4-[1-Hydroxy-2-(isopropylamino)ethyl]-1,2-benzenediol
Oc1ccc(cc1O)C(O)CNC(C)C CopyCopied
InChI=1S/C11H17NO3/c1-7(2)12-6-11(15)8-3-4-9(13)10(14)5-8/h3-5,7,11-15H,6H2,1-2H3 CopyCopied
JWZZKOKVBUJMES-UHFFFAOYSA-N CopyCopied
Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts
Isoprenaline [Wiki]
1,2-Benzenediol, 4-(1-hydroxy-2-((1-methylethyl)amino)ethyl)-
1,2-benzenediol, 4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-
231-687-7 [EINECS]
3,4-Dihydroxy-a-[(isopropylamino)methyl]benzyl Alcohol
3,4-Dihydroxy-α-(isopropylaminomethyl)-benzyl alcohol
3,4-Dihydroxy-α-[(isopropylamino)methyl]benzyl alcohol
4-(1-Hydroxy-2-(isopropylamino)ethyl)benzene-1,2-diol
4-[1-Hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol
4-[1-hydroxy-2-(propan-2-ylamino)ethyl]benzene-1,2-diol
4-[1-Hydroxy-2-[(1-methylethyl)amino]ethyl]-1,2-benzenediol
4-{1-hydroxy-2-[(1-methylethyl)amino]ethyl}benzene-1,2-diol
4-{1-hydroxy-2-[(1-méthyléthyl)amino]éthyl}benzène-1,2-diol
4-{1-Hydroxy-2-[(1-methylethyl)amino]ethyl}benzol-1,2-diol
6700-39-6 [RN]
a-(Isopropylaminomethyl)protocatechuyl Alcohol
AEROLONE
Aerolone Solution
Aerotrol
Aleudrin
Benzyl alcohol, 3,4-dihydroxy-α-((isopropylamino)methyl)-, (-)-
Isomenyl
isoproterenol [Wiki]
Isupren
N-Isopropyl-b-dihydroxyphenyl-b-hydroxyethylamine
Aleudrine
IpA
Isuprel Mistometer
MEDIHALER-ISO
NORISODRINE AEROTROL
VAPO-ISO
7683-59-2
(.+ -.)-Isopropylnoradrenaline hydrochloride
(+ -)-Isopropylnoradrenaline hydrochloride
(±)-Isoprenaline
(±)-Isoprenaline hydrochloride
(±)-Isoproterenol hydrochloride
1-(3,4-Dihydroxyphenyl)-2-(isopropylamino)ethanol
1-(3,4-Dihydroxyphenyl)-2-isopropylaminoethanol
1,2-Benzenediol, 4-(1-hydroxy-2-((1-methylethyl)amino)ethyl)- (9CI)
1,2-Benzenediol, 4-(1-hydroxy-2-((1-methylethyl)amino)ethyl)-, (±)-
1,2-Benzenediol, 4-[1-hydroxy-2-[ (1-methylethyl)amino]ethyl]-
1,2-Benzenediol, 4-[1-hydroxy-2-[ (1-methylethyl)amino]ethyl]-, hydrochloride
1,2-Benzenediol, 4-[1-hydroxy-2-[ (1-methylethyl)amino]ethyl]-, hydrochloride, (.+ -.)-
1,2-Benzenediol, 4-[1-hydroxy-2-[(1-methylethyl)
149-53-1 [RN]
200-089-8 [EINECS]
2213857 [Beilstein]
2964-04-7 [RN]
3,4-Dihydroxy-α-((isopropylamino)methyl)benzyl alcohol
3-13-00-02387 (Beilstein Handbook Reference) [Beilstein]
337376-15-5
4-(1-Hydroxy-2-((1-methylethyl)amino)ethyl)-1,2-benzenediol
4-(1-Hydroxy-2(isopropylamino)ethyl)-benzene 1,2-diol
4-(1-hydroxy-2-(isopropylamino)ethyl)benzene-1,2-diol hydrochloride
4-(1-Hydroxy-2-isopropylamino-ethyl)-benzene-1,2-diol hydrochloride
4-{1-hydroxy-2-[(methylethyl)amino]ethyl}benzene-1,2-diol
46388-38-9 [RN]
51-30-9 [RN]
51-30-9(HCL)
7683-59-2 [RN]
949-36-0 [RN]
Aludrin
Aludrine
Asiprenol
Asmalar
Assiprenol
Bellasthman
Benzyl alcohol, 3, 4-dihydroxy-α-[ (isopropylamino)methyl]-
