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Search term: UITSPQLTFPTHJZ-XTLGRWLVBY
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Inherent Properties, Identifiers and References
ChemSpider ID: 56052
Empirical Formula: C15H30O10
Molecular Weight: 370.3927
Nominal Mass: 370 Da
Average Mass: 370.3927 Da
Monoisotopic Mass: 370.183897 Da
Systematic Name: 2-[(2R,6R)-3,5-bis(2-hydroxyethoxy)-2-(2-hydroxyethoxymethyl)-6-m​ethoxy-tetrahydropyran-4-yl]oxyethanol
SMILES: O(C1C(OCCO)C(OCCO)[C@H](O[C@H]1OC)COCCO)CCO
InChI: InChI=1/C15H30O10/c1-20-15-14(24-9-5-19)13(23-8-4-18)12(22-7-3-17​)11(25-15)10-21-6-2-16/h11-19H,2-10H2,1H3/t11-,12?,13?,14?,15-/m1​/s1
InChIKey: UITSPQLTFPTHJZ-XTLGRWLVBY
Std. InChI: InChI=1S/C15H30O10/c1-20-15-14(24-9-5-19)13(23-8-4-18)12(22-7-3-1​7)11(25-15)10-21-6-2-16/h11-19H,2-10H2,1H3/t11-,12?,13?,14?,15-/m​1/s1
Std. InChIKey: UITSPQLTFPTHJZ-XTLGRWLVSA-N
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Names and Synonyms

Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts

195378-75​-7 [RN]

68239-42-9 [RN]

Ethoxylat​ed methyl​ beta-D-g​lucoside

Poly(oxy-​1,2-ethan​ediyl), a​lpha-hydr​o-omega-h​ydroxy-, ​ether wit​h methyl ​beta-D-gl​ucopyrano​side (4:1)

Poly(oxy-​1,2-ethan​ediyl), a​lpha-hydr​o-omega-h​ydroxy-, ​ether wit​h methylb​eta-D-glu​copyranos​ide (4:1)

Polyethyl​ene glyco​l beta-me​thyl gluc​oside eth​er (4:1)

ACD/LogP: -2.22 # of Rule of 5 Violations: 1
ACD/LogD (pH 5.5): -2.22 ACD/LogD (pH 7.4): -2.22
ACD/BCF (pH 5.5): 1 ACD/BCF (pH 7.4): 1
ACD/KOC (pH 5.5): 1.48 ACD/KOC (pH 7.4): 1.48
#H bond acceptors: 10 #H bond donors: 4
#Freely Rotating Bonds: 18 Polar Surface Area: 92.3 Å2
Index of Refraction: 1.511 Molar Refractivity: 85.93 cm3
Molar Volume: 286.7 cm3 Polarizability: 34.06 10-24cm3
Surface Tension: 55 dyne/cm Density: 1.29 g/cm3
Flash Point: 294 °C Enthalpy of Vaporization: 97.17 kJ/mol
Boiling Point: 562.6 °C at 760 mmHg Vapour Pressure: 5.34E-15 mmHg at 25°C
            
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  -4.26

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  516.94  (Adapted Stein & Brown method)
    Melting Pt (deg C):  220.51  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  4.34E-014  (Modified Grain method)
    Subcooled liquid VP: 5.33E-012 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):  1e+006
       log Kow used: -4.26 (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:
       Neutral Organics

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   9.09E-022  atm-m3/mole
   Group Method:   4.66E-035  atm-m3/mole
 Henrys LC [VP/WSol estimate using EPI values]:  2.115E-020 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  -4.26  (KowWin est)
  Log Kaw used:  -19.430  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  15.170
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :  -0.8780
   Biowin2 (Non-Linear Model)     :   0.0000
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   2.9685  (weeks       )
   Biowin4 (Primary Survey Model) :   3.7727  (days        )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :   0.7710
   Biowin6 (MITI Non-Linear Model):   0.1742
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model):  0.1752
 Ready Biodegradability Prediction:   YES

Hydrocarbon Biodegradation (BioHCwin v1.01):
    Structure incompatible with current estimation method!

