Palmitelaidic acid methyl ester

Methyl cis-9-hexadecenoate

methyl hexadec-9-enoate

AC1L23G5

CTK0I2512

CTK1B4279

9-Hexadecenoic acid, methyl ester

LP087515

ACMC-2099c6

ANW-16372

TRA0091388

AKOS025243510

methyl (E)-hexadec-9-enoate

10030-74-7

9-hexadecenoic acid, methyl ester, (9Z)-

Methyl hexadecanoate

formyl hexadecanoate

FLIACVVOZYBSBS-UHFFFAOYSA-N

METHYL PALMITATE

Methyl n-hexadecanoate

Hexadecanoic acid methyl ester

Methyl palmitate, analytical standard

AC1Q5ZZN

Palmitic acid methyl ester

n-Hexadecanoic acid methyl ester

DPY8VCM98I

Hexadecanoic acid, methyl ester

AC1L1QG4

Uniphat A60

UNII-DPY8VCM98I

Palmitic acid, methyl ester

KSC492E9B

Methyl palmitate, >=97%

NSC4197

SCHEMBL37365

2178AA

Metholene 2216

P0006

CTK3J2290

S0311

CHEMBL335125

ACMC-2099em

Emery 2216

C16995

Radia 7120

HSDB 5570

HMS3650G09

Methyl palmitate, United States Pharmacopeia (USP) Reference Standard

Jsp000954

NSC 4197

NSC-4197

LP002416

SBB060596

STL146153

Hexadecanoic acid methyl ester (FAME MIX)

BBL010507

CS-D1457

AK114523

DTXSID4029149

CHEBI:69187

DSSTox_CID_9149

AX8139568

ANW-16460

CC-30788

AN-22697

SC-19066

DSSTox_GSID_29149

DSSTox_RID_78683

BB_NC-2294

C-28202

ZINC43871947

LMFA07010470

MFCD00008994

DB-041084

LS-178760

AI3-03509

TR-002423

KB-257908

ST51046747

ST24031200

RTR-002423

AKOS005715213

J-002763

FT-0628772

I14-13858

Palmitic acid, methyl ester (8CI)

Methyl palmitate, >=99% (capillary GC)

EiO notEa(1/4)xo yen

Tox21_202768

Methyl hexadecanoate, 97% 100g

112-39-0

NCGC00260315-01

MCULE-2282587787

CAS-112-39-0

E(R)AuEa(1/4)xo yen

EINECS 203-966-3

MolPort-001-780-242

WE(1:0/16:0)

844D5088-5CCF-4B2D-A678-EA5A7E8CB149

The Henry's Law constant for methyl palmitate is estimated as 0.009 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that methyl palmitate 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 approximately 5 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 6.5 days(SRC). Methyl palmitate's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). The volatilization half-life from a model pond 2 m deep is estimated to be about 60 hours ignoring adsorption; when considering maximum adsorption the volatilization half-life increases to 150 days(3). Methyl palmitate is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.00006 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) Perry RH, Green D; Perry's Chemical Engineer's Handbook. Physical and Chemical Data. NY,NY: McGraw-Hill 6th ed (1984)

Insol in water; very sol in ethyl alc, acetone; sol in ether
Literature: Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 76th ed. Boca Raton, FL: CRC Press Inc., 1995-1996., p. 3-184
Literature: #Insoluble in water, soluble in alcohol and ether
Literature: Lewis, R.J., Sr (Ed.). Hawley's Condensed Chemical Dictionary. 12th ed. New York, NY: Van Nostrand Rheinhold Co., 1993, p. 776

Using a structure estimation method based on molecular connectivity indices(1), the Koc for methyl palmitate can be estimated to be about 18,000(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl palmitate is expected to be immobile 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)

Methylcinnamate

CCRCUPLGCSFEDV-BQYQJAHWSA-N

Methyl cinnamylate

Methyl cinnamate

methyl-cinnamate

Benzeneacrylic acid methyl ester

methyl trans cinnamate

Methyl trans-cinnamate

trans-Methyl cinnamate

Cinnamic acid methyl

Methyl 3-phenylpropenoate

Methyl cinnamate, analytical reference material

Methyl 3-phenylacrylate

AC1LCUE5

AC1Q5YZH

Cinnamic acid methyl ester

Methyl trans-cinnamate, analytical standard

Methyl trans-3-Phenylacrylate

trans-Cinnamic acid methyl ester

Methyl 3-phenyl propenoate

Nat. Methyl Cinnamate

AC1Q41KG

533CV2ZCQL

CINNAMIC ACID, METHYL ESTER

Methyl cinnamate (natural)

PubChem8189

A517

trans-3-Phenylacrylic Acid Methyl Ester

CHEMBL55060

NSC9411

UNII-533CV2ZCQL

(E)-Methyl cinnamate

Methyl (E)-cinnamate

SemaSORB 9815

EBD44996

Methyl 3-phenyl-2-propenoate

methyl-3 phenylprop-2-enoate

methyl-3-phenylprop-2-enoate

RP17386

SCHEMBL101530

C06358

CHEBI:6857

Methyl trans-cinnamate, 99%

ZINC896129

AK312789

DTXSID5044314

LS-2916

Methyl (E)-3-phenylpropenoate

Methyl trans-3-phenyl-2-propenoate

NSC 9411

NSC-9411

OR025160

OR231744

SBB058222

TL806143

trans-Methyl 3-Phenyl-2-propenoate

WLN: 1OV1U1R

ZB015073

3-Phenyl-2-propenoic acid methyl

Methyl cinnamate, (E)