Benzyl alcohol, 3, 4-dihydroxy-α-[ (isopropylamino)methyl]-, hydrochloride
Benzyl alcohol, 3, 4-dihydroxy-α-[ (isopropylamino)methyl]-, hydrochloride, (.+ -.)-
Benzyl alcohol, 3, 4-dihydroxy-α-[ (isopropylamino)methyl]-, hydrochloride, (+ -)-
Benzyl alcohol, 3,4-dihydroxy-α-((isopropylamino)methyl)-
Benzyl alcohol, 3,4-dihydroxy-α-((isopropylamino)methyl)-, (+)-
Benzyl alcohol, 3,4-dihydroxy-α-((isopropylamino)methyl)-, (±)-
component of Aerolone Compound
component of Naxid
Dihydroxyphenylethanolisopropylamine
dl-Ipr
dl-Isadrine
dl-Isadrine hydrochloride
DL-Isoprenaline hydrochloride
dl-Isopropylnoradrenaline
DL-Isopropylnoradrenaline hydrochloride
DL-Isopropylnorepinephrine
dl-Isopropylnorepinephrine hydrochloride
DL-Isoproterenol hydrochloride
dl-N-Isopropylnoradrenaline
Epinephrine isopropyl homolog
Euspiran
Iprenol
Isadrine
Isadrine-hydrochloride
Isonorene
Isonorin
Isoprenalin
isoprenalina [Spanish]
Isoprenaline hydrochloride
isoprenalinum [Latin]
ISOPROP
Isopropydrin
Isopropyl noradrenaline
Isopropyladrenaline
Isopropylaminomethyl(3, 4-dihydroxyphenyl)carbinol
Isopropylarterenol
Isopropylnoradrenaline
Isopropylnorepinephrine
Isopropylnorepinephrine-hydrochloride
Isoproterenol hydrochloride
Isoproterenolum
Isorenin
Isuprel [Wiki]
Izadrin
Lomupren
Neodrenal
Neo-epinine
N-Isopropyl-DL-noradrenaline hydrochloride
N-Isopropylnoradrenaline
N-Isopropylnorepinephrine
N-Isopropyl-β-dihydroxyphenyl-β-hydroxyethylamine
NORISODRINE
Novodrin
Proternol
Protocatechuyl alcohol, α-(isopropylaminomethyl)-
Protocatechuyl alcohol, α-(isopropylamino-methyl),-
Racemic isoprenaline
Racemic isoproterenol
Respifral
Saventrine
Sooner [Wiki]
Vapo-N-Iso
α-(Isopropylaminomethyl)protocatechuyl alcohol
α-(Isopropylaminomoethyl)protocatechuyl alcohol
AIDS026864 [DBID]
AIDS-026864 [DBID]
BRN 2213857 [DBID]
C07056 [DBID]
CCRIS 3081 [DBID]
CHEBI:6046 [DBID]
DivK1c_000894 [DBID]
ICI 46399 [DBID]
KBio1_000894 [DBID]
KBio2_001429 [DBID]
KBio2_003997 [DBID]
KBio2_006565 [DBID]
KBio3_001428 [DBID]
KBioGR_000427 [DBID]
KBioSS_001429 [DBID]
nchembio801-comp2 [DBID]
NCI-C55630 [DBID]
NINDS_000894 [DBID]
NSC 33791 [DBID]
NSC 9975 [DBID]
NSC33791 [DBID]
NSC37745 [DBID]
NSC89747 [DBID]
NSC9975 [DBID]
Prestwick0_001097 [DBID]
Prestwick1_001097 [DBID]
SPBio_001042 [DBID]
SPBio_003057 [DBID]
Spectrum_000949 [DBID]
Spectrum2_001061 [DBID]
Spectrum3_000474 [DBID]
Spectrum4_000024 [DBID]
