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线性分子式:
(CH3)2CHC6H4CHO
化学文摘社编号:
分子量:
148.20
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-516-9
Beilstein/REAXYS Number:
636547
MDL number:
InChI key
WTWBUQJHJGUZCY-UHFFFAOYSA-N
InChI
1S/C10H12O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-8H,1-2H3
SMILES string
[H]C(=O)c1ccc(cc1)C(C)C
grade
analytical standard
assay
≥97.0% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.529 (lit.), n20/D 1.531
bp
235-236 °C (lit.)
density
0.981 g/mL at 20 °C, 0.977 g/mL at 25 °C (lit.)
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
Quality Level
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General description
Cuminaldehyde is a constituent of cumin oil that exhibits strong antifungal and antibacterial activities.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
199.4 °F
flash_point_c
93 °C
A quantitative structure?antifungal activity relationship study of oxygenated aromatic essential oil compounds using data structuring and PLS regression analysis
Voda K, et al.
Journal of Molecular Modeling, 10(1), 76-84 (2004)
Valério Monteiro-Neto et al.
PloS one, 15(5), e0232987-e0232987 (2020-05-15)
Escherichia coli and Staphylococcus aureus are important agents of urinary tract infections that can often evolve to severe infections. The rise of antibiotic-resistant strains has driven the search for novel therapies to replace the use or act as adjuvants of
Seed Spices: Production, Quality, Export (2001)
Natural Food Flavors and Colorants (2017)
Annemieke Strijkstra et al.
Applied and environmental microbiology, 80(24), 7592-7603 (2014-09-28)
The betaproteobacteria "Aromatoleum aromaticum" pCyN1 and "Thauera" sp. strain pCyN2 anaerobically degrade the plant-derived aromatic hydrocarbon p-cymene (4-isopropyltoluene) under nitrate-reducing conditions. Metabolite analysis of p-cymene-adapted "A. aromaticum" pCyN1 cells demonstrated the specific formation of 4-isopropylbenzyl alcohol and 4-isopropylbenzaldehyde, whereas with
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