ethanecarboxylate

Carboxyethane

Ethanecarboxylic acid

metacetonate

methylacetate

PropionicAcid

Propionsaeure

pseudoacetate

Kyselina propionova

propanoate

propionate

acide propanoique

Acide propionique

Luprisol

Luprosil

methylacetic acid

Monoprop

Propcorn

Propkorn

Pseudoacetic acid

XBDQKXXYIPTUBI-UHFFFAOYSA-N

ethylformic acid

Metacetonic acid

Propionoic acid

Prozoin

NATURAL PROPIONIC ACID

Propanoic acid

Propanyl acid

Propioic acid

propionic acid

Sentry grain preserver

Antischim B

Propionic acid grain preserver

propoic acid

Methyl acetic acid

Propionic Acid Reagent Grade

Toxi-Check

AC1L1AKT

AC1Q2SKR

C2H5COOH

n-propionic acid

Propionic acid, analytical standard

Tenox P grain preservative

2-methylacetic acid

Methylacetic Acid, Propanoic Acid

JHU490RVYR

1-propanoic acid

Acid C3

C3 acid

Acide propionique [French]

C3H6O2

Kyselina propionova [Czech]

UNII-JHU490RVYR

E280

GTPL1062

KSC377K4B

Propionic acid (natural)

S067

CHEMBL14021

UN1848

C1-5 Carboxylic acids

C3:0

CH3-CH2-COOH

CTK2H7540

HMDB00237

P0500

Propionic acid, >=99%

DB03766

Propionic acid (NF)

Propionic acid [NF]

Propionic acid, 99%

Propionic Acid, Ethanecarboxylic Acid, Methylacetic Acid, Propanoic Acid

RL05053

bmse000179

C00163

CCRIS 6096

D02310

HSDB 1192

LTBB001652

DNC000832

DTXSID8025961

FEMA Number 2924

LS-1771

OR033967

OR226045

OR246996

OR253314

OR328316

Propanoic acid (9CI)

Propionic acid [USAN:NF]

STL168039

UN 1848

ACMC-20977b

Carboxylic acids, C1-5

CHEBI:30768

DSSTox_CID_5961

ETHYL, 1-CARBOXY-

ETHYL, 2-CARBOXY-

Propionic acid, United States Pharmacopeia (USP) Reference Standard

ZINC6050663

ANW-13605

BP-20411

DSSTox_GSID_25961

KB-59985

PROPOXY, 1-OXO-

SC-22887

BDBM50082199

Caswell No. 707

LMFA01010003

MFCD00002756

Propionic acid, >=99.5%

AI3-04167

Propionic acid, 99.5%

RTR-025212

TR-025212

AKOS000118853

EPA Pesticide Chemical Code 077702

Epitope ID:139981

I04-0849

Propionic acid (6CI,8CI)

Propionic acid, 99%, FCC

BRN 0506071

Fatty acids, C3-24

FEMA No. 2924

FT-0658557

79-09-4

Propionic acid, 99% 1kg

Tox21_304030

(C3-C24) Fatty acids

F2191-0098

CAS-79-09-4

Propionic acid, ACS reagent, >=99.5%

Propionic acid, for synthesis, 99.5%

Propionic acid, natural, 99%, FG

MCULE-2199051150

NCGC00357239-01

Propionic acid, BioReagent, suitable for insect cell culture, ~99%

EINECS 201-176-3

EINECS 273-079-4

EINECS 273-598-6

Propionic acid, feed grade, 98.7%

68937-68-8

68990-37-4

Propionic acid [UN1848] [Corrosive]

