myricetin

529-44-2

Cannabiscetin

Myricetol

Myricitin

3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one

3,3',4',5,5',7-Hexahydroxyflavone

3,5,7,3',4',5'-Hexahydroxyflavone

3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

delphidenolon 1575

3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one

CCRIS 5838

NSC 407290

NSC-407290

4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-

UNII-76XC01FTOJ

EINECS 208-463-2

76XC01FTOJ

3,3',4,4',5',7-Hexahydro-2-phenyl-4H-chromen-4-one

BRN 0332331

CHEBI:18152

HSDB 7682

MFCD00006827

NSC407290

CHEMBL164

FLAVONE, 3,3',4',5,5',7-HEXAHYDROXY-

Myricetin from Myrica cerifera leaf and bark

SMR001233193

SR-01000076005

Myrc

4gqr

C15H10O8

Prestwick_342

Spectrum_001501

SpecPlus_000531

MYRICETIN [MI]

MYRICETIN [HSDB]

MYRICETIN [INCI]

Prestwick0_000465

Prestwick1_000465

Prestwick2_000465

Prestwick3_000465

Spectrum4_001272

Spectrum5_000692

Lopac-M-6760

Myricetin (Cannabiscetin)

BIDD:PXR0079

Lopac0_000740

SCHEMBL19302

BSPBio_000570

KBioGR_001884

KBioSS_001981

MLS002153825

MLS006010718

BIDD:ER0142

DivK1c_006627

Myricetin, analytical standard

SPBio_002509

BPBio1_000628

MEGxp0_000357

DTXSID8022400

ACon1_000267

BDBM15236

cid_5281672

GTPL13074

KBio1_001571

KBio2_001981

KBio2_004549

KBio2_007117

2o63

CHEBI: 18152

REGID_for_CID_5281672

HMS1569M12

HMS2096M12

HMS2231L04

HMS3262C22

HMS3656I05

Myricetin - CAS 529-44-2

BCP28295

Myricetin, >=96.0% (HPLC)

Myricetin, >=96.0%, crystalline

TNP00286

Tox21_500740

HB0434

LMPK12110001

s2326

STL284709

3,7,3',4',5'-Hexahydroxyflavone

AKOS015903103

AC-4533

CCG-204825

CS-6221

DB02375

KS-5268

LP00740

MCULE-6299186219

SDCCGSBI-0050718.P003

3,3',4',5,5',7-hexOH-Flavone

Flavone,3',4',5,5',7-hexahydroxy-

NCGC00015697-01

NCGC00015697-02

NCGC00015697-03

NCGC00015697-04

NCGC00015697-05

NCGC00015697-06

NCGC00015697-07

NCGC00015697-08

NCGC00015697-09

NCGC00015697-10

NCGC00015697-11

NCGC00015697-12

NCGC00015697-13

NCGC00015697-14

NCGC00015697-25

NCGC00094083-01

NCGC00094083-02

NCGC00094083-03

NCGC00094083-04

NCGC00179517-01

NCGC00179517-02

NCGC00261425-01

CAS-529-44-2

HY-15097

NCI60_003870

SY051702

EU-0100740

M2131

NS00014642

SW196616-2

M 6760

S00115

3,3',4',5,5',7-hexahydroxy-(8CI)- flavone

A829320

Q951449

C07E0ED2-ABF6-4BD3-A2B2-A98CAEF20FD1

Myricetin, primary pharmaceutical reference standard

Q-100601

SR-01000076005-1

SR-01000076005-6

BRD-K43149758-001-04-5

3,3′,4′,5,5′,7-Hexahydroxyflavone

Cannabiscetin; HSDB 7682; HSDB7682; HSDB-7682

3,4,5-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-7-one

3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one #

4H-1-Benzopyran-4-one,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-

Sparingly soluble in boiling water; soluble in alcohol. Practically insoluble in chloroform, acetic acid
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 2006., p. 1095
Literature: #In water, 54.9 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from, as of Feb 4, 2009: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm

pyrogallol

benzene-1,2,3-triol

87-66-1

1,2,3-trihydroxybenzene

pyrogallic acid

1,2,3-benzenetriol

fourrine PG

Fouramine Brown AP

fourrine 85

Pyro

Piral

C.I. Oxidation Base 32

fouramine base ap

C.I. 76515

1,2,3-Trihydroxybenzen

CI Oxidation Base 32

Benzene, 1,2,3-trihydroxy-

NSC 5035

2,3-Dihydroxyphenol

CCRIS 1940

HSDB 794

NSC-5035

EINECS 201-762-9

UNII-01Y4A2QXY0

BRN 0907431

01Y4A2QXY0

CI 76515

DTXSID6025983

CHEBI:16164

AI3-00709

1,2,3-Trihydroxybenzen [Czech]

1,2,3-TRIHYDROXY-BENZENE

benzene-1,2-3-triol

CHEMBL307145

DTXCID905983

4-06-00-07327 (Beilstein Handbook Reference)

Benzene-1,2,3-triol (Pyrogallol)

MFCD00002192

NCGC00091507-01

PYROGALLOL (MART.)

