On the public citation graph

Greener Terpene–Terpene Eutectic Mixtures as Hydrophobic Solvents

https://doi.org/10.1021/acssuschemeng.9b04614
0 signed · 176 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9783527809479openalex-snapshot
Chemical Thermodynamics for Process Simulation
inferredcites →https://doi.org/10.1002/ardp.19352732509openalex-snapshot
Die heterogenen Gleichgewichte in Zweistoffsystemen mit Thymol als einer Komponente
inferredcites →https://doi.org/10.1002/cssc.200900186openalex-snapshot
Myrcene as a Natural Base Chemical in Sustainable Chemistry: A Critical Review
inferredcites →https://doi.org/10.1002/jps.2600790603openalex-snapshot
Sobrerol Enantiomers and Racemates: Solid-State Spectroscopy, Thermal Behavior, and Phase Diagrams
inferredcites →https://doi.org/10.1007/s00425-018-3056-xopenalex-snapshot
Terpenes and isoprenoids: a wealth of compounds for global use
inferredcites →https://doi.org/10.1016/0021-9614(70)90078-9openalex-snapshot
Molecular thermodynamics of fluid-phase equilibria
inferredcites →https://doi.org/10.1016/0304-3894(92)85068-copenalex-snapshot
Chemical substitution for 1,1,1-trichloroethane and methanol in an industrial cleaning operation
inferredcites →https://doi.org/10.1016/0378-3812(94)02600-6openalex-snapshot
Evaluation of activity coefficient models in prediction of alkane solid-liquid equilibria
inferredcites →https://doi.org/10.1016/j.algal.2016.05.005openalex-snapshot
One-pot bioconversion of algae biomass into terpenes for advanced biofuels and bioproducts
inferredcites →https://doi.org/10.1016/j.chroma.2018.07.070openalex-snapshot
Hydrophobic deep eutectic solvents as “green” extraction media for polycyclic aromatic hydrocarbons in aqueous samples
inferredcites →https://doi.org/10.1016/j.ejps.2004.08.008openalex-snapshot
Preparation of ibuprofen-loaded liquid suppository using eutectic mixture system with menthol
inferredcites →https://doi.org/10.1016/j.fluid.2017.04.020openalex-snapshot
Solvatochromic parameters of deep eutectic solvents formed by ammonium-based salts and carboxylic acids
inferredcites →https://doi.org/10.1016/j.jct.2013.12.012openalex-snapshot
Thermodynamic study of selected monoterpenes II
inferredcites →https://doi.org/10.1016/j.jct.2018.11.004openalex-snapshot
Polymorphism and thermophysical properties of l- and dl-menthol
inferredcites →https://doi.org/10.1016/j.molliq.2017.06.099openalex-snapshot
Terpenes solubility in water and their environmental distribution
inferredcites →https://doi.org/10.1016/j.tca.2010.07.023openalex-snapshot
Temperature and composition-dependent properties of the two-component system d- and l-camphor at ‘ordinary’ pressure
inferredcites →https://doi.org/10.1016/j.tca.2018.04.014openalex-snapshot
Dielectric and thermodynamic study of camphor and borneol enantiomers and their binary systems
inferredcites →https://doi.org/10.1016/s0168-3659(97)00153-3openalex-snapshot
Transdermal delivery from eutectic systems: enhanced permeation of a model drug, ibuprofen
inferredcites →https://doi.org/10.1016/s0378-5173(00)00505-6openalex-snapshot
Physicochemical studies of lidocaine–menthol binary systems for enhanced membrane transport
inferredcites →https://doi.org/10.1016/s1808-8694(15)30976-9openalex-snapshot
Pharmaceutical excipients and the information on drug labels
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00571openalex-snapshot
Green and Sustainable Solvents in Chemical Processes
inferredcites →https://doi.org/10.1021/acs.iecr.7b02247openalex-snapshot
Selecting Critical Properties of Terpenes and Terpenoids through Group-Contribution Methods and Equations of State
inferredcites →https://doi.org/10.1021/acssuschemeng.8b01203openalex-snapshot
Tunable Hydrophobic Eutectic Solvents Based on Terpenes and Monocarboxylic Acids
inferredcites →https://doi.org/10.1021/acssuschemeng.8b03520openalex-snapshot
A Search for Natural Hydrophobic Deep Eutectic Solvents Based on Natural Components
inferredcites →https://doi.org/10.1021/cr050989dopenalex-snapshot
