Insights into the Photodegradation of the Contact Allergen Fragrance Cinnamyl Alcohol: Kinetics, Mechanism, and Toxicity

2021 ◽  
Author(s):  
Junji Wu ◽  
Yanpeng Gao ◽  
Teng Guo ◽  
Na Luo ◽  
Guiying Li ◽  
...  
Keyword(s):  
Cinnamyl Alcohol ◽  
Contact Allergen

Nickel Named Contact Allergen of the Year

2008 ◽  
Vol 39 (2) ◽  
pp. 1-48
Author(s):  
DOUG BRUNK
Keyword(s):  
Contact Allergen

New Online System Offers Contact Allergen Database

2011 ◽  
Vol 41 (6) ◽  
pp. 48
Author(s):  
DAMIAN McNAMARA
Keyword(s):  
Online System ◽  
Contact Allergen

Liquid Phase Aerobic Oxidation of Cinnamyl Alcohol to Cinnamaldehyde: Effect of Different Solvents

2016 ◽  
Vol 5 (3) ◽  
pp. 236-243
Author(s):  
Saddam Hussain ◽  
Mohammad Sadiq
Keyword(s):  
Liquid Phase ◽  
Aerobic Oxidation ◽  
Cinnamyl Alcohol

scholarly journals ZnBr2 Mediated C‐N Bond Formation using Cinnamyl Alcohol and 2‐Amino Pyridines

2021 ◽  
Author(s):  
Ahwan Panigrahi ◽  
Mahadev Sharanappa Sherikar ◽  
Kandikere Ramaiah Prabhu
Keyword(s):  
Bond Formation ◽  
Cinnamyl Alcohol

The Preparation of Specifically Deuterated trans- Cinnamyl Alcohol and trans- Cinnamic Acid

1973 ◽  
Vol 51 (13) ◽  
pp. 2102-2104 ◽  
Author(s):  
Donald G. Lee ◽  
James R. Brownridge
Keyword(s):  
Cinnamic Acid ◽  
Triple Bond ◽  
Lithium Aluminum Hydride ◽  
Aluminum Hydride ◽  
Lithium Aluminum ◽  
Cinnamyl Alcohol ◽  
Partial Reduction ◽  
Work Up

The reduction of ethyl phenylpropiolate by lithium aluminum hydride results in partial reduction of the triple bond to give trans-cinnamyl alcohol. If ethyl phenylpropiolate is reduced by LiAlD4 followed by work-up with acetone and H2O the product is the specifically labeled compound, trans-3-phenyl-2-propen-1-ol-1,1,2-d3. If the ester is reduced with LiAlH4 followed by work-up with acetone-d6 and D2O the product is trans-3-phenyl-2-propen-1-ol-O,3-d2. Oxidation of these two products by sodium ruthenate leads to formation of trans-cinnamic acid-α-d and trans-cinnamic acid-β-d, respectively.

Catalytic oxidation of cinnamyl alcohol using Au–Ag nanotubes investigated by surface-enhanced Raman spectroscopy

Nanoscale ◽  
2015 ◽  
Vol 7 (18) ◽  
pp. 8536-8543 ◽  
Author(s):  
Jean Claudio Santos Costa ◽  
Paola Corio ◽  
Liane Marcia Rossi
Keyword(s):  
Raman Spectroscopy ◽  
Catalytic Oxidation ◽  
Surface Enhanced Raman Spectroscopy ◽  
Cinnamyl Alcohol ◽  
Surface Enhanced ◽  
Surface Enhanced Raman

Carbon Dioxide-Expanded Liquid Substrate Phase: An Effective Medium for Selective Hydrogenation of Cinnamaldehyde to Cinnamyl Alcohol.

ChemInform ◽  
2005 ◽  
Vol 36 (12) ◽  
Author(s):  
Fengyu Zhao ◽  
Shin-ichio Fujita ◽  
Jianmin Sun ◽  
Yutaka Ikushima ◽  
Masahiko Arai
Keyword(s):  
Carbon Dioxide ◽  
Selective Hydrogenation ◽  
Effective Medium ◽  
Cinnamyl Alcohol

Sodium metabisulfite as a contact allergen - an example of a rare chemical mechanism for protein modification

2012 ◽  
Vol 66 (3) ◽  
pp. 123-127 ◽  
Author(s):  
David W. Roberts ◽  
David Basketter ◽  
Ian Kimber ◽  
Jonathan White ◽  
John McFadden ◽  
...  
Keyword(s):  
Protein Modification ◽  
Chemical Mechanism ◽  
Sodium Metabisulfite ◽  
Contact Allergen
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