PYROGALLOL [MART.]

1,2,3-Trihydroxybenzen (CZECH)

acid, Pyrogallic

CAS-87-66-1

Pyrogallol [NF]

PYG

PYROGALLOL, ACS

Pyrogallic

Pyrogallol;

trihydroxybenzene

1,3-Benzenetriol

Pyrogallol, 98%

PYROP

Pyrogallol ACS grade

1,3-Trihydroxybenzen

Pyrogallic Acid,(S)

1,3-Trihydroxybenzene

PYROGALLOL [MI]

Pyrogallol, ACS reagent

PYROGALLOL [HSDB]

PYROGALLOL [INCI]

Benzene,2,3-trihydroxy-

WLN: QR BQ CQ

PYROGALLOL [VANDF]

SCHEMBL3532

PYROGALLOL [WHO-DD]

C.I. Oxidation Base 32

MLS001066376

Pyrogallol, analytical standard

1,2,3-Trihydroxybenzene, XIV

Pyrogallol, >=98% (HPLC)

Pyrogallol, p.a., ACS reagent

NSC5035

BCP15871

HY-N1579

Pyrogallol, ACS reagent, >=99%

STR08708

Tox21_111143

Tox21_202373

BBL011607

BDBM50031472

Pyrogallol, Vetec(TM) reagent grade

s3885

STL163335

AKOS000120163

AM10660

CCG-266100

CS-W019928

MCULE-6282052463

1,2,3-Benzenetriol (ACD/Name 4.0)

NCGC00091507-02

NCGC00091507-03

NCGC00259922-01

Pyrogallol, purum, >=98.0% (HPLC)

AC-11384

BP-12538

DA-40956

GMN

Pyrogallol, SAJ first grade, >=98.0%

SMR000471842

Pyrogallol, JIS special grade, >=99.0%

NS00014915

P0570

EN300-18055

A15863

C01108

AB-131/40221933

Q388692

W-104009

Z57127553

2,3-Dihydroxyphenol; Benzene-1,2,3-triol; NSC 5035

F0001-2163

InChI=1/C6H6O3/c7-4-2-1-3-5(8)6(4)9/h1-3,7-9

30813-84-4

The Henry's Law constant for pyrogallic acid is estimated as 1.57X10-10 atm-cu m/mole(SRC) derived from its vapor pressure, 4.79X10-4 mm Hg(1), and water solubility, 5.07X10+5 mg/L(2). This Henry's Law constant indicates that the neutral species of pyrogallic acid is expected to be essentially nonvolatile from water surfaces(3). The pKa of pyrogallic acid is 9.01(4), indicating that this compound will partially exist in the anion form in the environment, and anions do not volatilize(SRC). Pyrogallic acid is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Yaws CL; Handbook of Vapor Pressure. Vol 3: C8-C28 Compounds. Houston, TX: Gulf Pub Co (1994) (2) Yalkowsky SH, He Y, eds; Handbook of aqueous solubility data. Boca Raton, FL: CRC Press p. 260 (2003) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) Kortum G et al; Dissociation Constants of Organic Acids in Aqueous Solution. International Union of Pure and Applied Chemistry. London: Butterworth (1961)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of pyrogallic acid can be estimated to be 320(SRC). According to a classification scheme(2), this estimated Koc value suggests that pyrogallic acid is expected to have moderate mobility in soil. The pKa of pyrogallic acid is 9.01(3), indicating that this compound will partially exist in the anion form in the environment and anions do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4).
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from, as of April 12, 2010: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Kortum G et al; Dissociation Constants of Organic Acids in Aqueous Solution. International Union of Pure and Applied Chemistry. London: Butterworth (1961) (4) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