Chemical Routes for the Transformation of Biomass into Chemicals
inferredcites →https://doi.org/10.1021/j100007a062openalex-snapshot
Conductor-like Screening Model for Real Solvents: A New Approach to the Quantitative Calculation of Solvation Phenomena
inferredcites →https://doi.org/10.1039/b210714gopenalex-snapshot
Novel solvent properties of choline chloride/urea mixturesElectronic supplementary information (ESI) available: spectroscopic data. See http://www.rsc.org/suppdata/cc/b2/b210714g/
inferredcites →https://doi.org/10.1039/c6gc02191copenalex-snapshot
Solvent from forestry biomass. Pinane a stable terpene derived from pine tree byproducts to substitute n-hexane for the extraction of bioactive compounds
inferredcites →https://doi.org/10.1039/c9cc04846dopenalex-snapshot
Phenolic hydrogen bond donors in the formation of non-ionic deep eutectic solvents: the quest for type V DES
inferredcites →https://doi.org/10.1039/ct9099500590openalex-snapshot
LXXVI.—The miscibility of solids
inferredcites →https://doi.org/10.1208/s12249-015-0459-xopenalex-snapshot
Evaporation Behavior and Characterization of Eutectic Solvent and Ibuprofen Eutectic Solution
inferredcites →https://doi.org/10.1271/bbb.64.731openalex-snapshot
Effects of Branched Cyclodextrins on the Solubility and Stability of Terpenes
inferredcites →https://doi.org/10.1524/zpch.1992.177.part_2.143openalex-snapshot
Hydrogen Bond Donation Properties of Organic Solvents and Their Aqueous Mixtures from 13C NMR Data of Pyridine-N-Oxide
inferredcites →https://doi.org/10.3390/ijms160817101openalex-snapshot
Opportunities for Bio-Based Solvents Created as Petrochemical and Fuel Products Transition towards Renewable Resources
inferredcites →https://doi.org/10.3390/separations6010009openalex-snapshot
Recent Advances in Hydrophobic Deep Eutectic Solvents for Extraction
inferredcites →https://doi.org/10.4172/2329-6631.1000e130openalex-snapshot
Pharmaceutical Applications of Eutectic Mixtures
inferredcites →https://doi.org/10.5897/bmbropenalex-snapshot
Biotechnology and Molecular Biology Reviews

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4069725openalex-extracted
inferred← citeshttps://doi.org/10.1002/aic.17382openalex-snapshot
Molecular dynamics simulations of heterogeneous hydrogen bond environment in hydrophobic deep eutectic solvents
inferred← citeshttps://doi.org/10.1002/aocs.12757openalex-snapshot
Hydrophobic natural deep eutectic solvents for marine lipid extraction
inferred← citeshttps://doi.org/10.1002/cphc.202400768openalex-snapshot
On the Solvation Properties of Menthol‐Thymol Mixtures. A Molecular Dynamics Investigation
inferred← citeshttps://doi.org/10.1002/ejoc.70400openalex-snapshot
A Sustainable Borrowing Hydrogen Strategy in Natural Deep Eutectic Solvents for the N ‐Alkylation of Amines From Alcohols
inferred← citeshttps://doi.org/10.1002/gch2.202000103openalex-snapshot
A Theoretical Study on Terpene‐Based Natural Deep Eutectic Solvent: Relationship between Viscosity and Hydrogen‐Bonding Interactions
inferred← citeshttps://doi.org/10.1002/slct.202405605openalex-snapshot
Enhancing the Solubility of Dihomo‐gamma‐Linolenic Acid Using Natural Deep Eutectic Solvents for Human Tumors Therapy Development
inferred← citeshttps://doi.org/10.1002/tcr.202300267openalex-snapshot
Menthol‐Based (Deep) Eutectic Solvents: A Review on Properties and Application in Extraction
inferred← citeshttps://doi.org/10.1007/s00217-023-04302-0openalex-snapshot
Improving carotenoid extraction, stability, and antioxidant activity from Citrus sinensis peels using green solvents
inferred← citeshttps://doi.org/10.1007/s10953-024-01372-wopenalex-snapshot
Quantum Chemistry-Based Approach for Density Prediction of non-ionic Hydrophobic Eutectic Solvents
inferred← citeshttps://doi.org/10.1007/s13399-026-07195-7openalex-snapshot
Natural deep eutectic solvents (Na)DES as green tools for the valorization of citrus byproducts: advances, challenges and perspectives
