Methylsulfinylmethane
methylsulfmylmethane
dimethyisulphoxide
Dimethylsulphoxide
sulfinylbismethane
dimethvlsulfoxide
dimethyisulfoxide
Dimethylsulfoxid
Dimethylsulfoxide
Dimethylsulfoxyde
Dimethylsulphinyl
Dimetilsolfossido
sulfinyldimethane
(methanesulfinyl)methanedimethyl sulfoxide
methylsulfoxide
DMSO, sterile filtered|Methyl sulfoxide|Dimethyl sulfoxide
dimethyl suiphoxide
Dimethyl sulfoxixde
Dimethyl sulphoxide
dimethyl-sulphoxide
Dimethyli sulfoxidum
Dipirartril-tropico
dirnethyl sulfoxide
Infiltrina
Sulfinylbis-methane
Demasorb
Demsodrox
Dermasorb
Diemthyl sulfoxide
dimethyl sulfoxide
Dimethyl sulpoxide
dimethyl-sulfoxide
Dimetil sulfoxido
dimetyl sulfoxide
Dimexide
Dimexidum
Dromisol
Durasorb
IAZDPXIOMUYVGZ-UHFFFAOYSA-N
Methyl sulphoxide
Sclerosol
Somipront
Syntexan
(methanesulfinyl)methane
(methylsulfinyl)methane;Dimethyl sulfoxide
Deltan
Demavet
Demeso
Diluent
Dimethyl Sulfoxide Irrigation USP
Dolicur
Doligur
Domoso
Hyadur
Kemsol
Methyl sulfoxide
Topsym
(methylsulfinyl)methane
Decap
DMSO
Rimso
Dimethyl sulfoxide BP
Dimethyl sulfoxide, analytical standard
Dimethyl sulfoxide, anhydrous
Dimethyl sulfur oxide
Dimethyl- -Chloropropionamide
Sulfinylbis(methane)
dimethyl sulf oxide
qCbPPAD]h@
Sulfoxide, dimethyl
AC1Q4GSG
C2H6OS
DIMETHYL SULFOXIDE, ACS
Dimethyl sulfoxide, for molecular biology
Dimetilsolfossido [DCIT]
CHEMBL504
Dimethyl sulfoxide, HPLC Grade
Dimethyl sulfoxide, PCR Reagent
Dimethylsulfoxyde [INN-French]
DMSO; Methyl sulfoxide
Methane, sulfinylbis-
Methyl Sulfoxide: DMSO
Sulfinyl bis(methane)
2-Thiapropane2-oxide
AC1L19RZ
Dimethyl sulfoxide, for HPLC
Domoso (Veterinary)
Rimso-5
DIMETHYL SULFOXIDE- D6
Gamasol 90
NSC763
Topsym (rescinded)
(DMSO)
Dimethyl sulfoxide, >=99%
HSDB 80
Kemsol Liquid 70%
KSC353A9L
Rimso 50
Rimso-50
ACMC-1BH88
Dimethyl sulfoxide, ACS reagent
Dimethyl sulfoxide, meets EP testing specifications, meets USP testing specifications
Dimethyli sulfoxidum [INN-Latin]
Dimetil sulfoxido [INN-Spanish]
DMS 70
DMS 90
DMS-70
DMS-90
CCRIS 943
CTK2F3095
D0601
D0798
Dimethyl sulfoxide [USAN:INN]
Dimethyl sulfoxide, European Pharmacopoeia (EP) Reference Standard
Dimethyl sulfoxide, meets EP, USP testing specifications
HMDB02151
Rimso 100
S(O)Me2
Sulfinylbis-methane (9CI)
YOW8V9698H
BIDD:PXR0182
DB01093
Dimethyl sulfoxide (USP/INN)
NSC 763
NSC-763
RL04586
RP18373
WLN: OS1&1
(CH3)2SO
C11143
D01043
Dimethyl sulfoxide, United States Pharmacopeia (USP) Reference Standard
DMSO, 80% aqueous solution
LTBB002677
M 176
Methyl sulfoxide (8CI)
METHYL, (METHYLSULFINYL)-
UNII-YOW8V9698H
DTXSID2021735
LS-1568
NSC760436
OR034986
OR228317
OR228318
OR247990
OR343745
SQ 9453
SQ-9453
STL264194
300067X
CHEBI:28262
Dimethyl sulfoxide, >=99.5%
DSSTox_CID_1735
ZINC5224188
AB1004054
AB1004058
AN-20755
AN-23766
ANW-42740
Dimethyl sulfoxide [USAN:USP:INN:BAN]
Dimethyl sulfoxide, LR, >=99%
DSSTox_GSID_21735
SC-16101
TL8004767
A 10846
BDBM50026472
Caswell No. 381
DSSTox_RID_76298