p-coumaric acid

4-Hydroxycinnamic acid

501-98-4

p-Hydroxycinnamic acid

trans-4-Hydroxycinnamic acid

7400-08-0

4-Coumaric acid

trans-p-Coumaric acid

p-Cumaric acid

3-(4-hydroxyphenyl)acrylic acid

p-Hydroxy-cinnamic acid

Para-Coumaric acid

Naringeninic acid

Hydroxycinnamic acid

(E)-p-Coumaric acid

trans-4-coumaric acid

trans-p-Coumarinic acid

(E)-3-(4-Hydroxyphenyl)acrylic acid

Cinnamic acid, p-hydroxy-

(E)-p-Hydroxycinnamic acid

2-propenoic acid, 3-(4-hydroxyphenyl)-, (2E)-

4'-hydroxycinnamic acid

trans-p-Hydroxycinnamic acid

p-Hydroxyphenylacrylic acid

(2E)-3-(4-hydroxyphenyl)prop-2-enoic acid

3-(4-Hydroxyphenyl)-2-propenoic acid

4-coumarate

Cinnamic acid, p-hydroxy-, (E)-

trans-p-Hydroxycinnamate

2-Propenoic acid, 3-(4-hydroxyphenyl)-

(E)-3-(4-Hydroxyphenyl)-2-propenoic acid

(E)-3-(4-hydroxyphenyl)prop-2-enoic acid

4-Hydroxycinnamate

(2E)-3-(4-hydroxyphenyl)acrylic acid

beta-(4-Hydroxyphenyl)acrylic acid

NSC 59260

trans-4-hydroxycinnamate

UNII-IBS9D1EU3J

IBS9D1EU3J

EINECS 231-000-0

Para coumaric acid

(E)-4-hydroxycinnamic acid

3-(4-hydroxyphenyl)prop-2-enoic acid

NSC 674321

p-coumarate

2-Propenoic acid, 3-(4-hydroxyphenyl)-, (E)-

BRN 2207381

BRN 2207383

CHEBI:32374

ORISTAR PCA

parahydroxycinnamic acid

MFCD00004399

NSC-59260

NSC-674321

4-hydroxy cinnamic acid

CHEMBL66879

PARA HYDROXYCINNAMIC ACID

beta-[4-Hydroxyphenyl]acrylic acid

0-10-00-00297 (Beilstein Handbook Reference)

4-10-00-01005 (Beilstein Handbook Reference)

NSC674321

trans-p-coumarate

Dehydroepiandrosterone-[D6] (CertiMass solution)

3-(4-hydroxyphenyl)acrylate

.beta.-[4-Hydroxyphenyl]acrylic acid

trans-HPPA

(E)-3-[4-hydroxyphenyl]-2-propenoic acid

4-coumaric acid, (E)-isomer

4-Hydroxycinnamicacid

trans-p-Cumaric Acid

4-Hydroxycinamic acid

.BETA.-(4-HYDROXYPHENYL)ACRYLIC ACID

2-Propenoic acid, 3-(4-hydroxyphenyl)-, (Z)-

CHEBI:36090

hydroxycinnamate

Para coumarate

p-coumaric-acid

Para-Coumarate

p-Cumarate

naringeninic-acid

p-Hydroxycinnamate

4qem

Coumaric acid, p-

4'-Hydroxycinnamate

4-Hydroxy cinnamate

p-Coumaric acid,trans

p-Coumaric acid 98%

4f8j

p-Coumaric acid, trans

4-Hydroxyphenylpropenoate

(2E)-3-(4-Hydroxyphenyl)-2-propenoic acid

trans-3-(4'-hydroxyphenyl)-2-propenoic acid

bmse000150

bmse000591

bmse010208

trans-4-HydroxycinnamicAcid

b-[4-Hydroxyphenyl]acrylate

SCHEMBL39106

p-hydroxycinnamic acid (M4)

MLS001066419

p-Hydroxycinnamic acid, trans

P-COUMARIC ACID [MI]

beta-[4-Hydroxyphenyl]acrylate

BDBM4374

GTPL5787

SODIUM2,4-PENTANEDIONATE

b-[4-Hydroxyphenyl]acrylic acid

trans-p-HydroxyzimtsA currencyure

DTXSID30901076

P-COUMARIC ACID [WHO-DD]

HMS1409E10

3-(4-Hydroxyphenyl)-2-propenoate

HYDROXYCINNAMIC ACID [INCI]

BCP22803

HY-N2391

NSC59260

STR06515

4-HYDROXYPHENYLPROPENOIC ACID

Cinnamic acid, 4-hydroxy-, trans-

AC7957

BBL012226

CK2547

s4759

s9564

STL163567

AKOS000120685

p-Coumaric acid;p-Hydroxycinnamic acid

BCP9001042

CCG-266309

CS-W020394

DB04066

p-Coumaric acid, >=98.0% (HPLC)