WIN 5162 [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) = 0.21 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42): Boiling Pt (deg C): 361.59 (Adapted Stein & Brown method) Melting Pt (deg C): 132.76 (Mean or Weighted MP) VP(mm Hg,25 deg C): 7.6E-008 (Modified Grain method) MP (exp database): 170.5 deg C Subcooled liquid VP: 2.42E-006 mm Hg (25 deg C, Mod-Grain method) Water Solubility Estimate from Log Kow (WSKOW v1.41): Water Solubility at 25 deg C (mg/L): 9.735e+005 log Kow used: 0.21 (estimated) no-melting pt equation used Water Sol Estimate from Fragments: Wat Sol (v1.01 est) = 1e+006 mg/L ECOSAR Class Program (ECOSAR v0.99h): Class(es) found: Aliphatic Amines Phenols Benzyl Alcohols Henrys Law Constant (25 deg C) [HENRYWIN v3.10]: Bond Method : 1.24E-018 atm-m3/mole Group Method: Incomplete Henrys LC [VP/WSol estimate using EPI values]: 2.170E-014 atm-m3/mole Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]: Log Kow used: 0.21 (KowWin est) Log Kaw used: -16.295 (HenryWin est) Log Koa (KOAWIN v1.10 estimate): 16.505 Log Koa (experimental database): None Probability of Rapid Biodegradation (BIOWIN v4.10): Biowin1 (Linear Model) : 1.1911 Biowin2 (Non-Linear Model) : 0.9829 Expert Survey Biodegradation Results: Biowin3 (Ultimate Survey Model): 3.0295 (weeks ) Biowin4 (Primary Survey Model) : 3.7950 (days ) MITI Biodegradation Probability: Biowin5 (MITI Linear Model) : 0.4210 Biowin6 (MITI Non-Linear Model): 0.2921 Anaerobic Biodegradation Probability: Biowin7 (Anaerobic Linear Model): 0.7554 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): 0.000323 Pa (2.42E-006 mm Hg) Log Koa (Koawin est ): 16.505 Kp (particle/gas partition coef. (m3/ug)): Mackay model : 0.0093 Octanol/air (Koa) model: 7.85E+003 Fraction sorbed to airborne particulates (phi): Junge-Pankow model : 0.251 Mackay model : 0.427 Octanol/air (Koa) model: 1 Atmospheric Oxidation (25 deg C) [AopWin v1.92]: Hydroxyl Radicals Reaction: OVERALL OH Rate Constant = 155.2650 E-12 cm3/molecule-sec Half-Life = 0.069 Days (12-hr day; 1.5E6 OH/cm3) Half-Life = 0.827 Hrs Ozone Reaction: No Ozone Reaction Estimation Reaction With Nitrate Radicals May Be Important! Fraction sorbed to airborne particulates (phi): 0.339 (Junge,Mackay) Note: the sorbed fraction may be resistant to atmospheric oxidation Soil Adsorption Coefficient (PCKOCWIN v1.66): Koc : 379.6 Log Koc: 2.579 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 = 0.500 (BCF = 3.162) log Kow used: 0.21 (estimated) Volatilization from Water: Henry LC: 1.24E-018 atm-m3/mole (estimated by Bond SAR Method) Half-Life from Model River: 6.863E+014 hours (2.859E+013 days) Half-Life from Model Lake : 7.487E+015 hours (3.119E+014 days) Removal In Wastewater Treatment: Total removal: 1.85 percent Total biodegradation: 0.09 percent Total sludge adsorption: 1.76 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 5.84e-011 1.65 1000 Water 38.2 360 1000 Soil 61.8 720 1000 Sediment 0.0709 3.24e+003 0 Persistence Time: 585 hr
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