indole

1H-Indole

120-72-9

2,3-Benzopyrrole

Indol

1-Benzazole

Ketole

1-Azaindene

Benzopyrrole

2,3-Benzopyrole

Indole (natural)

Caswell No. 498B

1-Benzo(b)pyrrole

Indol [German]

FEMA No. 2593

CCRIS 4421

HSDB 599

EPA Pesticide Chemical Code 025000

1H-Benzo[b]pyrrole

Benzo[b]pyrrole

AI3-01540

NSC 1964

EINECS 204-420-7

MFCD00005607

UNII-8724FJW4M5

INDOLUM

DTXSID0020737

CHEBI:16881

8724FJW4M5

NSC-1964

CHEMBL15844

DTXCID40737

Indole 100 microg/mL in Acetonitrile

NCGC00167539-01

INDOLE (USP-RS)

INDOLE [USP-RS]

IND

CAS-120-72-9

benzazole

mono-indole

1-H-indole

Indole, 7

Indole (8CI)

Indole (white flake)

Indole, 98%

1H-Indole (9CI)

INDOLUM [HPUS]

INDOLE [FHFI]

INDOLE [HSDB]

INDOLE [FCC]

INDOLE [MI]

Indole, >=99%

SCHEMBL698

bmse000097

Indole, analytical standard

Indole, >=99%, FG

WLN: T56 BMJ

BIDD:GT0304

SCHEMBL940818

INDOLE BENZO-PYRROLE

SCHEMBL1921769

SCHEMBL9559244

AMY3411

NSC1964

185l

BCP27232

STR01201

Tox21_112536

Tox21_201677

Tox21_302937

BBL011739

BDBM50094702

s6358

STL163380

Indole, 3-Benzopyrrole, 1-benzazole

AKOS000119629

Tox21_112536_1

AT36838

CG-0501

CS-W001132

DB04532

HY-W001132

Indole, puriss., >=98.5% (GC)

MCULE-9442796928

NCGC00167539-02

NCGC00167539-03

NCGC00256348-01

NCGC00259226-01

BP-10563

DS-011308

I0021

NS00010849

EN300-18285

C00463

I-0800

I-0810

Q319541

SR-01000944736

SR-01000944736-1

Z57833933

F2190-0647

InChI=1/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9

82451-55-6

The Henry's Law constant for indole is estimated as 5.3X10-7 atm-cu m/mole(SRC) from its experimental values for vapor pressure, 0.0122 mm Hg(1), and water solubility, 3560 mg/l(2). This value indicates that indole will be essentially nonvolatile from water surfaces(3,SRC). Indole's Henry's Law constant(1,2,SRC) indicates that volatilization from moist soil surfaces should not occur(SRC).
Literature: (1) Yaws CL; Handbook of Vapor Pressure. Volume 3. C8 to C28 Compounds. HOuston,TX: Gulf Publ Co (1994) (2) Yalkowsky SH, Dannenfelser RM; Aquasol Database of Aqueous Solubility. Ver 5. College of Pharmacy, University of Arizona - Tucson, AZ. PC Ver (1992) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

A Koc of 187 was measured for indole on a synthetic soil consisting of 88-90% sand, 10% clay and 0-2% humic acid(1). The Koc of indole is estimated as approximately 350(SRC), using a measured log Kow of 2.14(2) and a regression-derived equation(3,SRC). According to a recommended classification scheme(4), these Koc values suggest that indole has moderate mobility in soil(SRC).
Literature: (1) Rebhun M et al; Water Res 26: 79-84 (1992) (2) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Amer Chem Soc, Washington, DC. p. 6 (1995) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 4-9 (1990) (4) Swann RL et al; Res Rev 85: 23 (1983)

2-METHYLPYRIDINE

2-Picoline

109-06-8

o-Picoline

alpha-Picoline

Picoline

Pyridine, 2-methyl-

METHYLPYRIDINE

a-picoline

2-METHYL-PYRIDINE

o-Methylpyridine

PICOLINE, ALPHA

.alpha.-Picoline

1333-41-1

RCRA waste number U191

NSC 3409

2-Mepy

.alpha.-Methylpyridine

2-Methylpyridine-d7

DTXSID9021899

CHEBI:50415

NSC-3409

Pyridine, methyl-

3716Q16Q6A

NCGC00160644-01

Pyridine-2,3,4,5-d4,6-(methyl-d3)-

alpha-Methylpyridine

DTXCID001899

CAS-109-06-8

CCRIS 1721

HSDB 101

EINECS 203-643-7

RCRA waste no. U191

AI3-2409

methyl pyridine

Alpha picoline

2-methylpridine

AI3-24109

UNII-3716Q16Q6A

2--picoline

2-Methyl pyridine

Picoline, .alpha.

