Methylthioacetate

Methyl thiolacetate

Methanethiol acetate

methyl ethanethioate

S-METHYLTHIOACETATE

OATSQCXMYKYFQO-UHFFFAOYSA-N

S-Methyl ethanethioate

S-Methyl thioacetate

AC1L2KFM

S-Methyl thioacetate, AldrichCPR

S-Methyl ethanethioate #

Thioacetic acid S-methyl ester

Ethanethioic acid, methyl ester

AC1Q68RR

ACMC-1BTZ5

PF2D4MWX79

KSC493A2H

Ethanethioic acid, S-methyl ester

UNII-PF2D4MWX79

M2286

CTK3J3023

CH3C(O)SCH3

FCH918358

OR031401

OR224946

OR224947

DTXSID3073264

ZINC2004049

CHEBI:51280

CJ-07327

1-(methylsulfanyl)ethan-1-one

AB1006061

AN-49402

CJ-30959

ZINC02004049

MFCD00014989

Ethanethioic acid,S-methyl ester (9CI)

RT-001199

Q-100182

I09-0174

AKOS006229807

FT-0659567

Acetic acid, thio-, S-methyl ester

S-Methyl thioacetate, natural, >=96%, FG

1534-08-3

EINECS 216-252-1

MolPort-006-113-372

InChI=1/C3H6OS/c1-3(4)5-2/h1-2H

Methylaminomethylidyneradical

Dimethylamine hydrobromide

Dimethylamine anhydrous

dimethylammonia

Dimethylammonium bromide

dimethylarnine

Dimethylamin

dimethylamine

Dimethylamine aqueous solution

Dimethylamine solution

dimetylamine

N-Methylmethanamine

Dimethylamine Reagent Grade

ROSDSFDQCJNGOL-UHFFFAOYSA-N

Dimethylamine, anhydrous

di-methylamine

dimethyl amine

dimethyl-amine

dimetyl amine

N-methyl-Methanamine

HNMe2

Me2NH

Dimethylamine aq

Dimethylamine (anhydrous)

Dimethylamine, in aqueous solution

N,N dimethylamine

N,N-dimethylamin

N,N-Dimethylamine

Dimethylamine, 2M in tetrahydrofuran

AC1L19RK

AC1Q40HW

AC1Q40HX

AC1Q40HY

Dimethylamine anhydrous (dot)

ACMC-1BQ2Z

N,N dimethyl amine

N,N-dimethyl amine

Dimethylamine solution 40% in water

GTPL5177

KSC175G1R

CO0036

Methanamine, N-methyl-

NSC8650

UN1032

UN1160

ARQ8157E0Q

CCRIS 981

CTK0H5318

D0643

D3292

D3936

D3948

D4198

Dimethylamine solution 2.0M in Methanol

Dimethylamine, anhydrous, >=99%

Dimethylamine(40% inverted exclamation mark<<50%)

HMDB00087

HSDB 933

CHEMBL120433

LS-696

Methanamine, N-methyl-, hydrobromide

N, N-dimethyl amine

NE10568

RL01108

(CH3)2NH

C00543

Dimethylamine, >=99.8%

LTBB000394

RCRA waste number U092

UNII-ARQ8157E0Q

WLN: 1M1

DTXSID5024057

NSC 8650

NSC-8650

NSC187661

OR000103

OR210424

OR224937

STL263869

UN 1032

CHEBI:17170

DSSTox_CID_4057

AN-43529

Dimethylamine, 40% w/w aqueous solution

DSSTox_GSID_24057

SC-22709

BDBM50416497

Dimethylamine solution (45% or less)

DSSTox_RID_77272

MFCD00008288

Dimethylamine solution 2.0 M in THF

NCIOpen2_007708

NSC-187661

RTR-003773

TR-003773

AKOS008968166

Dimethylamine solution, 2.0 M in methanol

Dimethylamine, purum, >=99.0%

RCRA waste no. U092

FT-0625114

I14-17993

Ai3-15638-X

Dimethylamine solution, 2.0 M in THF

Tox21_302439

124-40-3

Dimethylamine solution, CP, 50% in H2O

Dimethylamine, 40% w/w aqueous solution, in Ampoule

F2190-0301

N-methylmethanamine (ACD/Name 4.0)