(E)-3-(4-hydroxyphenyl)prop-2-enoate

NCGC00246974-01

1ST40051

50940-26-6

AC-10318

AC-34130

AC-34133

AS-12000

BP-13278

SMR000112201

(E)-3-(4-hydroxyphenyl)prop-2-enoicacid

trans-p-Coumaric acid, analytical standard

AM20050138

NS00068187

EN300-17292

A19490

C00811

Q99374

(2E)-3-(4-Hydroxyphenyl)-2-propenoic acid #

A828008

AE-562/40414679

trans-p-Coumaric acid 1000 microg/mL in Acetone

Q-100560

W-104438

Z56911963

0C1BFF2D-2CF7-4FC1-9F76-3268C2C7F783

F2191-0188

p-Coumaric acid, primary pharmaceutical reference standard

(E)-3-(4-hydroxyphenyl)prop-2-enoate;Trans-4-Hydroxycinnamic Acid

InChI=1/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)/b6-3

Gallic acid

3,4,5-Trihydroxybenzoic acid

149-91-7

gallate

Benzoic acid, 3,4,5-trihydroxy-

Gallic acid, tech.

Kyselina gallova

Pyrogallol-5-carboxylic acid

GALOP

HSDB 2117

CCRIS 5523

3,4,5-Trihydroxybenzoate

MFCD00002510

NSC 674319

CHEBI:30778

Kyselina 3,4,5-trihydroxybenzoova

AI3-16412

EINECS 205-749-9

NSC 20103

NSC-20103

NSC-674319

UNII-632XD903SP

BRN 2050274

DTXSID0020650

632XD903SP

NSC20103

3,4,5-Trihydroxybenzoic acid, anhydrous

DTXCID60650

CHEMBL288114

3,4,5-trihydroxy-Benzoic acid

3-10-00-02070 (Beilstein Handbook Reference)

NSC674319

NCGC00091125-01

GALLIC ACID ANHYDROUS

Kyselina gallova [Czech]

Acid, Gallic

CAS-149-91-7

Gallic acid [NF]

SR-05000001537

gallic-acid

Kyselina 3,4,5-trihydroxybenzoova [Czech]

Gallic acid tech.

Gallic Acid, F

GDE

Gallic Acid1520

Spectrum_000342

SpecPlus_000307

5-Trihydroxybenzoic acid

Spectrum2_000399

Spectrum3_000254

Spectrum4_001544

Spectrum5_000108

GALLIC ACID [MI]

bmse000389

3,5-Trihydroxybenzoic acid

GALLIC ACID [HSDB]

GALLIC ACID [INCI]

3,4,5-hydroxybenzoic acid

WLN: QVR CQ DQ EQ

3,4,5-trihydroxy-Benzoate

Oprea1_087792

SCHEMBL15012

3,4,5-Trihydroxybenzoicacid

BSPBio_001668

KBioGR_002008

KBioSS_000822

SPECTRUM210369

65271-60-5

BIDD:ER0374

DivK1c_006403

GALLIC ACID [WHO-DD]

SPBio_000617

3,4,5-Trihydroxybenzoate, X

Benzoic acid,4,5-trihydroxy-

GTPL5549

3,4,5-Trihydroxybenzoic acid;

KBio1_001347

KBio2_000822

KBio2_003390

KBio2_005958

KBio3_001168

CPD-183

DTXSID50420476

Gallic acid, puriss., 98.0%

1,5-Cyclohexadiene-1-carboxylic acid, 5-hydroxy-3,4-dioxo-

HMS1923K07

HMS2091A07

Pharmakon1600-00210369

BCP18127

HY-N0523

NSC36997

Tox21_111089

Tox21_202515

BBL009937

BDBM50085536

CCG-38670

NSC-36997

NSC755825

s4603

STK298718

AKOS000119625

Tox21_111089_1

AC-1206

CS-8191

MCULE-1552954312

NSC-755825

PS-8710

SDCCGMLS-0066503.P001

NCGC00091125-02

NCGC00091125-03

NCGC00091125-04

NCGC00091125-05

NCGC00091125-07

NCGC00091125-13

NCGC00260064-01

DA-33612

SY038078

SBI-0052184.P002

Gallic acid, 97.5-102.5% (titration)

G0011

NS00013682

EN300-21542

C01424

D85056

3,4,5-trihydroxybenzoic acid (ACD/Name 4.0)

AB00052697_03

Q375837

Q-201146

SR-05000001537-1

SR-05000001537-2

SR-05000001537-3

BRD-K77345217-001-01-9

F1908-0156

Gallic acid, certified reference material, TraceCERT(R)

Z104501122

78563C7D-0E2D-4766-A8EA-670A03C78FCF

GALLIC ACID (CONSTITUENT OF GRAPE SEEDS OLIGOMERIC PROANTHOCYANIDINS)