MFCD00006332

2-Picoline, 98%

?-METHYLPYRIDINE

2-Methylpyridine, 98%

EC 203-643-7

NCIOpen2_007826

NCIOpen2_007919

WLN: T6NJ B1

BIDD:ER0295

CHEMBL15732

.ALPHA.-PICOLINE [MI]

2-Picoline, analytical standard

2-METHYLPYRIDINE [HSDB]

NSC3409

2-Picoline,(S);2-Methylpyridine

BCP26524

Tox21_111951

Tox21_201693

STL268873

AKOS000119190

AM81276

MCULE-3857746542

NCGC00160644-02

NCGC00259242-01

DB-023694

o-Picoline [UN2313] [Flammable liquid]

NS00005757

P0415

EN300-19108

A15108

2-Methylpyridine, Lonza quality, >=99.0% (GC)

J-510091

Q2216745

AMPROLIUM HYDROCHLORIDE IMPURITY A [EP IMPURITY]

F0001-0192

Z104472800

InChI=1/C6H7N/c1-6-4-2-3-5-7-6/h2-5H,1H

2-Methylpyridine pound>>o-Picoline pound>>Pyridine, 2-methyl-

38762-42-4

The Henry's Law constant for 2-methylpyridine is 9.96X10-6 atm-cu m/mole(1). This Henry's Law constant indicates that 2-methylpyridine 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 days(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 30 days(SRC). 2-Methylpyridine's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). 2-Methylpyridine is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 11.2 mm Hg at 25 deg C(3). 2-Methylpyridine is a weak base with a pKa of 5.96(4), which indicates this compound will partially exist in the protonated form in acidic conditions, and no volatilization from water or moist soil will occur for the cation(SRC). In mineral salts-soil suspensions incubated at 28 deg C, 15% was volatilized in 24 days(5). Volatilization from soil alone was only 2-3% after 60 days(6).
Literature: (1) Andon RJL et al; J Amer Chem Soc 76: 3188-96 (1954) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Chao J et al; J Phys Chem Ref Data 12: 1033-63 (1983) (4) Scriven EFV et al; Pyridine and Pyridine Derivatives. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: Dec 2, 2005. (5) Sims GK, Sommers LE; Environ Toxicol Chem 5: 503-9 (1986) (6) Sims GK, Sommers LE; J Environ Qual 14: 480-4 (1985)

The sorption behavior of 2-methylpyridine was studied in soil column tests using 5 Eurosoil reference soils having organic carbon content ranging from 0.33-1.85% and pH ranging from 5.2-8.6(1); measured Kd values ranging from 0.08 to 6.52(1) correspond to calculated Koc values of 4, 38, 70, 100 and 215(SRC); the lowest Koc value of 4 corresponds to Eurosoil 2 which had the highest pH value(8.6). The pKa of 2-methylpyridine is 5.96(2), indicating that this compound will exist partially in cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(3). In the Eurosoil column tests(1), lowest adsorption occurred when 2-methylpyridine was in non-ionized form(1). Sorption of 2-methylpyridine to soil is primarily controlled by cation exchange and surface complex formation(1,4). According to a classification scheme(5), the Koc values suggest that 2-methylpyridine is expected to have very high to moderate mobility in soil.
Literature: (1) Bi E et al; Environ Sci Technol 40: 5962-5970 (2006) (2) Scriven EFV et al; Pyridine and Pyridine Derivatives. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: Dec 2, 2005. (3) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000) (4) Bi E et al; Environ Sci Technol 41: 3172-3178 (2006) (5) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #Spectral studies of 2-methylpyridine adsorbed to hydrated and dehydrated silica indicate that hydrogen bonding occurs with silica surface silanols via the nitrogen atom on the pyridine ring and that this interaction is stronger than that between this compound and water(1). 2-Methylpyridine emerged under 2 soil column void volumes; soil columns were packed with soil cores from Rock Springs, WY to the original 1016 mm depth and shale-oil process water was used as the mobile phase(2); the pH and clay content of the soil were not specified(2); this indicates that soil is an effective adsorbent when less than this void volume of retort water is applied (as in small spills)(2); rainfall leaching after a spill will also probably enhance solute migration(2). When 2-methylpyridine was incubated at 28 deg C in a soil inoculum, 4.8% was sorbed by soil(3).
Literature: (1) Ringwald SC, Pemberton JE; Environ Sci Technol 34: 259-65 (2000) (2) Leenheer JA, Stuber HA; Environ Sci Technol 15: 1467-75 (1981) (3) Sims GK, Sommers LE Environ Toxicol Chem 5: 503-9 (1986)