 Sorption to aerosols (25 Dec C)[AEROWIN v1.00]:
  Vapor pressure (liquid/subcooled):  7.11E-010 Pa (5.33E-012 mm Hg)
  Log Koa (Koawin est  ): 15.170
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  4.22E+003 
       Octanol/air (Koa) model:  363 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  1 
       Mackay model           :  1 
       Octanol/air (Koa) model:  1 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant = 132.8602 E-12 cm3/molecule-sec
      Half-Life =     0.081 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =     0.966 Hrs
   Ozone Reaction:
      No Ozone Reaction Estimation
   Fraction sorbed to airborne particulates (phi): 1 (Junge,Mackay)
    Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
      Koc    :  10
      Log Koc:  1.000 

 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: -4.26 (estimated)

 Volatilization from Water:
    Henry LC:  9.09E-022 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River:  1.24E+018  hours   (5.165E+016 days)
    Half-Life from Model Lake : 1.352E+019  hours   (5.635E+017 days)

 Removal In Wastewater Treatment:
    Total removal:               1.85  percent
    Total biodegradation:        0.09  percent
    Total sludge adsorption:     1.75  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       5.18e-009       1.93         1000       
   Water     39              360          1000       
   Soil      60.9            720          1000       
   Sediment  0.0713          3.24e+003    0          
     Persistence Time: 579 hr




        
Descriptors: 0, 0, 0, 0, 0, 0, 0, 12, 0, 0, 4, 8, 0, 0, 26, 0, 0, 0, 0, 0, 0, 0, 0, 0
CategoryTargetPDB CodeLASSO Score
Other EnzymesGPB, glycogen phosphorylase1a8i0.87
Nuclear Hormone ReceptorsPPARg, peroxisome proliferator activated receptor1fm90.03
KinasesSRC, tyrosine kinase SRC2src0.01
Other EnzymesHMGR, hydroxymethylglutaryl-CoA reductase1hw80.01
Other EnzymesHIVPR, HIV protease1hpx0.01
KinasesHSP90, human heat shock protein 901uy60.01
MetalloenzymesPDE5, phosphodiesterase 51xp00.01
Nuclear Hormone ReceptorsMR, mineralocorticoid receptor2aa20.01
MetalloenzymesADA, adenosine deaminase1stw0.01
Other EnzymesPNP, purine nucleoside phosphorylase1b8o0.01
Other EnzymesPARP, poly(ADP-ribose) polymerase1efy0.01
Nuclear Hormone ReceptorsGR, glucocorticoid receptor1m2z0.00
Other EnzymesAmpC, AmpC beta-lactamase1xgj0.00
MetalloenzymesACE, angiotensin-converting enzyme1o860.00
Folate EnzymesGART, glycinamide ribonucleotide transformylase1c2t0.00
Nuclear Hormone ReceptorsER, estrogen receptor; agonist1l2i0.00
Nuclear Hormone ReceptorsPR, progesterone receptor1sr70.00
Folate EnzymesDHFR, dihydrofolate reductase3dfr0.00
Other EnzymesNA, neuraminidase1a4g0.00
KinasesVEGFr2, vascular endothelial growth factor receptor1vr20.00
KinasesFGFr1, fibroblast growth factor receptor kinase1agw0.00
KinasesTK, thymidine kinase1kim0.00
Other EnzymesInhA, enoyl ACP reductase1p440.00
Nuclear Hormone ReceptorsRXRa, retinoic X receptor R1mvc0.00
Other EnzymesAChE, acetylcholinesterase1eve0.00
Nuclear Hormone ReceptorsAR, androgen receptor1xq20.00
Nuclear Hormone ReceptorsER, estrogen receptor; antagonist3ert0.00
KinasesPDGFrb, platelet derived growth factor receptor kinaseN/A0.00
Serine ProteasesThrombin1ba80.00
Other EnzymesSAHH, S-adenosyl-homocysteine hydrolase1a7a0.00
Other EnzymesHIVRT, HIV reverse transcriptase1rt10.00
KinasesP38 MAP, P38 mitogen activated protein1kv20.00
KinasesEGFr, epidermal growth factor receptor1m170.00
Serine ProteasesFXa, factor Xa1f0r0.00
KinasesCDK2, cyclindependent kinase 21ckp0.00
MetalloenzymesCOMT, catechol O-methyltransferase1h1d0.00
Other EnzymesCOX-1, cyclooxygenase-11p4g0.00
Other EnzymesCOX-2, cyclooxygenase-21cx20.00
Other EnzymesALR2, aldose reductase1ah30.00
Serine ProteasesTrypsin1bju0.00