trans-Anethole
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trans-Anethole
structure -
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CAS No:
4180-23-8
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Formula:
C10H12O
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Chemical Name:
trans-Anethole
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Synonyms:
Benzene,1-methoxy-4-(1E)-1-propen-1-yl-;Anisole,p-propenyl-,(E)-;Benzene,1-methoxy-4-(1-propenyl)-,(E)-;Benzene,1-methoxy-4-(1E)-1-propenyl-;1-Methoxy-4-(1E)-1-propen-1-ylbenzene;trans-Anethole;trans-Anethol;trans-1-(p-Methoxyphenyl)propene;trans-1-(4-Methoxyphenyl)-1-propene;trans-p-Methoxy-β-methylstyrene;(E)-Anethole;trans-p-Anethole;(E)-1-(4-Methoxyphenyl)propene;trans-1-(p-Methoxyphenyl)-1-propene;trans-4-(1-Propenyl)anisole;trans-1-p-Anisylpropene;(E)-1-p-Methoxyphenylpropene;(E)-Anethol;1-Methoxy-4-[(1E)-1-propenyl]benzene;NSC 209529;(E)-1-Methoxy-4-(prop-1-en-1-yl)benzene;109957-71-3;57131-42-7
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CAS No:
Description
Trans-Anethole ((E)-Anethole), a phenylpropene derivative isolated from Pimpinella, shows estrogenic activity at lower concentrations and cytotoxic at higher concentrations in cancer cell lines[1][2]. Trans-Anethole ((E)-Anethole) contributes a large component of the odor and flavor of anise and fennel, anise myrtle, liquorice, camphor, magnolia blossoms, and star anise[3].
Characteristics
9.2
3.3
Clear colorless to pale yellow Liquid After Melting
0.9878 @ 20 DEG C/4 DEG C
21.35 °C
234 °C
195 °F
1.559-1.562
Practically insoluble in water;soluble in benzene, ethyl acetate, acetone, carbon disulfide.
2-8°C
1.33 hPa (63 °C)
LD50 orally in Rabbit: 2090 mg/kg LD50 dermal Rabbit > 5000 mg/kg
SPECIFIC OPTICAL ROTATION: +0.08 DEG
ANISE OIL ODOR
SWEET TASTE
Safety Information
NONH for all modes of transport
2
43-51/53
36/37-61
BZ9275000
Xi,N
Stable under normal temperatures and pressures.
P280
H317
trans-Anethole Use and Manufacturing
Separated by essential oil with high content of fennel brain (such as fennel oil). By the reaction of p-cresol and formaldehyde and then condensed with acetaldehyde.
platelet aggregation inhibitor
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