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trans-Anethole

trans-Anethole structure

trans-Anethole 

structure
  • CAS No:

    4180-23-8

  • Formula:

    C10H12O

  • Chemical Name:

    trans-Anethole

  • 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

  • Categories:

    Chemical Reagents  >  Organic Reagents

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].

trans-Anethole Basic Attributes

148.2

148.20

774229

224-052-0

29093090

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

Methods of 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.

Uses

platelet aggregation inhibitor

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