Propionic acid, SAJ first grade, >=98.0%

613-EP2269610A2

613-EP2269986A1

613-EP2269988A2

613-EP2270008A1

613-EP2270011A1

613-EP2270113A1

613-EP2272935A1

613-EP2275401A1

613-EP2275407A1

613-EP2275413A1

613-EP2277848A1

613-EP2277858A1

613-EP2277867A2

613-EP2277878A1

613-EP2277880A1

613-EP2280003A2

613-EP2280013A1

613-EP2280014A2

613-EP2281563A1

613-EP2281819A1

613-EP2284146A2

613-EP2284147A2

613-EP2284159A1

613-EP2284160A1

613-EP2284169A1

613-EP2284174A1

613-EP2287152A2

613-EP2287153A1

613-EP2287155A1

613-EP2287156A1

613-EP2287161A1

613-EP2287162A1

613-EP2287168A2

613-EP2289510A1

613-EP2289883A1

613-EP2289890A1

613-EP2289965A1

613-EP2292597A1

613-EP2292599A1

613-EP2292606A1

613-EP2292609A1

613-EP2292610A1

613-EP2292617A1

613-EP2292619A1

613-EP2295055A2

613-EP2295409A1

613-EP2295424A1

613-EP2295435A1

613-EP2295438A1

613-EP2298731A1

613-EP2298735A1

613-EP2298747A1

613-EP2298757A2

613-EP2298763A1

613-EP2298772A1

613-EP2298779A1

613-EP2298828A1

613-EP2301918A1

613-EP2301922A1

613-EP2301924A1

613-EP2301931A1

613-EP2301937A1

613-EP2301940A1

613-EP2305257A1

613-EP2305633A1

613-EP2305641A1

613-EP2305646A1

613-EP2305649A1

613-EP2305651A1

613-EP2305659A1

613-EP2305666A1

613-EP2305683A1

613-EP2305684A1

613-EP2305808A1

613-EP2308838A1

613-EP2308839A1

613-EP2308848A1

613-EP2308851A1

613-EP2308854A1

613-EP2308857A1

613-EP2308858A1

613-EP2308869A1

613-EP2309584A1

613-EP2311453A1

613-EP2311796A1

613-EP2311797A1

613-EP2311798A1

613-EP2311799A1

613-EP2311801A1

613-EP2311802A1

613-EP2311803A1

613-EP2311807A1

613-EP2311809A1

613-EP2311811A1

613-EP2311816A1

613-EP2311817A1

613-EP2311818A1

613-EP2311824A1

613-EP2311830A1

613-EP2311839A1

613-EP2311842A2

613-EP2311850A1

613-EP2314586A1

613-EP2314588A1

613-EP2314589A1

613-EP2314590A1

613-EP2314593A1

613-EP2316457A1

613-EP2316458A1

613-EP2316459A1

613-EP2316825A1

613-EP2316826A1

613-EP2316827A1

613-EP2316828A1

613-EP2316837A1

613-EP2316937A1

613-EP2371803A1

613-EP2371814A1

613-EP2377843A1

613-EP2380568A1

784139-72-6

MolPort-000-871-576

Top distillation cut by-product acids, monobasic (C1-C5)

1032826-44-0

Propionic acid [UN1848] [Corrosive]

Propionic acid, >=99.5%, FCC, FG

11906-EP2269978A2

11906-EP2269985A2

11906-EP2269991A2

11906-EP2284150A2

11906-EP2284151A2

11906-EP2284152A2

11906-EP2284153A2

11906-EP2284155A2

11906-EP2284156A2

11906-EP2284164A2

11906-EP2287140A2

11906-EP2287148A2

11906-EP2287150A2

11906-EP2289871A1

11906-EP2292590A2

11906-EP2295419A2

11906-EP2298732A1

11906-EP2301534A1

11906-EP2301912A2

11906-EP2301913A1

11906-EP2301914A1

11906-EP2301916A2

11906-EP2305637A2

11906-EP2308832A1

11906-EP2308863A1

11906-EP2311451A1

11906-EP2311796A1

11906-EP2311797A1

11906-EP2311798A1

11906-EP2311799A1

11906-EP2316450A1

32532-EP2295430A2

32532-EP2295431A2

32532-EP2301544A1

32532-EP2301933A1

32532-EP2305825A1

32532-EP2311824A1

32532-EP2311827A1

557-28-8 (zinc salt)

4-02-00-00695 (Beilstein Handbook Reference)

Propionic acid, puriss. p.a., >=99.5% (GC)

InChI=1/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5

A pKa of 4.87(1) indicates propionic acid will exist almost entirely in the anion form at pH values of 5 to 9 and therefore volatilization from water surfaces is not expected to be an important fate process(2). Propionic acid is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure of 3.35 mm Hg(3).
Literature: (1) Serjeant EP, Dempsey B; Ionization Constants of Organic Acids in Aqueous Solution. Inter Union Pure Appl Chem (IUPAC). IUPAC Chem Data Ser No. 23. NY, NY: Pergamon Press, Inc. (1979) (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; Data Compilation, Tables of Properties of Pure Cmpds, Design Inst for Phys Prop Data. NY, NY: Am Inst for Phys Prop Data (1985)

The Koc of propionic acid is estimated as 36(SRC), using a log Kow of 0.33(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that propionic acid is expected to have very high mobility in soil. The pKa of propionic acid is 4.87(4), indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5).
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 6 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983) (4) Serjeant EP, Dempsey B; Ionization Constants of Organic Acids in Aqueous Solution. Inter Union Pure Appl Chem (IUPAC). IUPAC Chem Data Ser No. 23. NY, NY: Pergamon Press, Inc. (1979) (5) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