Dimethylamine solution [UN1160] [Flammable liquid]

6912-12-5

MCULE-2809467532

NCGC00255288-01

CAS-124-40-3

EINECS 204-697-4

EINECS 230-019-1

93803-04-4

Dimethylamine solution, 40 wt. % in H2O

UN 1160 (Salt/Mix)

Dimethylamine solution [UN1160] [Flammable liquid]

506-59-2 (hydrochloride)

Dimethylamine solution (over 45% but not over 55%)

Dimethylamine solution (over 55% but not over 65%)

Dimethylamine, anhydrous [UN1032] [Flammable gas]

MolPort-001-783-813

13687-EP2269977A2

13687-EP2269990A1

13687-EP2269993A1

13687-EP2269999A1

13687-EP2270001A1

13687-EP2270006A1

13687-EP2270014A1

13687-EP2272822A1

13687-EP2272827A1

13687-EP2272832A1

13687-EP2272834A1

13687-EP2272972A1

13687-EP2272973A1

13687-EP2274983A1

13687-EP2275398A1

13687-EP2275404A1

13687-EP2275412A1

13687-EP2275414A1

13687-EP2277872A1

13687-EP2277875A2

13687-EP2280006A1

13687-EP2280008A2

13687-EP2280010A2

13687-EP2281563A1

13687-EP2281813A1

13687-EP2281818A1

13687-EP2281822A1

13687-EP2284157A1

13687-EP2284160A1

13687-EP2284169A1

13687-EP2286811A1

13687-EP2287152A2

13687-EP2287155A1

13687-EP2287161A1

13687-EP2287162A1

13687-EP2287163A1

13687-EP2287165A2

13687-EP2287166A2

13687-EP2289871A1

13687-EP2289891A2

13687-EP2292228A1

13687-EP2292597A1

13687-EP2292615A1

13687-EP2292620A2

13687-EP2292628A2

13687-EP2295415A1

13687-EP2295424A1

13687-EP2295429A1

13687-EP2295433A2

13687-EP2295437A1

13687-EP2298734A2

13687-EP2298742A1

13687-EP2298761A1

13687-EP2298764A1

13687-EP2298765A1

13687-EP2298770A1

13687-EP2298775A1

13687-EP2301928A1

13687-EP2301929A1

13687-EP2301933A1

13687-EP2301935A1

13687-EP2305250A1

13687-EP2305629A1

13687-EP2305651A1

13687-EP2305652A2

13687-EP2305667A2

13687-EP2305673A1

13687-EP2305674A1

13687-EP2305678A1

13687-EP2305679A1

13687-EP2305682A1

13687-EP2305687A1

13687-EP2308479A2

13687-EP2308510A1

13687-EP2308562A2

13687-EP2308812A2

13687-EP2308828A2

13687-EP2308849A1

13687-EP2308854A1

13687-EP2308867A2

13687-EP2308870A2

13687-EP2308873A1

13687-EP2308875A1

13687-EP2308879A1

13687-EP2308880A1

13687-EP2311796A1

13687-EP2311797A1

13687-EP2311798A1

13687-EP2311799A1

13687-EP2311802A1

13687-EP2311803A1

13687-EP2311807A1

13687-EP2311815A1

13687-EP2311818A1

13687-EP2311827A1

13687-EP2311829A1

13687-EP2311831A1

13687-EP2311834A1

13687-EP2314590A1

13687-EP2316459A1

13687-EP2316836A1

13687-EP2371811A2

13687-EP2372017A1

21503-EP2270006A1

21503-EP2292628A2

21503-EP2295402A2

21503-EP2314295A1

57342-EP2284166A1

57342-EP2298762A2

57342-EP2298769A1

57342-EP2308878A2

77294-EP2305687A1

77294-EP2308849A1

Molybdoceric acid (H8 Ce Mo12 O42), eicosahydrate

Dimethylamine, anhydrous [UN1032] [Flammable gas]

148075-EP2280005A1

148075-EP2289884A1

21249-13-8 (sulfate)

30781-73-8 (nitrate)