2-Ethyl-5-methylpyridine

18113-81-0

Pyridine, 2-ethyl-5-methyl-

5-Methyl-2-ethyl pyridine

2-ETHYL-5-METHYL-PYRIDINE

6-Ethyl-3-picoline

5-Methyl-2-ethylpyridine

2WWW2MR72E

SCHEMBL469189

DTXSID20334051

CHEBI:179424

SB54346

BS-49493

DB-365092

E78001

EN300-7613348

ETHYL BENZOATE

93-89-0

Benzoic acid, ethyl ester

Benzoic ether

Ethyl benzenecarboxylate

Benzoic Acid Ethyl Ester

Benzoyl ethyl ether

Ethylester kyseliny benzoove

FEMA No. 2422

Ethyl benzoate (natural)

NSC 8884

EINECS 202-284-3

UNII-J115BRJ15H

J115BRJ15H

DTXSID3038696

AI3-01352

Benzoic acid-ethyl ester

NSC-8884

CHEMBL510714

BENZOIC ACID,ETHYL ESTER

DTXCID1018696

CHEBI:156074

NSC 8884-d5

EC 202-284-3

MFCD00009109

Ethylester kyseliny benzoove [Czech]

HYDROUS BENZOYL PEROXIDE IMPURITY C (EP IMPURITY)

HYDROUS BENZOYL PEROXIDE IMPURITY C [EP IMPURITY]

Ethyl benzoate, >=99%

WLN: 2OVR

ETHYL BENZOATE [MI]

SCHEMBL55674

ETHYL BENZOATE [FCC]

ETHYL BENZOATE [FHFI]

ETHYL BENZOATE [INCI]

Ethyl benzoate, puriss., 98%

FEMA 2422

NSC8884

Ethyl benzoate, analytical standard

Tox21_302021

BBL010500

BDBM50304448

STK025151

Ethyl benzoate, >=99%, FCC, FG

AKOS003596787

CS-W018155

HY-W017439

MCULE-1461486723

CAS-93-89-0

NCGC00255586-01

70750-02-6

70750-03-7

70750-04-8

VS-02532

DB-002644

B0069

Ethyl benzoate, natural, >=99%, FCC, FG

NS00008338

EN300-16131

Ethyl benzoate, Vetec(TM) reagent grade, 98%

Q421100

J-502070

Z53835169

F8880-7461

InChI=1/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H

ACETOPHENONE

98-86-2

1-Phenylethanone

Methyl phenyl ketone

Phenyl methyl ketone

Acetylbenzene

Ethanone, 1-phenyl-

Hypnone

Benzoyl methide

Acetophenon

Acetylbenzol

1-phenylethan-1-one

1-Phenyl-1-ethanone

Benzoylmethide

Acetofenon

Benzene, acetyl-

Ketone, methyl phenyl

Phenylethanone

Hypnon

USAF EK-496

methylphenylketone

phenylmethylketone

RCRA waste number U004

1-phenyl-ethanone

Acetofenon [Czech]

Dymex

NSC 7635

FEMA No. 2009

FEMA Number 2009

CCRIS 1341

HSDB 969

AI3-00575

RCRA waste no. U004

EINECS 202-708-7

UNII-RK493WHV10

RK493WHV10

DTXSID6021828

CHEBI:27632

Ketone, methyl phenyl-

NSC-7635

Acetophenone-alpha-13C

Acetophenone-1,2-13C2

CHEMBL274467

DTXCID501828

EC 202-708-7

Ethanone-2,2,2-d3, 1-(phenyl-d5)-

ACETOPHENONE (II)