inferred← citeshttps://doi.org/10.1016/bs.abr.2020.09.008openalex-snapshot
A look on target-specificity of eutectic systems based on natural bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.cej.2022.138544openalex-snapshot
Extraction of pharmaceuticals from hospital wastewater with eutectic solvents and terpenoids: Computational, experimental, and simulation studies
inferred← citeshttps://doi.org/10.1016/j.cejgas.2025.100016openalex-snapshot
Fenchol- and alpha-terpineol-based eutectic solvents: antimicrobial activities and bixin extraction from annatto mixture
inferred← citeshttps://doi.org/10.1016/j.ces.2025.121245openalex-snapshot
An integrated ML model for the prediction of the melting points, phase diagrams, and eutectic points of the Type III and V deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.cogsc.2022.100612openalex-snapshot
Type V deep eutectic solvents: Design and applications
inferred← citeshttps://doi.org/10.1016/j.ejpb.2023.09.002openalex-snapshot
Thermoresponsive cholesteric liquid–crystal systems doped with terpenoids as drug delivery systems for skin applications
inferred← citeshttps://doi.org/10.1016/j.eng.2023.10.020openalex-snapshot
Machine-Learning-Assisted Design of Deep Eutectic Solvents Based on Uncovered Hydrogen Bond Patterns
inferred← citeshttps://doi.org/10.1016/j.envres.2022.114232openalex-snapshot
Construction of ANbO3 (A= Na, K)/f-carbon nanofiber composite: Rapid and real-time electrochemical detection of hydroxychloroquine in environmental samples
inferred← citeshttps://doi.org/10.1016/j.envres.2022.115207openalex-snapshot
Sustainable recovery of phenolic antioxidants from real olive vegetation water with natural hydrophobic eutectic solvents and terpenoids
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2023.112374openalex-snapshot
Replacing organics with water: Macromolecular engineering of non-water miscible poly(meth)acrylates via interfacial and ion-pair catalysis SARA ATRP in miniemulsion
inferred← citeshttps://doi.org/10.1016/j.fluid.2022.113704openalex-snapshot
Vapor pressures and thermophysical properties of selected monoterpenoids II
inferred← citeshttps://doi.org/10.1016/j.foodchem.2021.131630openalex-snapshot
Carvone and its eutectic mixtures as novel, biodegradable, and tunable solvents to extract hydrophobic compounds in substitution for volatile toxic solvents
inferred← citeshttps://doi.org/10.1016/j.foodchem.2021.131930openalex-snapshot
A priori design of new natural deep eutectic solvent for lutein recovery from microalgae
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.134703openalex-snapshot
Hydrophobic deep eutectic solvents in the food sector: Focus on their use for the extraction of bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.135079openalex-snapshot
Evaluating the status quo of deep eutectic solvent in food chemistry. Potentials and limitations
inferred← citeshttps://doi.org/10.1016/j.foodres.2025.116352openalex-snapshot
Green extractions of bioactive compounds from citrus peels and their applications in the food industry
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.147342openalex-snapshot
Green engineering of polylactic acid/polymyrcene/cellulose nanocrystals films with tunable mechanical and UV-shielding properties for food packaging applications
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117002openalex-snapshot
Optimisation and modelling of ultrasonic-assisted extraction of canthaxanthin from Chromochloris zofingiensis using eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.jclepro.2026.148993openalex-snapshot
A multi-task learning model integrating physical property databases and multidimensional descriptors for predicting thermophysical properties of type III and V deep eutectic solvents and assisting screening
inferred← citeshttps://doi.org/10.1016/j.jece.2021.106128openalex-snapshot
Extractive removal and recovery of bisphenol A from aqueous solutions using terpenoids and hydrophobic eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.jece.2022.108237openalex-snapshot