Dimethylamine solution, 40 wt. % in water 250g

Dimethylamine solution, purum, 33% in absolute ethanol (~5.6 M)

InChI=1/C2H7N/c1-3-2/h3H,1-2H

23307-05-3 (sulfate[1:1])

A pKa of 10.73(1) indicates dimethylamine will exist almost entirely in the cation form at pH values of 5 to 9 and therefore volatilization from water surfaces and moist soil surfaces is not expected to be an important fate process(2). Dimethylamine is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1,520 mm Hg(3).
Literature: (1) Perrin DD; Dissociation constants of organic bases in aqueous solution. IUPAC Chem Data Ser, Buttersworth, London (1965) (2) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation Washington, DC: Taylor and Francis (1985)

The adsorption isotherm for dimethylamine in 5 soils was linear and resulted in a mean Koc of 434.9(1). A Koc value of 508 was reported for dimethylamine in lake sediment(2). According to a classification scheme(3), this Koc data suggests that dimethylamine is expected to have moderate mobility in soil.
Literature: (1) Rao PSC, Davidson JM; Retention and Transformation of Selected Pesticides and Phosphorus in Soil-Water Systems, A Critical Review. Washington, DC: USEPA-600/S3-82-060 (1982) (2) von Oepen B et al; Chemosphere 22: 285-304 (1991) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

Thiacyclopropane

Aethylensulfid

ethylenesulfide

Epithioethane

Dimethylene sulfide

Ethylene episulfide

Ethylene episulphide

Sulfurane

Ethylene sulphide

Thiirane

VOVUARRWDCVURC-UHFFFAOYSA-N

Thiiran

ETHYLENE SULFIDE

AC1L1TZV

AC1Q7FYU

ACMC-1AKDG

Aethylensulfid [German]

C2H4S

2,3-Dihydrothiirene

6858AF

Thiirene,3-dihydro-

WLN: T3STJ

Ethylene sulfide, 98%

CCRIS 782

CTK1D6264

E0133

NSC89690

C19419

HSDB 5489

HE073939

HE329965

CHEMBL3184935

DTXSID3049411

ACM420122

CHEBI:30977

DSSTox_GSID_49411

NSC 89690

NSC-89690

ANW-43979

SC-19359

LS-68549

FCH1115047

DSSTox_RID_83486

MFCD00005159

DSSTox_CID_29371

TR-031645

RTR-031645

A2W5165740

AI3-52351

Thiirene, 2,3-dihydro-

UNII-A2W5165740

Tox21_202917

420-12-2

NCGC00260463-01

EINECS 206-993-9

CAS-420-12-2

MolPort-001-782-825

55446-EP2308865A1

55446-EP2292597A1

54047-EP2371811A2

54047-EP2308865A1

54047-EP2308562A2

54047-EP2308510A1

54047-EP2292593A2

54047-EP2281818A1

54047-EP2270010A1

Ethylene sulfide, purum, >=97.5% (GC)

InChI=1/C2H4S/c1-2-3-1/h1-2H

The Henry's Law constant for ethylene sulfide is estimated as 3.5X10-4 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that ethylene sulfide is expect is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 8 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as approximately 5 days(SRC). Ethylene sulfide 's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Ethylene sulfide is expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 250 mm Hg(3).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Zwolinski BJ, Wilhoit RC; Handbook of vapor pressures and heats of vaporizaton of hydrocarbons and related compounds. API44-TRC101. College Station, TX: Thermodynamcs Research Center (1971)

Slightly soluble in ethanol and ether; soluble in acetone and chloroform
Literature: Lide, D.R. CRC Handbook of Chemistry and Physics 86TH Edition 2005-2006. CRC Press, Taylor & Francis, Boca Raton, FL 2005, p. 3-484
Literature: #In water, 2.8X10+4 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver.3.12. Nov 30, 2004. Available from, as of Jul 23, 2008: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm

Using a structure estimation method based on molecular connectivity indices(1), the Koc of ethylene sulfide can be estimated to be 26(SRC). According to a classification scheme(2), this estimated Koc value suggests that ethylene sulfide is expected to have very high mobility in soil.
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-67 (1992) (2) Swann RL et al; Res Rev 85: 17-28 (1983)