Methyl sulfoxide, >=99%, FG
MFCD00002089
ZINC05224188
AI3-26477
CCG-213615
Dimethyl sulfoxide, ACS spectrophotometric grade, >=99.9%
Methane, 1,1'-sulfinylbis-
NSC-760436
RTR-022725
TR-022725
AKOS000121107
Dimethyl sulfoxide, anhydrous, >=99.9%
EPA Pesticide Chemical Code 000177
Methane, sulfinylbis- (9CI)
FT-0625099
MRF-0000764
Rimso-50 (TN)
67-68-5
Dimethyl sulfoxide, >=99.0%, suitable for absorption spectrum analysis
I14-14298
Dimethyl sulfoxide, ACS reagent, >=99.9%
Dimethyl sulfoxide, AR, >=99.5%
Dimethyl sulfoxide, sterile-filtered, BioPerformance Certified, meets EP, USP testing specifications, suitable for hybridoma
Tox21_300957
(Methyl sulfoxide)-d6; DMSO-d6; Hexadeuterodimethyl sulfoxide
Dimethyl sulfoxide, UV HPLC spectroscopic, 99.9%
CAS-67-68-5
Dimethyl sulfoxide, 99% 500g
Dimethyl sulfoxide, for HPLC, >=99.5%
Dimethyl sulfoxide, for HPLC, >=99.7%
Dimethyl sulfoxide, HPLC grade, 99.9%
Dimethyl sulfoxide, JIS special grade, >=99.0%
8070-53-9
Dimethyl sulfoxide, >=99.6%, ReagentPlus(R)
Dimethyl sulfoxide, ReagentPlus(R), >=99.5%
Dimethyl sulfoxide, SAJ first grade, >=99.0%
Dimethyl sulfoxide, Vetec(TM) reagent grade, 99%
MCULE-2005841258
NCGC00163958-01
NCGC00163958-02
NCGC00163958-03
NCGC00254859-01
AB01563146_01
EINECS 200-664-3
Dimethyl sulfoxide, AldraSORB(TM), 99.8%
Pharmakon1600-01506122
METHYL-13C SULFOXIDE, 99 ATOM %13C
164071-41-4
705301-21-9
Dimethyl sulfoxide solution, 50 wt. % in H2O
1926-EP1441224A2
1926-EP2269977A2
1926-EP2269978A2
1926-EP2269979A1
1926-EP2269985A2
1926-EP2269989A1
1926-EP2269990A1
1926-EP2269991A2
1926-EP2269992A1
1926-EP2269993A1
1926-EP2269994A1
1926-EP2269996A1
1926-EP2270003A1
1926-EP2270004A1
1926-EP2270006A1
1926-EP2270008A1
1926-EP2270010A1
1926-EP2270011A1
1926-EP2270012A1
1926-EP2270013A1
1926-EP2270014A1
1926-EP2270015A1
1926-EP2270018A1
1926-EP2272509A1
1926-EP2272510A1
1926-EP2272517A1
1926-EP2272813A2
1926-EP2272817A1
1926-EP2272822A1
1926-EP2272825A2
1926-EP2272827A1
1926-EP2272834A1
1926-EP2272835A1
1926-EP2272839A1
1926-EP2272840A1
1926-EP2272841A1
1926-EP2272842A1
1926-EP2272844A1
1926-EP2272848A1
1926-EP2272972A1
1926-EP2272973A1
1926-EP2274983A1
1926-EP2275102A1
1926-EP2275403A1
1926-EP2275409A1
1926-EP2275412A1
1926-EP2275413A1
1926-EP2275414A1
1926-EP2275416A1
1926-EP2275420A1
1926-EP2275421A1
1926-EP2275422A1
1926-EP2275425A1
1926-EP2277848A1
1926-EP2277858A1
1926-EP2277866A1
1926-EP2277872A1
1926-EP2277875A2
1926-EP2277876A1
1926-EP2277878A1
1926-EP2277881A1
1926-EP2277898A2
1926-EP2277945A1
1926-EP2279741A2
1926-EP2279750A1
1926-EP2280001A1
1926-EP2280006A1
1926-EP2280008A2
1926-EP2280009A1
1926-EP2280011A1
1926-EP2280012A2
1926-EP2280013A1
1926-EP2280014A2
1926-EP2281559A1
1926-EP2281563A1
1926-EP2281810A1
1926-EP2281813A1
1926-EP2281815A1
1926-EP2281817A1
1926-EP2281819A1
1926-EP2281823A2
1926-EP2281899A2
1926-EP2284150A2
1926-EP2284151A2
1926-EP2284152A2
1926-EP2284153A2
1926-EP2284154A1
1926-EP2284155A2
1926-EP2284156A2