METHYLSULFANYLMETHANE

Methanethiomethane

Dimethylsulphide

Methylthiomethane

dimethylsulfane

Dimethylsulfid

dimethylsulfide

Methylsulphide

Methylthiomethyl radical

Thiobismethane

(Methylthiomethylidyne)radical

methylsulfide

Dimethyl monosulfide

Thiopropane

dimethyl sulphide

Dimethyl thioether

Methyl monosulfide

QMMFVYPAHWMCMS-UHFFFAOYSA-N

reduced dimethyl sulfoxide

dimethyl sulfide

Methyl sulphide

Methyl thioether

Thiobis-methane

(Methylsulfanyl)methane

Methyl sulfide

REDUCED-DMSO

(methylthio)methane

Dimethyl sulfide, analytical standard

Dimethyl sulfoxide(Reduced)

Sulfure de methyle

(Methylsulfanyl)methane #

2-Thiapropane

2-Thiopropane

AC1L1ANN

Exact-S

Thiobis(methane)

ACMC-1BBLH

C2H6S

Dimethylsulfid [Czech]

Nat. Dimethyl Sulfide

Dimethyl sulfide (natural)

Methane, thiobis-

QS3J7O7L3U

KSC377G0P

Sulfide, methyl-

6873AF

CHEMBL15580

Dimethyl sulfide, >=99%

UN1164

UNII-QS3J7O7L3U

CTK2H7307

Dimethyl sulfide, 98%

HMDB02303

HSDB 356

M0431

[SMe2]

RP18263

Sulfure de methyle [French]

C00580

LTBB002388

(CH3)2S

DTXSID9026398

LS-2960

methyl sulphide, dimethyl sulphide, exact-S, thiobismethane

OR000121

OR337379

STL481894

UN 1164

A838342

CHEBI:17437

AN-23841

ANW-36574

KB-76628

SC-26847

Dimethyl sulfide, >=99%, FCC

MFCD00008562

AI3-25274

RTR-024212

TR-024212

AKOS009031411

I09-0087

Q-100810

BRN 1696847

Dimethyl sulfide, anhydrous, >=99.0%

FEMA No. 2746

FT-0603084

Methane, 1,1'-thiobis-

75-18-3

Dimethyl sulfide, 99% 250ml

MCULE-4525381422

Dimethyl sulfide, redistilled, >=99%, FCC, FG

EINECS 200-846-2

31533-72-9

Dimethyl sulfide [UN1164] [Flammable liquid]

Dimethyl sulfide, >=95.0% (GC)

Dimethyl sulfide, natural, >=99%, FCC, FG

MolPort-003-928-951

Dimethyl sulfide [UN1164] [Flammable liquid]

13741-EP2269977A2

13741-EP2277865A1

13741-EP2280006A1

13741-EP2284171A1

13741-EP2287153A1

13741-EP2298767A1

13741-EP2305656A1

13741-EP2308851A1

13741-EP2308873A1

13741-EP2311820A1

13741-EP2314576A1

13741-EP2314587A1

13741-EP2316836A1

13838-EP2292595A1

13838-EP2295409A1

13838-EP2295426A1

13838-EP2295427A1

13838-EP2295437A1

13838-EP2298775A1

13838-EP2311820A1

13838-EP2316836A1

18767-EP2270003A1

18767-EP2272832A1

18767-EP2277848A1

18767-EP2292576A2

18767-EP2292597A1

18767-EP2301933A1

18767-EP2305672A1

18767-EP2308510A1

18767-EP2308838A1

18767-EP2308877A1

18767-EP2311827A1

18767-EP2314576A1

18767-EP2314587A1

47704-EP2280006A1

47704-EP2311811A1

80926-EP2295426A1

80926-EP2295427A1

80926-EP2305687A1

Dimethyl sulfide, puriss., >=99.0% (GC)

InChI=1/C2H6S/c1-3-2/h1-2H

4-01-00-01275 (Beilstein Handbook Reference)

The Henry's Law constant for dimethyl sulfide has been measured as 1.61X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that dimethyl sulfide is expected to volatilize rapidly 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 3 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 3 days(SRC). Dimethyl sulfides's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of dimethyl sulfide from dry soil surfaces may exist(SRC) based upon a vapor pressure of 502 mm Hg(3).
Literature: (1) Gaffney, JS et al; Env Sci Tech 21: 519-23 (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) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Vol 4. Design Inst Phys Prop Data, Amer Inst Chem Eng, NY, NY: Hemisphere Pub Corp (1989)

