Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(CH3)2CHC6H4CHO
CAS Number:
Molecular Weight:
148.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-516-9
Beilstein/REAXYS Number:
636547
MDL number:
Assay:
98%
Form:
liquid
Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.529 (lit.)
bp
235-236 °C (lit.)
solubility
H2O: insoluble, alcohol: soluble, diethyl ether: soluble
density
0.981 g/mL at 20 °C, 0.977 g/mL at 25 °C (lit.)
functional group
aldehyde
SMILES string
[H]C(=O)c1ccc(cc1)C(C)C
InChI
1S/C10H12O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-8H,1-2H3
InChI key
WTWBUQJHJGUZCY-UHFFFAOYSA-N
Application
Cuminaldehyde has been used to study larvicidal and adulticidal toxicity of monoterpenes against Culex pipiens. It has been used in evaluation of chemical composition, antimicrobial and antioxidant activities of essential oil and various extracts of Eucalyptus gilii.
Biochem/physiol Actions
Cuminaldehyde increases the insulin secretion in streptozotocin-induced diabetic rats. It suppresses melanin formation in cultured murine B16-F10 melanoma cells.
Still not finding the right product?
Explore all of our products under Cuminaldehyde
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
199.4 °F
flash_point_c
93 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Dorsaf Ben Hassine et al.
Molecules (Basel, Switzerland), 17(8), 9540-9558 (2012-08-11)
In this study, essential oil and various extracts (hexane, petroleum ether, acetone, ethanol, methanol and water) of Eucalyptus gilii were screened for their chemical composition, antimicrobial and antioxidant activities. The essential oil chemical composition was analyzed by gas chromatography-mass spectrometry
LARVICIDAL, ADULTICIDAL AND GROWTH INHIBITORY EFFECTS OF MONOTERPENES ON CULEX PIPIENS L.(DIPTERA: CULICIDAE).
Zahran HE-DM, et al.
Journal of Agricultural Research Kafer El-Sheikh Univ, 36(4), 385-341 (2010)
T P Krishnakantha et al.
Indian journal of biochemistry & biophysics, 30(2), 133-134 (1993-04-01)
Effect of spice principles on scavenging of superoxide anion has been investigated. The superoxide anions, as measured by nitrobluetetrazolium (NBT) reduction in xanthine-xanthine oxidase system, were inhibited by superoxide dismutase, spice principles eugenol (cloves) and cuminaldehyde (cumin), antioxidants, butylated hydroxy
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 135178-100G | 04061838730510 |
| 135178-5G | 04061838730527 |