1926-EP2284157A1
1926-EP2284159A1
1926-EP2284160A1
1926-EP2284164A2
1926-EP2284166A1
1926-EP2284167A2
1926-EP2284168A2
1926-EP2284172A1
1926-EP2284174A1
1926-EP2284178A2
1926-EP2284179A2
1926-EP2286811A1
1926-EP2286915A2
1926-EP2287140A2
1926-EP2287148A2
1926-EP2287150A2
1926-EP2287153A1
1926-EP2287156A1
1926-EP2287163A1
1926-EP2287164A1
1926-EP2287165A2
1926-EP2287166A2
1926-EP2287168A2
1926-EP2289871A1
1926-EP2289876A1
1926-EP2289882A1
1926-EP2289883A1
1926-EP2289885A1
1926-EP2289886A1
1926-EP2289890A1
1926-EP2289891A2
1926-EP2289892A1
1926-EP2289893A1
1926-EP2289894A2
1926-EP2292088A1
1926-EP2292227A2
1926-EP2292228A1
1926-EP2292233A2
1926-EP2292234A1
1926-EP2292576A2
1926-EP2292589A1
1926-EP2292590A2
1926-EP2292592A1
1926-EP2292593A2
1926-EP2292595A1
1926-EP2292597A1
1926-EP2292606A1
1926-EP2292609A1
1926-EP2292611A1
1926-EP2292613A1
1926-EP2292614A1
1926-EP2292615A1
1926-EP2292617A1
1926-EP2292619A1
1926-EP2292620A2
1926-EP2292630A1
1926-EP2295053A1
1926-EP2295055A2
1926-EP2295401A2
1926-EP2295402A2
1926-EP2295406A1
1926-EP2295407A1
1926-EP2295408A1
1926-EP2295410A1
1926-EP2295411A1
1926-EP2295412A1
1926-EP2295413A1
1926-EP2295414A1
1926-EP2295415A1
1926-EP2295416A2
1926-EP2295417A1
1926-EP2295418A1
1926-EP2295419A2
1926-EP2295422A2
1926-EP2295423A1
1926-EP2295424A1
1926-EP2295425A1
1926-EP2295426A1
1926-EP2295427A1
1926-EP2295429A1
1926-EP2295432A1
1926-EP2295433A2
1926-EP2295434A2
1926-EP2295439A1
1926-EP2295503A1
1926-EP2295550A2
1926-EP2298305A1
1926-EP2298312A1
1926-EP2298731A1
1926-EP2298732A1
1926-EP2298734A2
1926-EP2298735A1
1926-EP2298736A1
1926-EP2298742A1
1926-EP2298743A1
1926-EP2298744A2
1926-EP2298745A1
1926-EP2298746A1
1926-EP2298747A1
1926-EP2298748A2
1926-EP2298750A1
1926-EP2298761A1
1926-EP2298764A1
1926-EP2298765A1
1926-EP2298767A1
1926-EP2298768A1
1926-EP2298769A1
1926-EP2298770A1
1926-EP2298773A1
1926-EP2298774A1
1926-EP2298776A1
1926-EP2298778A1
1926-EP2298779A1
1926-EP2298780A1
1926-EP2298783A1
1926-EP2301534A1
1926-EP2301536A1
1926-EP2301538A1
1926-EP2301627A1
1926-EP2301909A1
1926-EP2301912A2
1926-EP2301913A1
1926-EP2301914A1
1926-EP2301916A2
1926-EP2301922A1
1926-EP2301923A1
1926-EP2301925A1
1926-EP2301926A1
1926-EP2301928A1
1926-EP2301929A1
1926-EP2301930A1
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Dimethyl sulfoxide, Vetec(TM) reagent grade, anhydrous, >=99.7%
Dimethyl sulfoxide, >=99.5% (GC), plant cell culture tested
Dimethyl sulfoxide, BioUltra, for molecular biology, >=99.5% (GC)
Dimethyl sulfoxide, p.a., ACS reagent, 99.9%
Dimethyl sulfoxide, for inorganic trace analysis, >=99.99995% (metals basis)
Dimethyl sulfoxide, puriss. p.a., dried, <=0.02% water
InChI=1/C2H6OS/c1-4(2)3/h1-2H
Dimethyl sulfoxide, Hybri-Max(TM), sterile-filtered, BioReagent, suitable for hybridoma, >=99.7%
Dimethyl sulfoxide, puriss. p.a., ACS reagent, >=99.9% (GC)
Dimethyl sulfoxide, puriss., absolute, over molecular sieve (H2O <=0.005%), >=99.5% (GC)
IUPAC namemethylsulfinylmethane