The Koc of dimethyl sulfide is estimated as 6.3(SRC), using a water solubility of 22,000 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that dimethyl sulfide is expected to have very high mobility in soil.
Literature: (1) Suzuki T; J Comp-Aided Molec Des 5: 149-66 (1991) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm as of Oct 1, 2009. (3) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #Air-dried, unsterilized moist, and sterilized moist soils exposed to air initially containing 500 ppm dimethyl sulfide adsorbed an avg of 32, 308, and 10 ug dimethyl sulfide/g soil, respectively, in 15 days(1). Time required for complete sorption of dimethyl sulfide by moist soil from air initially containing 100 ppm dimethyl sulfide: soil 1 (Weller) - 1st exposure 150 min, 2nd exposure 100 min, 3rd exposure 95 min; soil 2 (Harps) - 1st exposure 45 min, 2nd exposure 24 min, 3rd exposure 19 min(1). These data suggest that moist soils have a greater tendency to adsorb dimethyl sulfide than dry soils, and that microbial activity in moist soils may be responsible for greater adsorption(1). When natural gas containing 0.5 pounds of dimethyl sulfide per million cubic feet of gas was passed through a bed of pulverized, dry, montmorillonite clay, dimethyl sulfide exhibited a fast breakthrough (2 hours) and a fast build-up rate in effluent gas (85% of influent concn 4 hours after breakthrough), suggesting that dimethyl sulfide does not adsorb to dry soils(2).
Literature: (1) Bremner JM, Banwart WL; Soil Biol Biochem 8: 79-83 (1976) (2) Williams RP; Oper Sect Proc - Am Gas Assoc pp. T29-T37 (1976)

UUIQMZJEGPQKFD-UHFFFAOYSA-N

Methyl butanoate

Methyl butyrate

methyl 3-methylpropionate

Methyl butyrate, analytical standard

Methyl n-butanoate

Butyric acid methyl

Nat.Methyl Butyrate

Butanoicacid, methyl ester

Butanoic acid methyl ester

METHYL N-BUTYRATE

Methyl-n-butyrate

Butyric acid methyl ester

AC1L1Z0X

Methyl ester of butanoic acid

n-Butyric acid methyl ester

Butyric acid, methyl ester

Butanoic acid, methyl ester

Methyl butyrate (natural)

KSC492E1L

n-C3H7COOCH3

NSC9380

CHEMBL15859

SCHEMBL13685

UN1237

B0763

CTK3J2215

S0302

ACMC-209t4w

NE61132

RP18773

Methyl butyrate, 99%

ZINC404765

HSDB 5721

WLN: 3VO1

CGX598508O

DTXSID5047083

Methyl butyrate, certified reference material, TraceCERT(R)

SBB061104

OR010874

LS-2914

NSC 9380

NSC-9380

ZB013579

UN 1237

CHEBI:88806

UNII-CGX598508O

TRA0052853

SC-74735

CJ-04054

ANW-42030

TL8004117

DSSTox_GSID_47083

AN-22009

n-Butyric acid methyl ester [standard material]

KB-54743

MFCD00009391

ZINC00404765

DSSTox_CID_27083

DSSTox_RID_82095

LMFA07010528

Methyl butyrate, >=98%, FG

RTR-021432

ST51047170

TR-021432

AI3-06009

AKOS008907317

J-522595

FT-0628708

FEMA No. 3693

FEMA No. 2693

BRN 1740743

I14-19354

Tox21_301821

Methyl butyrate, natural, >=98%, FG

623-42-7

NCGC00256040-01

MCULE-1092030267

CAS-623-42-7

EINECS 210-792-1

Methyl butyrate [UN1237] [Flammable liquid]

WE(1:0/4:0)

MolPort-003-927-474

36683-EP2311803A1

Methyl butyrate [UN1237] [Flammable liquid]

36683-EP2371814A1

36683-EP2311802A1

36683-EP2311801A1

36683-EP2305825A1

36683-EP2305642A2

4-02-00-00786 (Beilstein Handbook Reference)

5ADC8486-F8C0-4A7A-ACD5-2234D52DE6E0

InChI=1/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H

The Henry's Law constant for methyl n-butyrate is 2.05X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that methyl n-butyrate 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 4 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 5 days(SRC). Methyl n-butyrate's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of methyl n-butyrate from dry soil surfaces may exist(SRC) based upon a vapor pressure of 32.3 mm Hg(3).
Literature: (1) Buttery RG et al; J Agric Food Chem 17: 385-89 (1969) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Yaws CL; Handbook of Vapor Pressure. Vol 2 C5-C7 Compounds. Houston, TX: Gulf Pub Co (1994)

