Results 61 to 70 of about 2,540 (232)

Influence of chemical structure on absolute odour thresholds and odour characteristics of ortho- and para-halogenated phenols and cresols [PDF]

open access: yes, 2022
S.304-312Halogenated phenols and cresols belong to a group of volatiles consistently reported as off-flavour compounds. For example, 2-iodophenol and 2-iodo-4-methylphenol with their typical medicinal smell were found to negatively affect bottled mineral
Czerny, Michael   +2 more
core   +1 more source

Recent advances in polymeric chemically amplified positive resists: Materials and design strategies

open access: yesSmart Molecules, EarlyView.
This review summarizes recent advances in the molecular design of positive chemically amplified resists, focusing on photoacid generators and polymer architectures. Key strategies for enhancing sensitivity—including self‐amplification effects, copolymerization of sensitive monomers, controlled polymerization, and photosensitized chemically amplified ...
Litao Zhou   +3 more
wiley   +1 more source

Adsorption of cresols on molybdenite [PDF]

open access: yes, 1972
A spectrophotometric method has been developed to determine individual cresols as well as mixed cresol isomers. The cresols were determined by the yellow colour produced by nitrocresols in an alkaline medium. The optimum wavelength was found to be at 395
Viswanathan, K V, Majumdar, K K
core  

Pyrolyse thermique des [14C] et [3H] ortho et para-cresols [PDF]

open access: yes, 1975
The thermal cracking of ortho and para-cresols labelled in specific position with [14C] and [3H] shows that the formation of water and methane are directly related to the formation of toluene and phenol respectively.
R. Cypres   +3 more
core   +1 more source

Kinetic study for ionic liquid catalyzed green O-methylation of cresols using dimethyl carbonate [PDF]

open access: yes, 2021
In this work, we have systematically studied the kinetics and mechanism of ionic liquid catalyzed solvent less liquid-phase O-methylation of p-cresol with dimethyl carbonate (DMC).
Jain, Suresh S., Yadav, Ganapati D.
core   +1 more source

Diet–Microbiome–Immune Interactions at the Gut Mucosa in Food Allergy: Mechanisms, Gaps, and Therapeutic Implications

open access: yesAllergy, EarlyView.
ABSTRACT Mucosal surfaces are sites of highly dynamic interactions among epithelial and immune cells, environmental exposures, particularly dietary inputs, and the diverse microbial communities and their metabolites. These elements continually influence each other to maintain homeostasis and ensure appropriate immune discrimination between pathogens ...
Clara Delaroque   +5 more
wiley   +1 more source

Kinetic Study of the Electrochemical Mineralization of m-Cresol on a Boron-Doped Diamond Anode. [PDF]

open access: yes, 2012
The kinetics of the electrooxidation of m-cresol in aqueous solution was investigated in a one-compartment flow electrochemical cell with a boron-doped diamond electrode (BDD).
Flox, Cristina   +3 more
core   +1 more source

A New Highly Concentrated Insulin Aspart AT278 (500 U/mL) Demonstrates Ultra‐Rapid Pharmacokinetic and Pharmacodynamic Properties in Type 2 Diabetes Regardless of BMI

open access: yesDiabetes, Obesity and Metabolism, EarlyView.
ABSTRACT Aims To evaluate the pharmacokinetics, pharmacodynamics, and safety of a novel U500 insulin aspart formulation (AT278 [500 U/mL]; AT278‐U500) compared with standard concentration insulin aspart (InsAsp [100 U/mL]; InsAsp‐U100) and U500 human regular insulin (HumIns [500 IU/mL]; HumIns‐U500). Materials and Methods This single‐centre, randomised,
Eva Svehlikova   +11 more
wiley   +1 more source

Synthesis of cresols and xylenols from benzene and methanol [PDF]

open access: yes, 1992
The objective of the work is to compare two processes for manufacturing cresols and xylenols: (1) a conventional catalytic process, and (2) a photo-thermal catalytic process, in order to determine the relative process economics.
Alam, S.   +2 more
core   +1 more source

Lipase catalyzed esterification of cresols. [PDF]

open access: yes, 2002
Esters of m- and p-cresols with organic acids having carbon chain lengths C2-C18 have been prepared by using lipases from porcine pancreas and Rhizomucor miehei.
Divakar, S.   +2 more
core   +2 more sources

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