High-pressure carbon dioxide solubility in terpene based deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.jece.2023.110562openalex-snapshot
Novel approach for azole fungicides extraction from aqueous environments using terpenes and eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.jece.2025.119313openalex-snapshot
Liquid-liquid extraction experiments and molecular mechanism studies based on new deep eutectic solvents for separating biomass derivatives in water
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.130957openalex-snapshot
VOCs absorption from gas streams using deep eutectic solvents – A review
inferred← citeshttps://doi.org/10.1016/j.jiec.2021.03.011openalex-snapshot
Hydrophobic deep eutectic solvents: Current progress and future directions
inferred← citeshttps://doi.org/10.1016/j.jmgm.2022.108152openalex-snapshot
Molecular dynamics investigation of non-ionic deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.microc.2025.112794openalex-snapshot
Development of a ready-to-use astaxanthin esters extract from Haematococcus pluvialis using hydrophobic NADES: Optimization, mechanistic insights, and stability evaluation
inferred← citeshttps://doi.org/10.1016/j.mochem.2026.100038openalex-snapshot
Molecular thermodynamics and solvation design in a hydrophobic menthol:linalool solvent: From physicochemical characterization to β-sitosterol extraction affinity
inferred← citeshttps://doi.org/10.1016/j.molliq.2020.113667openalex-snapshot
Formation of glassy phases and polymorphism in deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.molliq.2020.114834openalex-snapshot
Effect of choline chloride based natural deep eutectic solvents on aqueous solubility and thermodynamic properties of acetaminophen
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.119492openalex-snapshot
Phenol-cyclohexanol eutectic mixtures: Phase diagram and microscopic structure by experimental and computational studies
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120145openalex-snapshot
Dynamics of type V menthol-thymol deep eutectic solvents: Do they reveal non-ideality?
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120582openalex-snapshot
Nonideality and cocrystal formation in l-menthol/xylenol eutectic systems
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120789openalex-snapshot
Thymol+l-menthol eutectic mixtures: Thermophysical properties and possible applications as decontaminants
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.121151openalex-snapshot
Liquid structure of a water-based, hydrophobic and natural deep eutectic solvent: The case of thymol-water. A Molecular Dynamics study
inferred← citeshttps://doi.org/10.1016/j.molliq.2023.121631openalex-snapshot
Molecular insights into potential hydrophobic deep eutectic solvents for furfural extraction guided by COSMO-RS and machine learning
inferred← citeshttps://doi.org/10.1016/j.molliq.2023.121724openalex-snapshot
Thermodynamic study of selected aromatic monoterpenoids
inferred← citeshttps://doi.org/10.1016/j.molliq.2023.121899openalex-snapshot
Database of deep eutectic solvents and their physical properties: A review
inferred← citeshttps://doi.org/10.1016/j.molliq.2023.121918openalex-snapshot
COSMO-RS predictive screening of type 5 hydrophobic deep eutectic solvents for selective platform chemicals absorption
inferred← citeshttps://doi.org/10.1016/j.molliq.2023.122280openalex-snapshot
Is it possible to correlate various physicochemical properties of Natural Deep eutectic systems in order to predict their behaviours as solvents?
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125069openalex-snapshot
Characterization of camphor: thymol or dl-menthol eutectic mixtures; Structure, thermophysical properties, and lidocaine solubility
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125726openalex-snapshot
Terpene-based eutectic mixtures for cutaneous delivery: Eutectic point vs. molar ratio - which matters more?