InChI=1/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12

137657-43-3

The Henry's Law constant for gallic acid is estimated as 8.5X10-20 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This value indicates that gallic acid will be essentially nonvolatile from water surfaces(2,SRC). Gallic acid's Henry's Law constant(1,SRC) indicates that volatilization from moist soil surfaces is not expected(SRC). Gallic acid is not expected to volatilize from dry soil surfaces based on an estimated vapor pressure of 1.2X10-7 mm Hg(SRC), determined from a fragment constant method(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) Lyman WJ; p 31 in Environmental Exposure From Chemicals Vol I, Neely WB, Blau GE(eds), Boca Raton, FL: CRC Press (1985)

The Koc of gallic acid is estimated as approximately 57(SRC), using a measured log Kow of 0.70(1) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that gallic acid 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. Washington, DC: American Chemical Society (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: 23 (1983)

naringin

10236-47-2

aurantiin

Naringoside

Naringenin 7-Rhamnoglucoside

(2S)-Naringin

Naringenin 7-O-neohesperidoside

UNII-N7TD9J649B

N7TD9J649B

CHEBI:28819

Naringenine-7-rhamnosidoglucoside

Naringenin-7-beta-neohesperidoside

EINECS 233-566-4

4'5-diOH-Flavone-7-rhgluc

AI3-19008

CHEMBL451532

7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihyd

DTXSID6022478

NARINGENIN-7-RHAMNOGLUCOSIDE

(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2

(S)-7-(((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy

4',5,7-Trihydroxyflavanone-7-rhamnoglucoside

NARINGIN (USP-RS)

NARINGIN [USP-RS]

5-Hydroxy-2-(4-hydroxyphenyl)-7-(2-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyloxy)-4-chromanon

7-(2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyloxy)-2,3-dihydro-4',5,7-trihydroxyflavone

4',5,7-trihydroxyflavanone 7-rhamnoglucoside

Naringenin 7-O-alpha-L-rhamnosyl-(1->2)-beta-D-glucoside

naringenin 7-O-(alpha-L-rhamnosyl-(1,2)-beta-D-glucoside)

Naringenin 7-O-[alpha-L-rhamnosyl-(1->2)-beta-D-glucoside]

MFCD00148888

(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside

(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside

4H-1-Benzopyran-4-one, 7-((2-O-(6-deoxy-alpha-L-mannapyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl), (S)-

SR-01000736681

naringenin-7-hesperidoside

Naringenin 7-O-(alpha-L-rhamnosyl-(1->2)-beta-D-glucoside)

Naringin extract

Naringenin,(S)

(S)-7-((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)tetrahydro-2H-pyran-2-yloxy)-5-

Naringenin Glycoside

Naringin (Naringoside)

NARINGIN [INCI]

NARINGIN [MI]

132203-74-8

Prestwick0_000467

Prestwick1_000467

Prestwick2_000467

Prestwick3_000467

AURANTIIN [WHO-DD]

SCHEMBL23432

BSPBio_000574

cid_25075

MLS000069459

BIDD:ER0262

DivK1c_000247

SPBio_002513

BPBio1_000632

cid_442428

DTXCID302478

GTPL4738

MEGxp0_001877

ACon1_000139

HMS500M09

KBio1_000247

NINDS_000247

CITRUS NARINGININE [VANDF]

HMS2231M18

HY-N0153

BDBM50241582

s2329

AKOS016034302

CCG-208591

CS-5632

MCULE-5348711723

IDI1_000247

NCGC00142617-01

NCGC00142617-02

NCGC00142617-03

1ST40036

AS-12929

SMR000059108

XN167836

NS00014639

C09789

A800566

Q418469

SR-01000736681-4

SR-01000736681-5

BRD-K02953697-001-09-2

BRD-K02953697-002-03-3

(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-betaD-glucopyranoside

(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-5-hydro

(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)ch

(2S)-7-[(2S,4S,5S,3R,6R)-3-((2S,6S,3R,4R,5R)-3,4,5-trihydroxy-6-methyl(2H-3,4, 5,6-tetrahydropyran-2-yloxy))-4,5-dihydroxy-6-(hydroxymethyl)(2H-3,4,5,6-tetra hy

(2S)-7-{[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-5-hydroxy-2-(4-hydroxypheny

(S)-7-((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydro-2H-pyran-2-yloxy)-tetrahydro-2H-pyran-2-yloxy)-

4H-1-Benzopyran-4-one, 7-((2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)-

4H-1-Benzopyran-4-one,7-[[2-O-(6-deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-,(S)-

7-((2-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSYL)OXY)-2,3-DIHYDRO-5-HYDROXY-2-(4-HYDROXYPHENYL)-4H-1-BENZOPYRAN-4-ONE

7-[[2-O-(6-Deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl]oxy]-5-hydroxy-2(S)-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