ACETOPHENONE [II]

Acetofenona

CAS-98-86-2

MFCD00064447

AC0

(2,2,2,-2H3)ACETOPHENONE

aceto phenone

aceto-phenone

acetyl-benzen

Acetyl-Benzene

alpha-Acetophenone

Ethanone,1-phenyl

methyl-phenyl ketone

Methyl phenyl-Ketone

nchem.180-comp5

Benzoyl methide hypnone

1-Phenylethanone, 9CI

ACETOPHENONE [MI]

SCHEMBL737

ACETOPHENONE [FCC]

bmse000286

ACETOPHENONE [FHFI]

ACETOPHENONE [HSDB]

ACETOPHENONE [INCI]

WLN: 1VR

Acetophenone, >=98%, FG

SCHEMBL8170205

1-Phenylethanone (acetophenone)

SCHEMBL13341485

Acetophenone, analytical standard

FEMA 2009

NSC7635

Acetophenone, >=98.0% (GC)

Acetophenone, natural, 98%, FG

HY-Y0989

STR00017

Tox21_202422

Tox21_300343

Acetophenone, ReagentPlus(R), 99%

BDBM50236986

c0117

MFCD00008724

s5528

AKOS000119011

CCG-266074

DB04619

MCULE-4710225344

USEPA/OPP Pesticide Code: 129033

NCGC00248000-01

NCGC00248000-02

NCGC00254370-01

NCGC00259971-01

SY073923

DB-044220

A0061

CS-0015982

NS00010659

EN300-18050

Acetophenone, puriss. p.a., >=99.0% (GC)

C07113

D71016

A854783

Q375112

J-519533

Z57127548

Acetophenone, TraceCERT(R), certified reference material

InChI=1/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H

The Henry's Law constant for acetophenone was measured as 1.04X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that acetophenone 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 61 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 32 days(SRC). Acetophenone's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Acetophenone is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.397 mm Hg(3).
Literature: (1) Betterton EA et al; Atmos Environ 25A: 1473-77 (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) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation Washington, DC: Taylor and Francis (1989)

The Koc of acetophenone was measured as 10, using an agricultural soil obtained from Northeastern China(1). According to a classification scheme(2), this Koc value suggests that acetophenone is expected to have very high mobility in soil(SRC).
Literature: (1) Ding Y, Wang L; Toxicol Environ Chem 78: 1-9 (2000) (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #The experimental and estimated log Koc for acetophenone in several soils and sediments ranged from 1.34-2.43(1-6,8). These values are indicative of medium to high mobility in soil and low adsorption to sediments(7).
Literature: (1) Bahnick DA, Doucette WJ; Chemosphere 17: 1703-15 (1988) (2) Sabljic A; Enviorn Sci Technol 21: 358-66 (1987) (3) Banwart WL et al; J Environ Sci Health B15: 165-79 (1980) (4) Hodson J, Williams NA; Chemosphere 17: 67-77 (1988) (5) Gerstl Z, Mingelgrin U; J Environ Sci Health B19: 297-312 (1984) (6) Khan A et al; Soil Sci 128: 297-302 (1979) (7) Swann RL et al; Res Rev 85: 17-28 (1983) (8) Southworth GR, Keller JL; Water Air Soil Poll 28: 239-48 (1986)

GEOSMIN

19700-21-1

(-)-geosmin

Octahydro-4alpha,8abeta-dimethyl-4aalpha(2H)-naphthol

MYW912WXJ4

CHEBI:46702

trans-1,10-dimethyl-trans-decalol

(4S-(4alpha,4aalpha,8abeta))-Octahydro-4,8a-dimethyl-4a(2H)-naphthol

(4S,4aS,8aR)-4,8a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalen-4a-ol

trans-1,10-Dimethyl-trans-9-decalol

(4S,4aS,8aR)-4,8a-dimethyloctahydronaphthalen-4a(2H)-ol

4a(2H)-Naphthalenol, octahydro-4,8a-dimethyl-, [4S-(4.alpha.,4a.alpha.,8a.beta.)]-