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.126526openalex-snapshot
Probing the potential of type V Deep eutectic solvents as sustainable electrolytes
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.126591openalex-snapshot
Development of hydrophobic eutectic solvents composed of DL-menthol and fatty acids/alcohols: Application in the extraction of capsaicinoids and carotenoids from Capsicum frutescens
inferred← citeshttps://doi.org/10.1016/j.molliq.2025.127332openalex-snapshot
Design and characterization of novel hydrophobic eutectic solvents based on metal-extracting ligands
inferred← citeshttps://doi.org/10.1016/j.molliq.2025.127676openalex-snapshot
Different impact of menthol chirality on ideal and deep eutectic solvents: Thermal and structural insights
inferred← citeshttps://doi.org/10.1016/j.molliq.2025.128103openalex-snapshot
Phase diagrams of therapeutic deep eutectic solvents (THEDES) under CO2 partial pressure
inferred← citeshttps://doi.org/10.1016/j.molliq.2025.128154openalex-snapshot
Role of gelator concentration in shaping the molecular and macroscopic properties of thymol:camphor supramolecular eutectogels
inferred← citeshttps://doi.org/10.1016/j.mtchem.2023.101402openalex-snapshot
Hydrophobic eutectogels: a new outfit for non-ionic eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.mtchem.2025.102535openalex-snapshot
The effect of increasing water on the physicochemical features of thymol: DL-menthol based natural deep eutectic solvent (DES)
inferred← citeshttps://doi.org/10.1016/j.polymer.2022.124586openalex-snapshot
L-menthol and thymol eutectic mixture as a bio-based solvent for the “one-pot” synthesis of well-defined amphiphilic block copolymers by ATRP
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2023.107791openalex-snapshot
Bioactive surfaces with well-defined amphiphilic copolymers containing a natural terpene-based monomer
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103861openalex-snapshot
Efficient ball milling assisted approach to recover lutein from microalgae biomass with natural deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.rser.2021.111986openalex-snapshot
Lignin fractionation from lignocellulosic biomass using deep eutectic solvents and its valorization
inferred← citeshttps://doi.org/10.1016/j.sampre.2023.100086openalex-snapshot
Capillary electrophoresis instrumentation for determination of viscosity of deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.seppur.2020.117379openalex-snapshot
Separation of phenols from aqueous streams using terpenoids and hydrophobic eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.seppur.2021.120117openalex-snapshot
Extraction of antibiotics identified in the EU Watch List 2020 from hospital wastewater using hydrophobic eutectic solvents and terpenoids
inferred← citeshttps://doi.org/10.1016/j.seppur.2022.122148openalex-snapshot
Extraction of neonicotinoid pesticides from aquatic environmental matrices with sustainable terpenoids and eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.seppur.2023.123129openalex-snapshot
Experimental study on CO2 separation using hydrophobic deep eutectic solvent based supported liquid membranes
inferred← citeshttps://doi.org/10.1016/j.seppur.2023.124524openalex-snapshot
Flow-based recovery of acetic acid from aqueous solutions using bio-derived terpenes as extracting solvents
inferred← citeshttps://doi.org/10.1016/j.seppur.2024.130583openalex-snapshot
New family of type V natural hydrophobic deep eutectic solvents based on thymol-acetamide/acetanilide: Characteristics, intermolecular interactions and applications in liquid–liquid extraction
inferred← citeshttps://doi.org/10.1016/j.seppur.2025.133278openalex-snapshot
Using COSMO-RS in the designing and screening of different eutectic solvents for the extraction of carbaryl
inferred← citeshttps://doi.org/10.1016/j.seppur.2025.133930openalex-snapshot
Mechanistic insights into highly efficient rare earth extraction using promising novel trioctylphosphine oxide-based deep eutectic solvents