3-Phenyl-2-propenoic acid methyl ester

AJ-24225

AK-93451

AN-24625

DSSTox_GSID_44314

Methyl (2E)-3-phenylpropenoate

DSSTox_CID_22151

DSSTox_RID_80147

Methyl (2E)-3-phenylacrylate

MFCD00008458

ZINC00896129

AI3-00579

KB-203137

RTR-030565

ST24031190

ST50411952

TC-166123

TR-030565

trans-3-Phenyl-2-propenoic acid methyl ester

(E)-3-Phenylacrylic acid methyl ester

AKOS015890136

ghl.PD_Mitscher_leg0.369

I01-5731

I01-7774

J-000917

J-011115

J-522598

Q-100258

FEMA No. 2698

FT-0623832

Tox21_301384

103-26-4

Methyl (E)-3-phenyl-2-propenoate

Methyl (E)-3-phenylprop-2-enoate

1754-62-7

Methyl cinnamate, 99% 100g

Methyl trans-cinnamate, >=98%, FCC, FG

NCGC00255910-01

EINECS 203-093-8

methyl (2E)-3-phenylprop-2-enoate

Cinnamic acid, methyl ester, (E)-

Methyl 3-phenyl propenoate; 3-Phenyl-2-propenoic acid methyl ester

Methyl cinnamate, >=99.0% (GC)

(E)-3-Phenyl-2-propenoic acid methyl ester

CAS-1754-62-7

Methyl cinnamate, natural, >=98%, FCC, FG

403649-70-7

925685-28-5

Methyl (2E)-3-phenyl-2-propenoate #

(2E)-3-Phenyl-2-propenoic acid methyl ester

MolPort-001-783-139

MolPort-019-640-936

2-PROPENOIC ACID, 3-PHENYL-, METHYL ESTER, (E)-

2-propenoic acid, 3-phenyl-, methyl ester, (2E)-

InChI=1/C10H10O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-8H,1H3/b8-7

Methyl 9-octadecenoate

AC1L1QHV

Methyl cis-9-octadecenoate

9-Octadecenoic acid,methyl ester

KSC492C0P

ACMC-209exc

CTK4F4070

CTK4E1349

CTK3J2107

ACMC-209t6b

Emerest 2301

LP106947

ANW-42081

ANW-23614

AN-22713

AN-22224

(Z)-9-Octadecenoic acid methyl ester

AKOS030228845

MCULE-8140747078

2462-84-2

EINECS 219-559-9

9-Octadecenoic acid, methyl ester, (9E)-

The Henry's Law constant for methyl oleate is estimated as 0.014 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that methyl oleate 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 approximately 5 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 7 days(SRC). The volatilization half-life from a model pond 2 m deep is estimated to be about 61 hours ignoring adsorption; when considering maximum adsorption the volatilization half-life increases to 18 months(3). Methyl oleate's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). Methyl oleate is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 6.3X10-6 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 (1989)

Insol in water; miscible with ethyl alcohol, ether; sol in chloroform
Literature: Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 76th ed. Boca Raton, FL: CRC Press Inc., 1995-1996., p. 3-228

Using a structure estimation method based on molecular connectivity indices(1), the Koc for methyl oleate can be estimated to be about 62,000(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl oleate is expected to be immobile 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)

Dimethyloxalate

dimethyl ethanedioate

LOMVENUNSWAXEN-UHFFFAOYSA-N

Dimethyl oxalate

METHYL OXALATE

dimethyl oxalate radical cation

Oxalic acid dimethyl

AC1L1WNT

Oxalic acid dimethyl ester

Ethanedioic acid, dimethyl ester

AC1Q41NE

SCHEMBL8295

Oxalic acid, dimethyl ester

KSC492I1J

Methyl oxalate; Oxalic acid dimethyl ester

NSC9374

ACMC-209lmq

O0080

CTK3J2414

NE10581

RP19293

dimethyl ethane-1,2-dioate

CHEBI:6859

C10900

IQ3Q79344S

Ethanedioicacid, 1,2-dimethyl ester

SBB040902

NSC-9374

NSC 9374

OR025041

DTXSID9060287

STL146620

BBL011507

ZINC1532047

A830619

UNII-IQ3Q79344S

SC-81002

CJ-24113

CJ-05237

ANW-32304

AN-23672

LS-99429

AB1003115

TRA0001393

Ethanedioic acid, 1,2-dimethyl ester

MFCD00008442

BB_SC-7155

ST50214504

RTR-019525

KB-251654

TR-019525

AI3-21214

S01-0414

AKOS000269022

Q-200995

FT-0625150

Dimethyl oxalate, ReagentPlus(R), 99%

EN300-20093

F0001-1452

553-90-2

MCULE-5018268642

EINECS 209-053-6

Dimethyl oxalate, Vetec(TM) reagent grade, 98%

MolPort-000-872-065

132425-EP2269990A1

132425-EP2295425A1

132425-EP2287157A1

InChI=1/C4H6O4/c1-7-3(5)4(6)8-2/h1-2H