TargetMol

Lilial

Product Code:
 
TAR-T20741
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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CodeSizePrice
TAR-T20741-5mg5mg£111.00
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Quantity:
TAR-T20741-1mL1 mL * 10 mM (in DMSO)£117.00
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Quantity:
TAR-T20741-10mg10mg£131.00
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Quantity:
TAR-T20741-25mg25mg£173.00
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Quantity:
TAR-T20741-50mg50mg£225.00
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Quantity:
TAR-T20741-100mg100mg£301.00
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Quantity:
TAR-T20741-200mg200mg£417.00
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Quantity:
TAR-T20741-500mg500mg£643.00
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Quantity:
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This product comes from: United States.
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Further Information

Bioactivity:
Lilial (a trade name for lily aldehyde, also known as lysmeral) is a chemical compound commonly used as a perfume in cosmetic preparations and laundry powders, often under the name butylphenyl methylpropional. It is a synthetic aromatic aldehyde.Lilial is a high-tonnage perfumery ingredient with an odour of lily-of-the-valley. It is a CMR2 material.
CAS:
80-54-6
Formula:
C14H20O
Molecular Weight:
204.313
Purity:
0.95
SMILES:
CC(Cc1ccc(cc1)C(C)(C)C)C=O

References

1. Schroeder M, Mathys M, Ehrensperger N, B?chel M. ?-Unsaturated aldehydes as potential Lilial replacers. Chem Biodivers. 2014 Oct;11(10):1651-73. doi: 10.1002/cbdv.201400072. PubMed PMID: 25329790. 2. Usta J, Hachem Y, El-Rifai O, Bou-Moughlabey Y, Echtay K, Griffiths D, Nakkash-Chmaisse H, Makki RF. Fragrance chemicals lyral and lilial decrease viability of HaCat cells' by increasing free radical production and lowering intracellular ATP level: protection by antioxidants. Toxicol In Vitro. 2013 Feb;27(1):339-48. doi: 10.1016/j.tiv.2012.08.020. Epub 2012 Aug 24. PubMed PMID: 22940465. 3. Esmaeili A, Afshari S, Esmaeili D. Formation of harmful compounds in biotransformation of lilial by microorganisms isolated from human skin. Pharm Biol. 2015;53(12):1768-73. doi: 10.3109/13880209.2015.1005755. Epub 2015 Apr 9. PubMed PMID: 25856710. 4. Stueckler C, Mueller NJ, Winkler CK, Glueck SM, Gruber K, Steinkellner G, Faber K. Bioreduction of alpha-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial and Helional. Dalton Trans. 2010 Sep 28;39(36):8472-6. doi: 10.1039/c002971h. Epub 2010 May 11. PubMed PMID: 20461254.