(4S,4aS,8aR)-4,8a-dimethyl-decahydronaphthalen-4a-ol

4a(2H)-Naphthalenol, octahydro-4,8a-dimethyl-,(4.alpha.,4a.alpha.,8a.beta.)-

(+/-)-Geosmin

1,10-Dimethyl-9-decalol

EINECS 243-239-8

UNII-MYW912WXJ4

rac Geosmin

4,8a-Dimethyloctahydro-4a(2H)-naphthalenol #

4,8alpha-dimethyl-octahydro-naphthalen-4alpha-ol

GEOSMIN [MI]

4,8A-DIMETHYLOCTAHYDRONAPHTHALEN-4A(2H)-OL

39 - Geosmin and MIB

SCHEMBL50009

4a-.alpha.-(2H)-Naphthol, octahydro-4-.alpha.,8a-.beta.-dimethyl-

CHEMBL2374043

FEMA NO. 4682

(4S,4aS,8aR)-Octahydro-4,8a-dimethyl-4a(2H)-naphthalenol

4a-alpha-(2H)-Naphthol, octahydro-4-alpha,8a-beta-dimethyl-

DTXSID801024112

4a(2H)-Naphthalenol, octahydro-4,8a-dimethyl-, (4S-(4-alpha,4a-alpha,8a-beta))-

NCGC00165950-01

(+/-)-Geosmin 10 microg/mL in Methanol

(+/-)-Geosmin 100 microg/mL in Methanol

NS00122563

Q420233

3-Methylanisole

100-84-5

1-Methoxy-3-methylbenzene

3-Methoxytoluene

m-Methylanisole

Benzene, 1-methoxy-3-methyl-

m-Cresol methyl ether

M-METHOXYTOLUENE

Anisole, m-methyl-

Methyl m-tolyl ether

m-Cresyl methyl ether

Methyl m-cresyl ether

3-Methylmethoxybenzene

Methyl 3-methylphenyl ether

1-Methyl-3-methoxybenzene

1-Methoxy-3-methyl-benzene

3-Methyl-1-methoxybenzene

NSC 6255

3-Cresol methyl ether

UI9I3Y6WTZ

CHEMBL349791

NSC-6255

META-CRESOL DEUTEROMETHYL ETHER

EINECS 202-893-4

UNII-UI9I3Y6WTZ

AI3-19476

m-Methyl anisole

3-methyl anisole

Meta-Methylanisole

3-methoxy toluene

3-Methylanisole, 99%

META METHOXYTOLUENE

SCHEMBL12353

DTXSID2051500

SCHEMBL12015250

AMY5179

NSC6255

CHEBI:167079

STR09347

BDBM50008537

MFCD00008395

AKOS000121157

MCULE-7649681864

DB-012728

CS-0034591

M0151

NS00005982

EN300-26366

H11854

A800280

W-108936

Q27291091

Z53834440

F0001-0028

InChI=1/C8H10O/c1-7-4-3-5-8(6-7)9-2/h3-6H,1-2H

ETHYL OCTANOATE

Ethyl caprylate

106-32-1

Ethyl n-octanoate

Caprylic acid ethyl ester

Octanoic acid, ethyl ester

Ethyl octoate

Ethyl octylate

octanoic acid ethyl ester

FEMA No. 2449

n-Octanoic Acid Ethyl Ester

Octanoic acid-ethyl ester

MFCD00009552

n-Caprylic acid ethyl ester

DTXSID8051542

81C5MOP582

NSC-8898

WE(2:0/8:0)

Ethyl octanoate (natural)

Caprylic acid ethylester

NSC 8898

EINECS 203-385-5

BRN 1754470

ethyloctanoate

UNII-81C5MOP582

AI3-01977

Ethyl ester octanoic acid

SCHEMBL454

Ethyl ester of octanoic acid

ETHYL CAPRYLATE [MI]

WLN: 7VO2

ETHYL OCTANOATE [FCC]

ETHYL OCTANOATE [FHFI]