inferred← citeshttps://doi.org/10.1016/j.seppur.2025.134130openalex-snapshot
Investigation of renewable solvents for the extraction of aromatic acids
inferred← citeshttps://doi.org/10.1016/j.talanta.2023.125599openalex-snapshot
Critical overview on the use of hydrophobic (deep) eutectic solvents for the extraction of organic pollutants in complex matrices
inferred← citeshttps://doi.org/10.1016/j.trac.2021.116187openalex-snapshot
Emerging applications of (micro) extraction phase from hydrophilic to hydrophobic deep eutectic solvents: opportunities and trends
inferred← citeshttps://doi.org/10.1016/j.trac.2024.117752openalex-snapshot
Atypical deep eutectic solvents: New opportunities for chemical analysis
inferred← citeshttps://doi.org/10.1016/s0065-2296(21)00010-0openalex-snapshot
Preface: Natural deep eutectic solvents: A third liquid phase in living organisms? Discovery, theory, biology, and applications
inferred← citeshttps://doi.org/10.1021/acs.analchem.5c01641openalex-snapshot
Eutectic Point Determination of Type V Hydrophobic Octanoic Acid-Based Solvents by “Lock-Free” 1H and 13C NMR Self-Diffusion Experiments
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c00306openalex-snapshot
Experimental Investigation and Modeling of Cocrystal Formation in L-Menthol/Thymol Eutectic System
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c01477openalex-snapshot
Cocrystal Formation in Choline Chloride Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c01081openalex-snapshot
Thymol–Menthol Deep Eutectic Solvents and Eutectogels as Pharmaceutical Crystallization Media
inferred← citeshttps://doi.org/10.1021/acs.iecr.3c00054openalex-snapshot
Bridging Machine Learning and Redlich–Kister Theory for Solid–Liquid Equilibria Prediction of Binary Eutectic Solvent Systems
inferred← citeshttps://doi.org/10.1021/acs.iecr.3c01063openalex-snapshot
Estimating the Melting Temperatures of Type V Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.1021/acs.iecr.5c01348openalex-snapshot
Hybrid Approach for Predicting Melting Points in Nonionic Eutectic Solvents Using Thermodynamics and Machine Learning
inferred← citeshttps://doi.org/10.1021/acs.iecr.6c01577openalex-snapshot
Terpene-Based Eutectic Mixtures as Green Solvents for CO 2 Capture: Experimental Characterization and Molecular Insights
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c00676openalex-snapshot
Deep Eutectic Solvent-Assisted Synthesis of a Strontium Tungstate Bifunctional Catalyst: Investigation on the Electrocatalytic Determination and Photocatalytic Degradation of Acetaminophen and Metformin Drugs
inferred← citeshttps://doi.org/10.1021/acs.jced.2c00495openalex-snapshot
Water Miscibility, Surface Tension, Density, and Dynamic Viscosity of Hydrophobic Deep Eutectic Solvents Composed of Capric Acid, Menthol, and Thymol
inferred← citeshttps://doi.org/10.1021/acs.jced.6c00043openalex-snapshot
Solid-Phase Equilibria of Thymol- and Carvacrol-Based Hydrophobic Eutectic Solvents with Fatty Chains and Their Application to Carotenoid Extraction
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01138openalex-snapshot
Revival of Thermal Aziridine–Alkene Cycloaddition: Pyrrolidine Synthesis in Terpenoid-Based Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.1021/acs.jpcb.0c02386openalex-snapshot
Liquefying Compounds by Forming Deep Eutectic Solvents: A Case Study for Organic Acids and Alcohols
inferred← citeshttps://doi.org/10.1021/acs.jpcb.5c01154openalex-snapshot
Revealing Solvation within [ l (−)-Menthol : Thymol] Deep Eutectic Solvents via Microfluidity Assessment
inferred← citeshttps://doi.org/10.1021/acs.jpcb.6c00485openalex-snapshot
Revealing Temperature-Dependent Dynamic Crossover of Molecular Solutes in Thymol–Camphor-Based Type V Deep Eutectic Solvent via Optical Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.jpcb.6c04073openalex-snapshot
