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Vanillylacetone - 97%,flavors and fragrances, high purity , CAS No.122-48-5
Basic Description
Synonyms
(0)-Paradol | EN300-1721864 | HMS3651E22 | Vanillyl acetone | SCHEMBL119051 | EINECS 204-548-3 | Tox21_302493 | ZINGERONE | Zingiberone | SY017980 | AS-65368 | UNII-4MMW850892 | Vanillylacetone, >=98%, natural, FG | [0]Paradol | [0]-Paradol | DB15589 | 4-
Specifications & Purity
≥97%, flavors and fragrances
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Phenols
Subclass
Methoxyphenols
Intermediate Tree Nodes
Not available
Direct Parent
Methoxyphenols
Alternative Parents
Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Ketones Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Methoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Monocyclic benzene moiety - Ketone - Ether - Organic oxygen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
External Descriptors
Zingiber derived compounds
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488183132
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488183132
IUPAC Name
4-(4-hydroxy-3-methoxyphenyl)butan-2-one
INCHI
InChI=1S/C11H14O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h5-7,13H,3-4H2,1-2H3
InChIKey
OJYLAHXKWMRDGS-UHFFFAOYSA-N
Smiles
CC(=O)CCC1=CC(=C(C=C1)O)OC
Isomeric SMILES
CC(=O)CCC1=CC(=C(C=C1)O)OC
WGK Germany
2
RTECS
EL8900000
PubChem CID
31211
Molecular Weight
194.23
Beilstein
8(4)1866
Reaxy-Rn
2051099
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Refractive Index
1.541
Flash Point(°C)
113 °C
Boil Point(°C)
141°C
Melt Point(°C)
40-41°C
Molecular Weight
194.230 g/mol
XLogP3
0.800
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
4
Exact Mass
194.094 Da
Monoisotopic Mass
194.094 Da
Topological Polar Surface Area
46.500 Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
191.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Chunjing Guo, Wei Zhang, Qiaoyun Zhang, Yanguo Su, Xiaoya Hou, Qiang Chen, Huimin Guo, Ming Kong, Daquan Chen.
(2023)
Novel dual CAFs and tumour cell targeting pH and ROS dual sensitive micelles for targeting delivery of paclitaxel to liver cancer.
Artificial Cells Nanomedicine and Biotechnology,
51
(1):
(170-179).
2.
Wenhua Ji, Xiuli Ma, Jinghua Zhang, Hongkai Xie, Feng Liu, Xiao Wang.
(2015)
Preparation of the high purity gingerols from ginger by dummy molecularly imprinted polymers.
JOURNAL OF CHROMATOGRAPHY A,
1387
(24).
3.
Sirong Huang, Xintong Yao, Boya Cao, Na Zhang, Olugbenga P. Soladoye, Yuhao Zhang, Yu Fu.
(2024)
Encapsulation of zingerone by self-assembling peptides derived from fish viscera: Characterization, interaction and effects on colon epithelial cells.
Food Chemistry-X,
22
(101506).
4.
Huimin Xu, Linghua Piao, Xuanri Shen, Xiande Liu.
(2024)
Zingerone enhances the antitumor activity of attenuated Salmonella-mediated cancer immunotherapy by promoting tumor infiltration by host immune cells.
Journal of Functional Foods,
114
(106017).
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