The Koc of methyl n-butyrate is estimated as 120(SRC), using a log Kow of 1.29(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that methyl n-butyrate is expected to have high mobility in soil(SRC).
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 14 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

alpha-Nonylethylene

Undecene

Hendecene

DCTOHCCUXLBQMS-UHFFFAOYSA-N

alpha-Undecylene

alpha-Undecene

AC1Q2VYM

1-Hendecene

Undecene-1

1-UNDECENE

Undecene (petroleum)

n-1-Undecene

Undec-1-ene

.alpha.-Undecene

5902AF

C11H22

ACMC-1CB71

U0025

U0052

CTK1A4960

S0341

UNII-FH2735S2NU component DCTOHCCUXLBQMS-UHFFFAOYSA-N

OR01835

NSC73983

AC1L2186

HSDB 1090

CCRIS 5720

DTXSID5061168

SBB009051

LP064094

STL453737

FR-2625

CHEBI:77444

ZINC1699445

KB-13370

CC-05049

ANW-37513

NSC-73983

NSC 73983

LMFA11000332

ZX-AT017311

MFCD00008956

1-Undecene, 97%

C-28171

LS-188198

ST51046389

TR-025719

1446756A8F

DB-056580

AKOS009156849

FT-0608327

UNII-1446756A8F

I14-19830

821-95-4

10004-001h

MCULE-8437878932

EINECS 212-483-7

EINECS 271-214-1

28761-27-5

MolPort-001-756-623

The Henry's Law constant for 1-undecene is estimated as 1.48 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 1-undecene is expected to volatilize rapidly 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 1 hr(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 5 days(SRC). However, the volatilization half-life does not take into account the effects of adsorption. This is apparent from the results of two EXAMS model runs, one in which the effect of adsorption was considered, yielding an estimated half-life of 21 days in a model pond 2 m deep, and one in which the effect of adsorption was ignored, yielding an estimated half-life of 42 hrs in a model pond 2 m deep(3). 1-Undecene's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). 1-Undecene is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.493 mm Hg(4).
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) USEPA; EXAMS II Computer Simulation (1987) (4) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng NY, NY: Hemisphere Pub Corp 5 Vol (1989)

Sol in ether, chloroform, ligroin; insol in water
Literature: Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-327

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 1-undecene can be estimated to be about 3180(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1-undecene is expected to have slight 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)

Hydrogenated polydecene

Hydrogenated decene homopolymer

Polydecene

AFFLGGQVNFXPEV-UHFFFAOYSA-N

Decylene

alpha-Decene

Decene, homopolymer

n-Decylene

AC1Q2VXA

ACMC-1BMFN

1-Decene homopolymer

1-DECENE

decene-1

Linealene 10

AC1L21LX

Gulftene 10

Neodene 10

Dialene 10

1-Decene, analytical standard

KSC204C7R

1-Decene, homopolymer

5760AF

.alpha.-Decene

n-1-Decene

Dec-1-ene

1-n-Decene

C10H20

1-Decene, homopolymer, hydrogenated

D0028

S0340

CTK1A4178

NSC62122

Poly(1-decene)

Decene, n-

HSDB 1073

CCRIS 5718

7O4U4C718P

DTXSID8027329

LP082263

SBB058674

CHEMBL3187990

DSSTox_CID_7329

ZINC1691021

UNII-7O4U4C718P

CHEBI:87315

ANW-38642

KB-12040

AN-20561

AN-17673

NSC-62122

TRA0012887

LS-59413

NSC 62122

1-C10H20

DSSTox_GSID_27329

LMFA11000311

DSSTox_RID_78410

MFCD00009577

DB-056981

1-Decene, 94%

ST51037219

RTR-027298

W-107244

AKOS015902910

FT-0607692

I14-19927

I14-53239

Tox21_200195

1-Decene, 96%, remainder isomers

F8881-0779

3B1-003551

872-05-9

1-DECENE MFC10 H20

(C10-C16) alpha-Olefin

MCULE-1391753135

Alkenes, C10-16 alpha-

NCGC00257749-01

NCGC00248557-01

CAS-872-05-9

EINECS 212-819-2

EINECS 272-492-7

25189-70-2

68037-01-4

37309-58-3

215723-62-9

221043-31-8

108778-38-7

330625-93-9

330625-94-0

157185-82-5

105054-87-3

375348-80-4

122525-37-5

MolPort-001-756-622

1-Decene, >=97.0% (GC)

1-Decene, purum, >=95.0% (GC)