ZWN

ISOVALERIC ACID

3-Methylbutanoic acid

503-74-2

Isopentanoic acid

3-Methylbutyric acid

Delphinic acid

Isopropylacetic acid

Isovalerianic acid

Butanoic acid, 3-methyl-

Isobutylformic acid

Isovalerianic

beta-Methylbutyric acid

Acetic acid, isopropyl-

3-Methylbutyrate

Butyric acid, 3-methyl-

3-methyl-butanoic acid

Kyselina isovalerova

Isobutyl formic acid

Isovaleriansaeure

FEMA No. 3102

3-methyl-n-butyric acid

Isovaleric acid (natural)

FEMA Number: 3102

3-Methylbuttersaeure

3-methyl butyric acid

3-methyl-butyric acid

NSC 62783

HSDB 629

.beta.-Methylbutyric acid

EINECS 207-975-3

MFCD00002726

b-Methylbutyric acid

UNII-1BR7X184L5

BRN 1098522

DELPHINIC-ACID

DTXSID5029182

CHEBI:28484

AI3-24132

1BR7X184L5

NSC-62783

3,4-Diisovaleryl adrenaline

DTXCID309182

3-Methyl-d3-butyric--d4 Acid

EC 207-975-3

4-02-00-00895 (Beilstein Handbook Reference)

Butanoic acid, 3-methyl-, (R)-

isopropylacetate

IVA

ISOVALERIC ACID (MART.)

ISOVALERIC ACID [MART.]

Kyselina isovalerova [Czech]

92634-50-9

methyl butanoic acid

METHYLBUTANOIC ACID

b-Methylbutyrate

iso-valeric acid

3-Methylbutanoicacid

iso-C4H9COOH

Isovaleric acid, 99%

bmse000373

SCHEMBL43436

ISOVALERIC ACID [MI]

ISOVALERIC ACID [FCC]

ISOVALERIC ACID [FHFI]

ISOVALERIC ACID [HSDB]

CHEMBL568737

WLN: QV1Y1&1

ISOVALERIC ACID [WHO-DD]

AMY40214

BCP32116

NSC62783

STR08356

Isovaleric acid, analytical standard

Tox21_201604

BBL027399

Isovaleric acid (mixture of isomers)

LMFA01020181

s6287

STL146358

AKOS000119861

Isovaleric acid, >=99%, FCC, FG

CS-W013696

DB03750

HY-W012980

MCULE-5805071360

3-Methylbutyric acid: isopropyl-Acetate

Isovaleric acid sodium salt (Salt/Mix)

Isovaleric acid, natural, >=98%, FG

NCGC00249082-01

NCGC00259153-01

35915-22-1

CAS-503-74-2

3-Methylbutyric acid: isopropyl-Acetic acid

M0182

NS00001831

EN300-19718

C08262

D78213

Q415536

J-522594

F2191-0067

Z104474910

3-Methylbutanoic acid;3-Methylbutyric acid;Isopentanoic acid

InChI=1/C5H10O2/c1-4(2)3-5(6)7/h4H,3H2,1-2H3,(H,6,7

The Henry's Law constant for isovaleric acid was measured as 8.33X10-7 atm-cu m/mole(1). This value indicates that isovaleric acid will volatilize slowly from water surfaces(2,SRC). Based on this Henry's Law constant, the estimated volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec) is estimated as approximately 45 days(2,SRC). The estimated volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is estimated as approximately 330 days(2,SRC). In addition, a pKa of 4.78 for isovaleric acid(3) indicates that isovaleric acid will not significantly volatilize from water as it will exist predominately in the ionic form under environmental pHs(SRC). Isovaleric acid's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). Isovaleric acid is not expected to volatilize from dry soil surfaces(SRC) based on a measured vapor pressure of 0.44 mm Hg(4).
Literature: (1) Khan I, Brimblecombe P; J Aerosol Sci 23: S897-S900 (1992) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington,DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Leung HW, Paustenbach DJ; Am J Ind Med 18: 714-23 (1990) (4) Yaws CL; Handbook of Vapor Pressure, Vol 2 C5 to C7 Compounds, Houston,TX: Gulf Publ Co. p. 387 (1994)

The Koc of isovaleric acid is estimated as approximately 100(SRC), using a measured log Kow of 1.16(1) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that isovaleric acid 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: 23 (1983)

