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[ CAS No. 16415-12-6 ] {[proInfo.proName]}

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Chemical Structure| 16415-12-6
Chemical Structure| 16415-12-6
Structure of 16415-12-6 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Kueyoung E. Kim ; Wangyang Xue ; Lauren D. Zarzar DOI:

Abstract: Hypothesis Sessile droplets solubilizing in surfactant solution are frequently encountered in practice, but the factors governing their non-equilibrium dynamics are not well understood. Here, we investigate mechanisms by which solubilizing, sessile oil droplets in aqueous surfactant solution dewet from hydrophobic substrates and spread on hydrophilic substrates. Experiments We quantify the dependence of droplet contact line dynamics on drop size and oil, surfactant, and substrate chemistries. We consider halogenated oils as well as aromatic oils and focus on common nonionic nonylphenol ethoxylate . We correlate these results with measurements of the interfacial tensions. Findings Counter-intuitively, under a range of conditions, we observe complete dewetting of oil from hydrophobic substrates but spreading on hydrophilic substrates. The timescales needed to reach a steady-state contact angle vary widely, with some droplets examined taking over a day. We find that surfactant surface adsorption governs the contact angle on shorter timescales, while partitioning of surfactant from water to oil, and oil solubilization into the water, act on longer timescales to facilitate the complete dewetting. Understanding of the role played by surfactant and oil transport presents opportunities for tailoring sessile droplet behaviors and controlling droplet dynamics under conditions that would previously not have been considered.

Keywords: Wetting ; Surfactant ; Adsorption ; Partitioning ; Sessile Droplet

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Product Details of [ 16415-12-6 ]

CAS No. :16415-12-6 MDL No. :MFCD00069149
Formula : C19H42O3Si Boiling Point : -
Linear Structure Formula :- InChI Key :RSKGMYDENCAJEN-UHFFFAOYSA-N
M.W : 346.62 Pubchem ID :85406
Synonyms :

Calculated chemistry of [ 16415-12-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 23
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 18
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 104.57
TPSA : 27.69 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -2.32 cm/s

Lipophilicity

Log Po/w (iLOGP) : 5.71
Log Po/w (XLOGP3) : 8.59
Log Po/w (WLOGP) : 6.35
Log Po/w (MLOGP) : 3.36
Log Po/w (SILICOS-IT) : 4.88
Consensus Log Po/w : 5.78

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -6.21
Solubility : 0.000212 mg/ml ; 0.000000613 mol/l
Class : Poorly soluble
Log S (Ali) : -9.05
Solubility : 0.000000311 mg/ml ; 0.0000000009 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -6.79
Solubility : 0.0000563 mg/ml ; 0.000000163 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 5.17

Safety of [ 16415-12-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 16415-12-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 16415-12-6 ]

[ 16415-12-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 5894-60-0 ]
  • [ 16415-12-6 ]
Reference: [1] Patent: US6150551, 2000, A,
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