InChI=1/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H

The Henry's Law constant for 1-decene is estimated as 2.68 atm-cu m/mole(SRC) from its vapor pressure, 1.67 mm Hg(1), and water solubility, 0.115 mg/l(2). This Henry's Law constant indicates that 1-decene is expected to volatilize rapidly from water surfaces(3). 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)(3) is estimated as 1.2 hrs(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 5 days(SRC). However, the volatilization half-life does not take into account the effects of adsorption. This is apparent from the results of two EXAMS model runs, one in which the effect of adsorption was considered, yielding an estimated half-life of 11 days in a model pond 2 m deep, and one in which the effect of adsorption was ignored, yielding an estimated half-life of 56 hours in a model pond 2 m deep(4). 1-Decene's Henry's Law constant(1,2) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 1-decene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 1.67 mm Hg(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng NY, NY: Hemisphere Pub Corp 5 Vol (1989) (2) Shaw DG; Hydrocarbons with water and seawater. Part II Hydrocarbons C8 to C36. International Union of Pure and Applied Chemistry. Solubility Data Series. Vol 38 pp. 561 (1989) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) USEPA; EXAMS II Computer Simulation (1987)

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 1-decene can be estimated to be about 1720(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1-decene is expected to have low 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)

Acetylfuran

IEMMBWWQXVXBEU-UHFFFAOYSA-N

2-acetylfurane

2-Furylethanone

Furyl methyl ketone

2-Acetylfuran

AC1Q1JXY

AC1L23YX

ACMC-1BPS0

PubChem6939

2-Acetyl furan

I896

KSC175C9R

Methyl 2-furyl ketone

2-Furyl methyl ketone

SCHEMBL43960

NSC4665

CTK0H5198

A0091

2-Aminomethyl-azetidine-1-carboxylic acid tert-butylester

1-Furan-2-ylmethanone

Q5ZRP80K02

NSC49133

2-Furyl methyl ketone, analytical standard

STR05504

AM91073

RP18952

ZINC157401

CCRIS 3161

Ketone, 2-furyl methyl

UNII-Q5ZRP80K02

NSC 4665

NSC-4665

PS-4586

SBB040248

HE110254

HE017372

STK400329

ZB006673

DTXSID0051601

BBL027427

CHEBI:59983

A804234

AJ-15008

NSC-49133

NSC 49133

1-Furan-2-yl-ethanone

LS-87211

KB-12200

SC-00529

AB1001236

AC-11853

ST2415091

AK-53418

Furan, 2-acetyl-

ANW-17304

AN-20640

TRA0078485

CJ-01650

1-(2-FURANYL)ETHANONE

1-(2-Furyl)ethanone

BB_SC-6820

2-Furyl methyl ketone (natural)

MFCD00003242

ZINC00157401

DB-003253

RTR-003241

AI3-23586

TR-003241

ST50213408

AKOS000119584

Epitope ID:136039

I14-0303

Q-100089

1-(2-Furyl)ethanone #

1-(furan-2-yl)ethanone

1-(2-Furanyl)-ethanone

2-Furyl methyl ketone, 99%

BRN 0107909

(2-furanyl)-1-ethanone

FEMA No. 3163

FT-0610977

I14-22249

Ethanone, 1-(furanyl)-

F0001-0316

1-(furan-2-yl)-ethanone

MCULE-6389695813

1192-62-7

EINECS 214-757-1

2-Furyl methyl ketone, >=99%, FG

80145-44-4

Ethanone, 1-(2-furanyl)-

1-(2-Furanyl)ethanone; 2-Furyl methyl ketone

1-(Furan-2-yl)ethan-1-one

MolPort-000-871-221

2-Furyl methyl ketone, natural (US), >=97%, FG

5-17-09-00381 (Beilstein Handbook Reference)

2-Furyl methyl ketone, purum, >=99.0% (GC)