3,4-DIHYDROXYBENZOIC ACID

protocatechuic acid

99-50-3

Protocatehuic acid

4-Carboxy-1,2-dihydroxybenzene

protocatechuate

4,5-Dihydroxybenzoic acid

Benzoic acid, 3,4-dihydroxy-

3,4-dihydroxybenzoate

CCRIS 6291

protocatechuicacid

EINECS 202-760-0

UNII-36R5QJ8L4B

MFCD00002509

NSC 16631

BRN 1448841

36R5QJ8L4B

DTXSID4021212

CHEBI:36062

PROTOCATECHOIC ACID

NSC-16631

Catechol-4-carboxylic Acid

3, 4-Dihydroxybenzoic acid

CHEMBL37537

MLS000737807

DTXCID601212

FEMA NO. 4430

PROTOCATECHUIC ACID (PCA)

DIHYDROXYBENZOIC ACID, 3,4-

1ykp

DROXIDOPA METABOLITE (PROTOCATECHOIC ACID)

3,4-Dihydroxy Benzoic Acid

NSC16631

DB03946

SMR000528167

C00230

D-3487

Hypogallic acid

b-Resorcylate

beta-Resorcylate

ProtocatechicAcid

b-resorcylic acid

4fht

Protacatechuic Acid

ZINCSELENITE

Carbohydroquinonic acid

cid_72

Protocatechuic Acid,(S)

Protocatechuic acid (M1)

bmse000328

3,4-dihydroxy-benzoic acid

3,4-dihydroxybenzoic acid (protocatechuic acid)

SCHEMBL39435

3,4-Dihydroxybenzoate, VIII

Pyrocatechol-4-carboxylic Acid

PROTOCATECHUIC ACID [MI]

HMS2270A17

KUC104409N

HY-N0294

Tox21_200167

BBL012232

BDBM50100861

s3975

STL163570

AKOS000119632

AC-9617

CCG-207950

CS-6092

KSC-10-128

MCULE-8964889860

CAS-99-50-3

NCGC00246757-01

NCGC00246757-02

NCGC00257721-01

3,4-DIHYDROXYBENZOIC ACID [INCI]

AS-10808

SY014104

DB-021903

AM20060767

NS00014667

3,4-Dihydroxybenzoic acid, >=97.0% (T)

EN300-21544

3,4-Dihydroxybenzoic acid, analytical standard

F11285

3,4-dihydroxybenzoate;3,4-Dihydroxybenzoic acid

A846038

AE-562/40524392

Q418599

976C8CCE-B25D-4E0A-9A6F-3CEEA7A6964F

Z104501142

3,4-Dihydroxybenzoic acid, Vetec(TM) reagent grade, 97%

PROTOCATECHOIC ACID (CONSTITUENT OF MARITIME PINE)

Protocatechuic acid, primary pharmaceutical reference standard

PROTOCATECHOIC ACID (CONSTITUENT OF MARITIME PINE) [DSC]

Protocatechuic acid, United States Pharmacopeia (USP) Reference Standard

InChI=1/C7H6O4/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,8-9H,(H,10,11

1225528-47-1

4-HYDROXYBENZOIC ACID

99-96-7

p-Hydroxybenzoic acid

4-Carboxyphenol

p-Salicylic acid

Benzoic acid, 4-hydroxy-

para-Hydroxybenzoic acid

Benzoic acid, p-hydroxy-

p-carboxyphenol

Paraben-acid

4-Hydroxybenzoesaeure

p-Oxybenzoesaure

Kyselina 4-hydroxybenzoova

p-Oxybenzoesaure [German]

4-Hydroxybenzoicacid

NSC 4961

PHBA

parahydroxybenzoic acid

Acido p-idrossibenzoico

4-hydroxy-benzoic acid

Hydroxybenzoic acid

HSDB 7233

Acido p-idrossibenzoico [Italian]

Kyselina 4-hydroxybenzoova [Czech]

EINECS 202-804-9

UNII-JG8Z55Y12H

CCRIS 8812

JG8Z55Y12H

DTXSID3026647

CHEBI:30763

HYDROXYBENZOIC ACID, PARA

p-hydroxy benzoic acid

AI3-01003

p-hydroxy-Benzoic acid

NSC-4961

Benzoic acid, 4-hydroxy

Hydroxybenzenecarboxylic acid

4-HBA

CHEMBL441343

DTXCID806647

FEMA NO. 3986

EC 202-804-9

MFCD00002547

3pcc

3pch

4-hydroxy-benzoate

4-hydroxy benzoic acid

Benzoic acid, p-hydroxy

WLN: QVR DQ

PHB

CAS-99-96-7

NSC4961

SALICYLIC ACID IMPURITY A (EP IMPURITY)

SALICYLIC ACID IMPURITY A [EP IMPURITY]

DB04242

NCGC00166040-01

ACETYLSALICYLIC ACID IMPURITY A (EP IMPURITY)

