1,2-Dihydroxy-9,10-anthraquinone
O=C2c1ccccc1C(=O)c3c2ccc(O)c3O CopyCopied
InChI=1S/C14H8O4/c15-10-6-5-9-11(14(10)18)13(17)8-4-2-1-3-7(8)12(9)16/h1-6,15,18H CopyCopied
RGCKGOZRHPZPFP-UHFFFAOYSA-N CopyCopied
Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts
1,2-Dihydroxy-9,10-anthrachinon [German]
1,2-Dihydroxy-9,10-anthraquinone [ACD/IUPAC Name]
1,2-Dihydroxyanthracen-9,10-dion [German]
72-48-0 [RN]
9,10-anthracenedione, 1,2-dihydroxy-
Acid Metachrome Red B
Acid Mordant Red B
Alizarin [Wiki]
C Ext. Red 62
D & C Orange No. 15
1, 2-Anthraquinonediol
1,2-Anthraquinonediol
1,2-Dihydroxy anthraquinone
1,2-Dihydroxy-9,10-anthracenedione
1,2-dihydroxyanthra-9,10-quinone
1,2-dihydroxyanthracene-9,10-dione
1,2-Dihydroxyanthrachinon
1,2-dihydroxyanthraquinone
1,2-Dihydroxy-anthraquinone
117-10-2 [RN]
130-22-3 [RN]
1309-37-1 [RN]
1322-60-7 [RN]
1332-37-2 [RN]
1914037 [Beilstein]
200-782-5 [EINECS]
204-173-5 [EINECS]
204-981-8 [EINECS]
215-168-2 [EINECS]
215-570-8 [EINECS]
4-08-00-03256 (Beilstein Handbook Reference) [Beilstein]
65271-80-9 [RN]
9, 10-Anthracenedione, 1,2-dihydroxy-
9,10-Anthracenedione
Alizarin B
ALIZARIN RED
Alizarina
ALIZARINE [Wiki]
Alizarine 3B
Alizarine B
Alizarine Lake Red 2P
Alizarine Lake Red 3P
Alizarine Lake Red IPX
Alizarine NAC
Alizarine Red
Alizarine Red B
Alizarine Red B2
Alizarine Red IP
Alizarine Red IPP
Alizarine Red L
Alizarinprimeveroside
Alizerine NAC
Alizerine Red IPP
Anthraquinone, 1,2-dihydroxy-
ATHRAQUINONES A
Az
C.I. Mordant Red 11
C.I. Mordant Red 11C
C.I. Pigment Red 83
C.I. Pigment Red 83C
C010078
Certiqual Alizarine
Certiqual Alizarine D
D and C Orange No. 15
D And C Orange Number 15
D and C Orange Number 15D
Deep Crimson Madder 10821
Deep Crimson Madder 10821E
Dihydroxy-9,10-anthracenedione
DIHYDROXYANTHRAQUINONE
Eljon madder
Eljon Madder M
Hystazarin
LN: L C666 BV IVJ EQ FQ1
Mitsui Alizarine B
Mitsui Alizarine BS
MORDANT RED 11
Pigment Red 83
Sanyo Carmine L2B
Sanyo Carmine l2BT
TL8005063
TURKEY RED
Turkey Red (VAN)
Turkey Red W
茜素 [Chinese]
05560_FLUKA [DBID]
122777_SIAL [DBID]
32612_RIEDEL [DBID]
333174_SIAL [DBID]
AI3-18244 [DBID]
AIDS001373 [DBID]
AIDS-001373 [DBID]
BRN 1914037 [DBID]
C.I. 58000 [DBID]
C.I. 58000C [DBID]
C01474 [DBID]
CBDivE_014227 [DBID]
CCRIS 3530 [DBID]
CHEBI:16866 [DBID]
CI 58000 [DBID]
DivK1c_006416 [DBID]
KBio1_001360 [DBID]
KBio2_000866 [DBID]
KBio2_003434 [DBID]
KBio2_006002 [DBID]
KBio3_001204 [DBID]
KBioGR_002050 [DBID]
KBioSS_000866 [DBID]
NCI60_041501 [DBID]
NSC 7212 [DBID]
NSC7212 [DBID]
SDCCGMLS-0066502.P001 [DBID]
SPBio_000613 [DBID]
SpecPlus_000320 [DBID]
Spectrum_000386 [DBID]
Spectrum2_000397 [DBID]
Spectrum3_000262 [DBID]
Spectrum4_001555 [DBID]
ZINC03860973 [DBID]
Data supplied by datasources and users.
Predicted data is generated using the ACD/Labs’ ACD/PhysChem Suite, for more information see their website.