InChI=1/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H

NBXLPPVOZWYADY-UHFFFAOYSA-N

AC1L2LPO

AC1Q6ZH1

8739AA

2-Ethyl-5-methylfuran

2-Methyl-5-ethylfuran

CTK0I4245

SCHEMBL144611

AK123311

HE027925

FCH831781

CHEBI:88617

ZINC1995224

2-Ethyl-5-methyl-furan

DTXSID80168839

AX8247489

AJ-32274

KB-230411

AKOS006228280

I14-48848

Furan, 2-ethyl-5-methyl-

1703-52-2

EINECS 216-937-5

BTTIKHRJTKRJFR-UHFFFAOYSA-N

AC1LD3O8

CTK2H1110

SCHEMBL198297

OR094733

2,2-dimethyl-4-pentenylamine

DTXSID20348956

ZINC32302256

AKOS006340254

2,2-dimethyl-pent-4-enyl-amine

5-amino-4,4-dimethyl-1-pentene

2,2-dimethylpent-4-en-1-amine

2,2-dimethyl-4-penten-1-amine

73604-46-3

MolPort-022-364-713

4-penten-1-amine, 2,2-dimethyl-

InChI=1/C7H15N/c1-4-5-7(2,3)6-8/h4H,1,5-6,8H2,2-3H

YCBSHDKATAPNIA-FNORWQNLSA-N

AC1NSJKU

3-Nonene

UNII-M0TB9RXK4B component YCBSHDKATAPNIA-FNORWQNLSA-N

trans-3-Nonene

non-3-ene

N0383

LP029403

ZINC1632732

FCH1117712

FCH4077806

697F6717WI

MFCD00009533

ACM20063927

ACM20063778

UNII-697F6717WI

(E)-3-Nonene

TRANS-3-NONENE 99+%

(E)-Non-3-ene

EINECS 243-495-0

(E)-3-C9H18

3-Nonene, (E)-

20063-92-7

20063-77-8

JABYJIQOLGWMQW-VQHVLOKHSA-N

AC1NSCAW

4-Undecene

trans-4-Undecene

M7DNF68P2D

UNII-M7DNF68P2D

UNII-FH2735S2NU component JABYJIQOLGWMQW-VQHVLOKHSA-N

LP031184

NSC244852

4-Undecene, trans-

LMFA11000436

(E)-4-Undecene

NSC-244852

(E)-undec-4-ene

(4E)-4-Undecene #

693-62-9

4-Undecene, (E)-

20810-21-3

MHLPKAGDPWUOOT-UHFFFAOYSA-N

housane

AC1L1SBG

AC1Q1GVV

CTK0H7543

OR235091

CHEBI:49287

BICYCLO(2.1.0)PENTANE

BICYCLO[2,1,0]PENTANE

Bicyclo[2.1.0]pentane

KB-200582

185-94-4

XDODWINGEHBYRT-OCAPTIKFSA-N

1alpha,2alpha-Cyclohexanedimethanol

cis-1,2-Cyclohexanedimethanol

cis-Cyclohexane-1,2-diyldimethanol

AC1MC439

CTK4C9388

cis-1,2-cyclohexane-dimethanol

Cis-1,2-cyclohexane dimethanol

OR40058

SCHEMBL129425

AK129072

1,2-Cyclohexanedimethanol, cis-

AJ-68466

KB-48942

ANW-21698

AX8121474

FCH3467190

MFCD00062987

ZINC16137764

TC-110443

cis-1,2-Cyclohexanedimethanol, 97%

J-009421

AKOS015915800

FT-0690197

I14-52872

(1S,2S)-1,2-CyclohexanediMethanol

15753-50-1

[(1S,2R)-2-(hydroxymethyl)cyclohexyl]methanol

MolPort-001-767-658

1,2-Cyclohexanedimethanol,(1R,2S)-rel-

1,2-Cyclohexanedimethanol, (1R,2S)-rel-

Isopentenes

MHNNAWXXUZQSNM-UHFFFAOYSA-N

gamma-Isoamylene

2-Methylbutene

1-Isoamylene

AC1L1WXD

ACMC-1ARWQ

2-methyl butene

2-methyl-butene

.gamma.-Isoamylene

2-Methylbutene-1

UN2371

UN2459

2 -methyl butene

CTK1A1560

OR14507

UNII-F238I92ISV component MHNNAWXXUZQSNM-UHFFFAOYSA-N

NSC72414

2-Methylbut-1-ene

HSDB 5695

33C9Y0I55H

2-METHYL-1-BUTENE

1-BUTENE,2-METHYL

OR012139

UN 2459

C2H5C(CH3)=CH2

UNII-33C9Y0I55H

CHEBI:77915

ZINC1698512

Butene, 2-methyl-

CJ-28526

ANW-32490

2-Methyl-1-butene, analytical standard

AN-23702

NSC-72414

NSC 72414

KB-25182

2-Methyl-1-butene, technical

MFCD00009333

TR-019788

AKOS009157996

FT-0612897

1-Butene, 2-methyl-

I14-47142

563-46-2

2-Methyl-1-butene, 98%

EINECS 247-975-0

EINECS 209-250-7

70266-76-1

77996-59-9

26760-64-5

11069-33-3

Isopentenes [UN2371] [Flammable liquid]

MolPort-001-760-702

2-Methyl-1-Butene (99% Min.)