ACETYLSALICYLIC ACID IMPURITY A [EP IMPURITY]

PROPYL HYDROXYBENZOATE IMPURITY A (EP IMPURITY)

PROPYL HYDROXYBENZOATE IMPURITY A [EP IMPURITY]

METHYL PARAHYDROXYBENZOATE IMPURITY A (EP IMPURITY)

METHYL PARAHYDROXYBENZOATE IMPURITY A [EP IMPURITY]

C00156

p-Salicylate

AE-848/32195059

p-hydroxy-Benzoate

4-hydoxybenzoic acid

4-hyroxybenzoic acid

phenol derivative, 8

4-hydroxylbenzoic acid

4-Hydroxy-benzoesaeure

4-hydroxybenzoi c acid

PHLORETIN_met004

4-hydroxyl benzoic acid

4-Hydroxybenzoate, III

AVOBENZONE_met002

para-hydroxy benzoic acid

bmse000092

bmse000583

SCHEMBL4110

BIDD:ER0706

4-Hydroxybenzenecarboxylic acid

p-Hydroxybenzoic Acid, Reagent

BDBM26194

P-HYDROXYBENZOIC ACID [MI]

CS-D1180

HY-Y0264

STR01287

Tox21_202342

Tox21_303301

AC-008

BBL011981

s3754

STL138745

4-HYDROXYBENZOIC ACID [FHFI]

4-HYDROXYBENZOIC ACID [HSDB]

4-HYDROXYBENZOIC ACID [INCI]

4-Hydroxybenzoic acid, >=99%, FG

AKOS000119033

AM87513

CCG-266143

MCULE-1367764897

NCGC00166040-02

NCGC00257058-01

NCGC00259891-01

H0207

NS00005418

4-Hydroxybenzoic acid, ReagentPlus(R), 99%

EN300-21461

D86505

4-Hydroxybenzoic acid, ReagentPlus(R), >=99%

4-Hydroxybenzoic acid, puriss., >=99.0% (T)

A858402

Q229970

46DD083D-BFD3-4CE1-B2D9-6C6D5FEFD3D9

J-660066

W-100004

4-Hydroxybenzoic acid, Vetec(TM) reagent grade, 99%

2-3-4'-TRIHYDROXY-4-METHOXYBENZOPHENONE_met005

F2191-0237

Z104498098

2-3-DIHYDROXY-4-METHOXY-4'-ETHOXYBENZOPHENONE_met009

4-Hydroxybenzoic acid, certified reference material, TraceCERT(R)

4-Hydroxybenzoic acid, Pharmaceutical Secondary Standard; Certified Reference Material

InChI=1/C7H6O3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H,(H,9,10

30729-36-3

The Henry's Law constant for 4-hydroxybenzoic acid is estimated as 7.2X10-12 atm-cu m/mole(SRC) derived from its extrapolated vapor pressure, 1.9X10-7 mm Hg(1), and water solubility, 5000 mg/L(2). This Henry's Law constant indicates that 4-hydroxybenzoic acid is expected to be essentially nonvolatile from water surfaces(3). 4-Hydroxybenzoic acid's estimated Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to occur(SRC). In addition, 4-hydroxybenzoic acid's pKa value of 4.54(4) indicates that it will exist almost entirely as an anion at pH values of 5 to 9 and therefore volatilization from water and moist soil surfaces is not expected to be an important fate process(SRC). 4-Hydroxybenzoic acid is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Jones AH; J Chem Eng Data 5:196-200 (1960) (2) Yalkowsky SH, He Y, eds; Handbook of aqueous solubility data. Boca Raton, FL: CRC Press p. 377 (2003) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) Bykova LN et al; Zh Obshch Khim 40: 2295-300 (1970)

Koc values of 142, 20, and 14 were measured according to a modified version of OECD guideline 106 for 4-hydroxybenzoic acid in a podzol (pH=2.8, C organic=4.85%, sand:silt:clay=89.2:8.2:2.6%), alfisol (pH=6.7, C organic=1.25%, sand:silt:clay=69.7:14.4:15.9%), and a sediment (pH=7.1, C organic=1.58%, sand:silt:clay=5.5:58.8:35.7%), respectively(1). According to a classification scheme(2), these Koc values suggest that 4-hydroxybenzoic acid is expected to have high to very high mobility in soil. The pKa of 4-hydroxybenzoic acid is 4.54(3), indicating that this compound will primarily exist in anion form in the environment and anions generally do not adsorb more strongly to organic carbon and clay than their neutral counterparts(4).
Literature: (1) Vonoepen B et al; Chemosphere 22: 285-304 (1991) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Bykova LN et al; Zh Obshch Khim 40: 2295-300 (1970) (4) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)