CHEMBL4633100

DTXCID9030094

CHEBI:87426

FEMA 2449

NSC8898

Tox21_303730

LMFA07010447

AKOS000120258

Ethyl octanoate, >=98%, FCC, FG

CS-W016021

HY-W015305

MCULE-2970505348

NCGC00357039-01

CAS-106-32-1

LS-13892

Ethyl octanoate, ReagentPlus(R), >=99%

DB-040685

Octanoic acid ethyl ester (ethyl octanoate)

NS00012443

O0030

EN300-21302

Ethyl octanoate, analytical reference material

Ethyl octanoate, natural, >=98%, FCC, FG

Ethyl octanoate, Vetec(TM) reagent grade, 98%

A801420

J-001572

Q3348790

2-HEXANOL

hexan-2-ol

626-93-7

2-Hydroxyhexane

2-Hexyl Alcohol

(+/-)-2-Hexanol

Butyl methyl carbinol

n-C4H9CH(OH)CH3

9CDT0V6T4P

54972-97-3

CHEBI:88370

Methylamyl alcohol

NSC-3706

MFCD00004585

2-Hexanol, (R)-

2-Hexanol, (S)-

69203-06-1

sec-Hexanol

s-(+)-2-hexanol

Pentanol, methyl-

n-Butylmethylcarbinol

1-Pentanol, methyl-

NSC 3706

EINECS 210-971-4

BRN 1718996

2-aHexanol

n-Hexan-2-ol

Hexanol-(2)

(RS)-2-hexanol

2-Hexanol, 99%

METHYLBUTYLCARBINOL

Hexan-2-ol; 2-Hexanol

DL-HEXAN-2-OL

UNII-9CDT0V6T4P

2-Hexanol, >=98%

SCHEMBL15074

37769-60-1

4-01-00-01708 (Beilstein Handbook Reference)

CHEMBL45425

1-PENTANOL , METHYL-

2-Hexanol, analytical standard

2-Hexanol, (.+/-.)-

DTXSID30893088

NSC3706

LMFA05000467

AKOS009156480

(+/-)-1-METHYL-1-PENTANOL

MCULE-6558228722

BS-22913

DB-016694

DB-323114

H0131

NS00012563

EN300-107421

Q77003

20281-86-1

1-OCTEN-3-OL

3391-86-4

Oct-1-en-3-ol

1-Vinylhexanol

Vinyl amyl carbinol

3-Hydroxy-1-octene

Amyl vinyl carbinol

Mushroom alcohol

Pentyl vinyl carbinol

Octen-3-ol

Matsuica alcohol

Vinyl hexanol

Pentylvinylcarbinol

octene-1-ol-3

Oct-1-ene-3-ol

(+/-)-1-octen-3-ol

Matsutake alcohol

1-Okten-3-ol

FEMA No. 2805

n-Oct-1-en-3-ol

NSC 87563

(R)-1-octen-3-ol

WXB511GE38

DTXSID3035214

CHEBI:34118

MFCD00004589

NSC-87563

Amylvinylcarbinol

Morrilol

1-Okten-3-ol [Czech]

1-Octen-3-ol (natural)

Matsutake alcohol [Japanese]

1-Octene-3-ol

dl-1-Octen-3-ol

EINECS 222-226-0

EPA Pesticide Chemical Code 069037

BRN 1744110

UNII-WXB511GE38

Morillol

AI3-28627

CCRIS 8804

Matsuika alcohol

MOGUCHUN

Vinyl pentyl carbinol

(E)-1-octen-3-ol

Flowtron mosquito attractant

SCHEMBL41968

1-Octen-3-ol, 98%

WLN: QY5&1U1

CHEMBL3183573

DTXCID1015214

1-OCTEN-3-OL [FCC]

1-OCTEN-3-OL [FHFI]

1-Octen-3-ol, analytical standard

BCP19092

NSC87563

Tox21_302039

LMFA05000090

LMFA05000712

AKOS009157412

CS-W011126

DS-8600

NCGC00255686-01

1-Octen-3-ol, >=98%, FCC, FG

1-Octen-3-ol, natural, >=95%, FG

PD042153

CAS-3391-86-4

DB-003193

NS00004677

O0159

1-Octen-3-ol stabilized with alpha-tocopherol

4-(Trifluoromethyl)-2-biphenyl-carboxylic acid

D91822

EN300-6981750

A821997

Q161667

Q-100412