Persistent Menthol Hydrogen-Bonding Networks Govern the Structure and Hydration of a Hydrophobic Natural Deep Eutectic Solvent: Insights from NMR and Molecular Dynamics Simulations of the Camphor–Menthol System
inferred← citeshttps://doi.org/10.1021/acsabm.5c01459openalex-snapshot
Emulsion Gel Packaging System with Sustained Release and Synergistic Antibacterial for Prolonging Fruit and Vegetable Preservation
inferred← citeshttps://doi.org/10.1021/acsapm.3c01673openalex-snapshot
Green Synthesis and Characterization of Polymyrcene as an Oxygen Scavenging Sustainable Polymer for Active Food Packaging Applications
inferred← citeshttps://doi.org/10.1021/acsmaterialslett.3c00938openalex-snapshot
Hydrophobic Eutectogels as Electrodes for Underwater Electromyography Recording
inferred← citeshttps://doi.org/10.1021/acsomega.3c03326openalex-snapshot
Molecular Guide for Selecting Green Deep Eutectic Solvents with High Monosaccharide Solubility for Food Applications
inferred← citeshttps://doi.org/10.1021/acsomega.5c07390openalex-snapshot
Hydrophobic Eutectic Solvents for Sustainable Bisphenol A Extraction from Water: Screening and Selection Based on Key Performance Criteria
inferred← citeshttps://doi.org/10.1021/acspolymersau.5c00114openalex-snapshot
Reversible Deactivation Radical Polymerization in Biomass-Derived Solvents: Sustainable Approach in Polymer Chemistry
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c00559openalex-snapshot
The Curious Case of Hydrophobic Deep Eutectic Solvents: A Story on the Discovery, Design, and Applications
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c05518openalex-snapshot
Eutectic Mixtures Based on Polyalcohols as Sustainable Solvents: Screening and Characterization
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c07874openalex-snapshot
Non-Ideality in Thymol + Menthol Type V Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.1021/acssuschemeng.1c02798openalex-snapshot
Sustainable Production of Furfural in Biphasic Reactors Using Terpenoids and Hydrophobic Eutectic Solvents
inferred← citeshttps://doi.org/10.1021/acssuschemeng.1c04591openalex-snapshot
Evaluation of Deep Eutectic Systems as an Alternative to Solvents in Painting Conservation
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c00293openalex-snapshot
Assessing the Temperature-Dependent Tunable Polarity of N , N -Dimethylcyclohexylamine (DMCHA) and Water Mixtures
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c00920openalex-snapshot
Structural Study of a Eutectic Solvent Reveals Hydrophobic Segregation and Lack of Hydrogen Bonding between the Components
inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c01209openalex-snapshot
The Complex Story Behind a Deep Eutectic Solvent Formation as Revealed by l -Menthol Mixtures with Butylated Hydroxytoluene Derivatives
inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c02997openalex-snapshot
Unveiling the Use of Hydrophobic Eutectic Solutions as Task-Specific Solvents To Recover Bacterioruberin from Haloferax mediterranei
inferred← citeshttps://doi.org/10.1021/acssuschemeng.4c04061openalex-snapshot
Criteria for a Critical Selection of Hydrophobic (Deep) Eutectic Mixtures
inferred← citeshttps://doi.org/10.1038/s41598-026-47313-zopenalex-snapshot
Potential of sustainable, ecofriendly sterol derivatives as additives for water and oil repellency
inferred← citeshttps://doi.org/10.1039/d0gc00793eopenalex-snapshot
Non-ionic hydrophobic eutectics – versatile solvents for tailored metal separation and valorisation
inferred← citeshttps://doi.org/10.1039/d0gc03077eopenalex-snapshot
Predicting the density and viscosity of hydrophobic eutectic solvents: towards the development of sustainable solvents
inferred← citeshttps://doi.org/10.1039/d1cp04509aopenalex-snapshot
Nanostructuring and macroscopic behavior of type V deep eutectic solvents based on monoterpenoids
inferred← citeshttps://doi.org/10.1039/d2gc03558hopenalex-snapshot
From non-conventional ideas to multifunctional solvents inspired by green chemistry: fancy or sustainable macromolecular chemistry?
