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135178

Sigma-Aldrich

Cuminaldehyd

98%

Synonym(e):

4-Isopropyl-benzaldehyd

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About This Item

Lineare Formel:
(CH3)2CHC6H4CHO
CAS-Nummer:
122-03-2
Molekulargewicht:
148.20
Beilstein:
636547
EG-Nummer:
204-516-9
MDL-Nummer:
MFCD00006953
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24848203

Qualitätsniveau

100

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.529 (lit.)

bp

235-236 °C (lit.)

Löslichkeit

H2O: insoluble
alcohol: soluble
diethyl ether: soluble

Dichte

0.981 g/mL at 20 °C
0.977 g/mL at 25 °C (lit.)

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

InChIKey

WTWBUQJHJGUZCY-UHFFFAOYSA-N

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Anwendung

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. Wirkung

Cuminaldehyde increases the insulin secretion in streptozotocin-induced diabetic rats. It suppresses melanin formation in cultured murine B16-F10 melanoma cells.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

199.4 °F

Flammpunkt (°C)

93 °C

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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4-Ethoxybenzaldehyd 99%

Sigma-Aldrich

173606

4-Ethoxybenzaldehyd

Eugenol ReagentPlus®, 99%

Sigma-Aldrich

E51791

Eugenol

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)
Hoi-Seon Lee
Journal of agricultural and food chemistry, 53(7), 2446-2450 (2005-03-31)
The inhibitory activity of Cuminum cyminum seed-isolated component was evaluated against lens aldose reductase and alpha-glucosidase isolated from Sprague-Dawley male rats and compared to that of 11 commercially available components derived from C. cyminum seed oil, as well as quercitrin
Teruhiko Nitoda et al.
Phytotherapy research : PTR, 22(6), 809-813 (2008-04-17)
Cuminaldehyde (4-isopropylbenzaldehyde) suppressed melanin formation in cultured murine B16-F10 melanoma cells in a dose-dependent decrease up to 0.25 mm without affecting cell growth. Approximately 30% suppression in melanin production resulted when the cells were cultured with 0.25 mm of cuminaldehyde.
M Désage et al.
Journal of chromatography. B, Biomedical applications, 678(2), 205-210 (1996-04-12)
The flavours contained in a mammalian mother's milk can exert a marked influence on her offspring's proximate suckling behaviour and later preferences. The aim of this study was to establish a reliable analytical procedure to characterise the mammary transfer of
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