SMILESCS(=O)C
InchiInChI=1S/C2H6OS/c1-4(2)3/h1-2H3
FormulaC2H6OS
PubChem ID679
Molweight78.13
LogP-1.41
Atoms10
Bonds9
H-bond Acceptor1
H-bond Donor0
Chemical ClassificationSulfoxides sulfur compounds sulfinyl compounds

mVOC Specific Details

Volatilization
The Henry's Law constant for dimethyl sulfoxide is 1.03X10-8 atm-cu m/mole at 25 deg C(SRC) based upon a measured air/water partition coefficient equation of 136,600-1570T where T is in deg C and the partition coefficient is in mol/kg-atm(1). This Henry's Law constant indicates that dimethyl sulfoxide is expected to be essentially nonvolatile from moist soil and water surfaces(2). The observation that the concentration of dimethyl sulfoxide in marine air is about 1/100 that of dimethyl sulfide suggests that little or no dimethyl sulfoxide is volatilizing from the sea surface(3). Dimethyl sulfoxide's Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to be an important(SRC). Dimethyl sulfoxide is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure 0.60 mm Hg at 25 deg C(4).
Literature: (1) Watts SF, Brimblecombe P; Environ Technol Lett 8: 483-86 (1987) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Harvey GR, Lang RG; Geophys Res Let 13: 49-51 (1986) (4) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (2002)
Literature: #The volatilization rate of a pool of dimethyl sulfoxide was measured at 0 and -17.5 deg C(1). The flux was found to be proportional to the cube root of the wind speed. At a wind speed of 1 m/s, the volatilization rate was approximately 1.2 and 9 ug/min at -17.5 and 0 deg C, respectively. The calculated volatilization rate at zero wind velocity is 0.8 and 0.07 ug/min at 0 and -20 deg C, respectively(1). For volatilization of droplets, as opposed to a pool, surface affects (droplet spreading), would be important(SRC).
Literature: (1) Podoll RT, Parish HJ; Experimental Measurements of the Properties of Chemical Surety Materials Under Conditions of Extreme Cold. CREDC-CR-88051 AD B122 961 Aberdeen Proving Ground, MD: US Army CREDC (1988)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of dimethyl sulfoxide can be estimated to be 2(SRC). According to a classification scheme(2), this estimated Koc value suggests that dimethyl sulfoxide is expected to have very high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of June 16, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.60 mm Hg at 25 deg CDaubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (2002)
MS-Links
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaTsukamurella Sp. AD106nanaTyc et al., 2015
FungiTuber Aestivumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al., 2003
FungiTuber Melanosporumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al., 2003
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaTsukamurella Sp. AD106Tryptic soy broth agarGC/MS-Q-TOFNo
FungiTuber Aestivumn/an/a
FungiTuber Melanosporumn/an/a