Predicted data is generated using the US Environmental Protection Agency’s EPISuite™, for more information see their website.
Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 estimate) = 3.16 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42): Boiling Pt (deg C): 433.26 (Adapted Stein & Brown method) Melting Pt (deg C): 181.42 (Mean or Weighted MP) VP(mm Hg,25 deg C): 7.15E-011 (Modified Grain method) MP (exp database): 289.5 deg C BP (exp database): 430 deg C VP (exp database): 8.76E-10 mm Hg at 25 deg C Subcooled liquid VP: 3.62E-007 mm Hg (25 deg C, exp database VP ) Water Solubility Estimate from Log Kow (WSKOW v1.41): Water Solubility at 25 deg C (mg/L): 15.79 log Kow used: 3.16 (estimated) no-melting pt equation used Water Sol (Exper. database match) = 400 mg/L ( deg C) Exper. Ref: YALKOWSKY,SH & DANNENFELSER,RM (1992) Water Sol Estimate from Fragments: Wat Sol (v1.01 est) = 255.83 mg/L Wat Sol (Exper. database match) = 400.00 Exper. Ref: YALKOWSKY,SH & DANNENFELSER,RM (1992) ECOSAR Class Program (ECOSAR v0.99h): Class(es) found: Phenols Henrys Law Constant (25 deg C) [HENRYWIN v3.10]: Bond Method : 4.33E-014 atm-m3/mole Group Method: Incomplete Henrys LC [VP/WSol estimate using EPI values]: 1.431E-012 atm-m3/mole Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]: Log Kow used: 3.16 (KowWin est) Log Kaw used: -11.752 (HenryWin est) Log Koa (KOAWIN v1.10 estimate): 14.912 Log Koa (experimental database): None Probability of Rapid Biodegradation (BIOWIN v4.10): Biowin1 (Linear Model) : 0.8785 Biowin2 (Non-Linear Model) : 0.6245 Expert Survey Biodegradation Results: Biowin3 (Ultimate Survey Model): 2.7361 (weeks-months) Biowin4 (Primary Survey Model) : 3.5361 (days-weeks ) MITI Biodegradation Probability: Biowin5 (MITI Linear Model) : 0.4107 Biowin6 (MITI Non-Linear Model): 0.2603 Anaerobic Biodegradation Probability: Biowin7 (Anaerobic Linear Model): -0.3588 Ready Biodegradability Prediction: NO Hydrocarbon Biodegradation (BioHCwin v1.01): Structure incompatible with current estimation method! Sorption to aerosols (25 Dec C)[AEROWIN v1.00]: Vapor pressure (liquid/subcooled): 4.83E-005 Pa (3.62E-007 mm Hg) Log Koa (Koawin est ): 14.912 Kp (particle/gas partition coef. (m3/ug)): Mackay model : 0.0622 Octanol/air (Koa) model: 200 Fraction sorbed to airborne particulates (phi): Junge-Pankow model : 0.692 Mackay model : 0.833 Octanol/air (Koa) model: 1 Atmospheric Oxidation (25 deg C) [AopWin v1.92]: Hydroxyl Radicals Reaction: OVERALL OH Rate Constant = 9.8450 E-12 cm3/molecule-sec Half-Life = 1.086 Days (12-hr day; 1.5E6 OH/cm3) Half-Life = 13.037 Hrs Ozone Reaction: No Ozone Reaction Estimation Reaction With Nitrate Radicals May Be Important! Fraction sorbed to airborne particulates (phi): 0.762 (Junge,Mackay) Note: the sorbed fraction may be resistant to atmospheric oxidation Soil Adsorption Coefficient (PCKOCWIN v1.66): Koc : 507.7 Log Koc: 2.706 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]: Rate constants can NOT be estimated for this structure! Bioaccumulation Estimates from Log Kow (BCFWIN v2.17): Log BCF from regression-based method = 0.894 (BCF = 7.834) log Kow used: 3.16 (estimated) Volatilization from Water: Henry LC: 4.33E-014 atm-m3/mole (estimated by Bond SAR Method) Half-Life from Model River: 2.096E+010 hours (8.732E+008 days) Half-Life from Model Lake : 2.286E+011 hours (9.526E+009 days) Removal In Wastewater Treatment: Total removal: 7.30 percent Total biodegradation: 0.14 percent Total sludge adsorption: 7.17 percent Total to Air: 0.00 percent (using 10000 hr Bio P,A,S) Level III Fugacity Model: Mass Amount Half-Life Emissions (percent) (hr) (kg/hr) Air 0.000117 26.1 1000 Water 12.3 900 1000 Soil 87.3 1.8e+003 1000 Sediment 0.403 8.1e+003 0 Persistence Time: 1.8e+003 hr
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