inferred← citeshttps://doi.org/10.1039/d3cp01207gopenalex-snapshot
Fluorescence of pyrene and its derivatives to reveal constituent and composition dependent solvation within hydrophobic deep eutectic solvents
inferred← citeshttps://doi.org/10.1039/d3nj00228dopenalex-snapshot
Sustainable solutions for removing aged wax-based coatings from cultural heritage: exploiting hydrophobic deep eutectic solvents (DESs)
inferred← citeshttps://doi.org/10.1039/d4an01161aopenalex-snapshot
Development of essential oil diffusion matrices using non-ionic surfactants-supported NADES and hydrophobic NADES
inferred← citeshttps://doi.org/10.1039/d4fd00083hopenalex-snapshot
Exploring the structure of type V deep eutectic solvents by xenon NMR spectroscopy
inferred← citeshttps://doi.org/10.1039/d5gc00489fopenalex-snapshot
Examining the potential of type V DESs for the solvent extraction of metal ions
inferred← citeshttps://doi.org/10.1063/5.0080470openalex-snapshot
Insights on novel type V deep eutectic solvents based on levulinic acid
inferred← citeshttps://doi.org/10.1080/02773813.2023.2299814openalex-snapshot
Surface analysis of different wood polymer composites exposed to artificial weathering
inferred← citeshttps://doi.org/10.1080/17518253.2021.2009579openalex-snapshot
New natural deep eutectic solvents based on aromatic organic acids
inferred← citeshttps://doi.org/10.1134/s0006297923140092openalex-snapshot
Deep Eutectic Solvents for Biotechnology Applications
inferred← citeshttps://doi.org/10.1146/annurev-chembioeng-101121-085323openalex-snapshot
Everything You Wanted to Know about Deep Eutectic Solvents but Were Afraid to Be Told
inferred← citeshttps://doi.org/10.1515/cppm-2020-0119openalex-snapshot
Phase equilibria modeling of biorefinery-related systems: a systematic review
inferred← citeshttps://doi.org/10.1590/1519-6984.290536openalex-snapshot
Schinus terebinthifolius Raddi essential oil: chemical composition and action on the quality of bean grains
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-pd0tgopenalex-snapshot
Deciphering Hydrogen Bond Features to Develop Machine Learning Models for Predicting Non-ionic Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.3390/ijms26030997openalex-snapshot
The Single-Parameter Bragg–Williams Model for Eutectic Solvents
inferred← citeshttps://doi.org/10.3390/molecules25010210openalex-snapshot
Extraction of High Value Triterpenic Acids from Eucalyptus globulus Biomass Using Hydrophobic Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.3390/molecules26144208openalex-snapshot
Influence of the Molecular Structure of Constituents and Liquid Phase Non-Ideality on the Viscosity of Deep Eutectic Solvents
inferred← citeshttps://doi.org/10.3390/molecules27196210openalex-snapshot
Design of Deep Eutectic Systems: Plastic Crystalline Materials as Constituents
inferred← citeshttps://doi.org/10.3390/molecules29174232openalex-snapshot
Characterization of Camphene- and Fenchol-Based Hydrophobic Eutectic Solvents and Their Application in Aldehyde Extraction
inferred← citeshttps://doi.org/10.3390/pr12061255openalex-snapshot
Hydrophobic Deep Eutectic Solvents for Ethanol, Propan-1-ol, and Propan-2-ol Recovery from Aqueous Solutions
inferred← citeshttps://doi.org/10.3390/pr14071109openalex-snapshot
Sustainable Valorization of Spent Coffee Grounds: Phenolic Compound Extraction Using Hydrophobic Eutectic Solvents
inferred← citeshttps://doi.org/10.3390/pr8101220openalex-snapshot
A Review of the Use of Eutectic Solvents, Terpenes and Terpenoids in Liquid–liquid Extraction Processes
inferred← citeshttps://doi.org/10.3390/separations12080214openalex-snapshot
Hydrophobic Natural Deep Eutectic Solvents for Extraction of Bioactive Compounds: Multiscale Characterization, Quantum Simulations, and Molecular Interaction Studies with Cry j 1 and Amb a 1 Allergens
inferred← citeshttps://doi.org/10.59761/rcr5190openalex-snapshot
Bio-derived oils and their derivatives as renewable-green solvents in organic synthesis
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.