2-Methyl-1-butene [UN2459] [Flammable liquid]

InChI=1/C5H10/c1-4-5(2)3/h2,4H2,1,3H

The Henry's Law constant for 2-methyl-1-butene calculated from its vapor pressure, 610 mm Hg(1), and water solubility, 130 mg/l(2), is 0.43 atm-cu m/mole (SRC). This Henry's Law constant indicates that 2-methyl-1-butene should volatilize rapidly from water surfaces(3). 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)(3) is estimated as 2.4 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)(3) is estimated as 3.3 days(SRC). 2-Methyl-1-butene's Henry's Law constant(1,2) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 2-methyl-1-butene from dry soil surfaces exists based upon its vapor pressure of 610 mm Hg(1).
Literature: (1) Daubert TE, Danner RP; Data Compilation Tables of Properties of Pure Compounds NY, NY: Amer Inst for Phys Prop Data (1989) (2) Suzuki T; J Computer-aided Molecular Design 5: 149-66 (1991) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

Sol in alcohol, ether, benzene
Literature: Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-105
Literature: #In water, 130 mg/l @ 20 deg C.
Literature: Suzuki T et al; J Computer-aided Molecular Design 5: 149-66 (1991)

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 2-methyl-1-butene can be estimated to be 68(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2-methyl-1-butene is expected to have 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)

2-[(octyloxy)methyl]cyclobutanone

2-(octoxy-methyl)-cyclobutan-1-one

p-Methoxyphenylbutanone

Anisylacetone

p-Methoxybenzylacetone

4-Methoxybenzylacetone

PCBSXBYCASFXTM-UHFFFAOYSA-N

Methyl oxanone

ANISYL ACETONE

Raspberry ketone methyl ether

Rasberry ketone methyl ether

AC1Q4CHA

AC1L1UCC

Methoxybenzylacetone, p-

Anisylacetone, p-

SCHEMBL1334

GVG47S4S5V

L571

KSC496A2J

UNII-GVG47S4S5V

CTK3J6024

M0756

VF10076

OR13500

BBL027730

Jsp000420

OR022040

NSC405366

CHEMBL3184371

OR154376

DTXSID5047166

AK163318

LS-2896

SBB002546

ST092728

STL146341

ZB016111

ACMC-2098b8

ZINC1235108

DSSTox_GSID_47166

AN-24670

CJ-04791

CC-16593

KB-34461

AX8017381

ANW-15042

ZX-AT014618

MFCD00008791

DSSTox_RID_82167

DSSTox_CID_27166

C-24497

BB_NC-2171

ZERO/005545

DB-003441

AI3-20279

RT-002825

ST24042959

NSC-405366

NSC 405366

I01-5625

BB_NC-02171

AKOS000120662

W-108822

ENT 20,279

1-(p-Methoxyphenyl)-3-butanone

FT-0616645

FEMA No. 2672

BRN 1869592

4-(p-Methoxyphenyl)-2-butanone

Tox21_301165

Tox21_113654

BBV-46872299

104-20-1

1-(4-Methoxyphenyl)-3-butanone

4-(4-Methoxyphenyl)-2-butanone

4-(4-Methoxyphenyl)butan-2-one

1-(p-Methoxyphenyl)-3-butanone-

NCGC00248312-02

NCGC00248312-01

NCGC00255063-01

MCULE-5951016256

EINECS 203-184-2

CAS-104-20-1

4-(4-Methoxyphenyl)-2-butanone, analytical standard

4-(4-methoxyphenyl)-butan-2-one

SR-01000944748

2-Butanone, 4-(p-methoxyphenyl)-

4-(p-Methoxyphenyl)-2-butanone (natural)

MolPort-001-758-492

4-(4-methoxy-phenyl)-butan-2-one

2-BUTANONE, 4-(4-METHOXYPHENYL)-

4-(4-Methoxyphenyl)-2-butanone, 98%

SR-01000944748-1

4-(4-Methoxyphenyl)-2-butanone, >=98%, FCC, FG

2-Butanone, 4-(p-methoxyphenyl)- (6CI,7CI,8CI)

dimethylhydroxylamine

dimethyl-hydroxylamine

VMESOKCXSYNAKD-UHFFFAOYSA-N

N,N-DIMETHYLHYDROXYLAMINE

N,N-dimethylhydroxyamine

AC1L1ECA

N,N-dimethyl-hydroxylamine

[Hydroxy(methyl)amino]methane #

CTK8J3974

M0DV42C08K

UNII-M0DV42C08K

OR034766

DTXSID5063990

Methanamine, N-hydroxy-N-methyl-

ZINC59543689

AKOS006228086

5725-96-2

34689-88-8

67012-EP2308839A1

67012-EP2298772A1

16645-06-0 (hydrochloride)