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Estragole

Estragole structure

Estragole 

structure
  • CAS No:

    140-67-0

  • Formula:

    C10H12O

  • Chemical Name:

    Estragole

  • Synonyms:

    Benzene,1-methoxy-4-(2-propen-1-yl)-;Anisole,p-allyl-;Estragole;Benzene,1-methoxy-4-(2-propenyl)-;Ether,p-allylphenyl methyl;1-Methoxy-4-(2-propen-1-yl)benzene;p-Allylanisole;Chavicol methyl ether;Esdragol;Esdragon;Isoanethole;p-Methoxyallylbenzene;Methyl chavicol;Chavicol,O-methyl-;Esdragole;4-Methoxyallylbenzene;4-Allylanisole;3-(p-Methoxyphenyl)propene;Estragol;4-Allylmethoxybenzene;1-Allyl-4-methoxybenzene;Chavicol,methyl-;1-Methoxy-4-(2-propenyl)benzene;p-Allylphenyl methyl ether;3-(p-Methoxyphenyl)-1-propene;3-(4-Methoxyphenyl)-1-propene;NSC 404113;O-Methylchavicol;Estragenole;AUSTL 21320;Esteragol;3-(4-Methoxyphenyl)propene;1407-27-8;77525-18-9

  • Categories:

    Cosmetic Ingredient  >  Perfuming

Description

Estragole (4-Allylanisole), a relatively nontoxic volatile terpenoid ether, is a major component of the essential oil of many plants. Estragole has potent local anesthetic activity and dose-dependently blocks nerve excitability[1]. Estragole displays anti-toxoplasma activity[2].

Estragole Basic Attributes

148.2

148.20

1099454

205-427-8

2909309090

Characteristics

9.2

3.4

Clear colorless Liquid

0.9645 g/cm3 @ Temp: 21 °C

28-35 °C

215.5 °C

178 °F

1.505

0.178 mg/mL at 25 °C

Store below +30°C.

0.165 mm Hg at 25 °C (est)

Oral-rat LDL0: 1230 mg/kg; Oral-Mouse LD50: 1030 mg/kg

Flammable; burning produces irritating fumes

Odor reminiscent of anise with a corresponding sweet taste (differing from anethole)

Sweet taste reminiscent of anise (differing from anethole)

Safety Information

NA 1993 / PGIII

3

22-38-43-68-40

26-36/37

BZ8225000

Xn

Treasury is ventilated, low temperature and dry; stored separately from food materials

Stable. Flammable. Incompatible with strong oxidizing agents.

P280

H302-H317-H341-H351

Toxicity

moderately toxic

Estragole Use and Manufacturing

Methods of Manufacturing

From turpentine or tarragon oil fractionation. From the reaction of allyl bromide and magnesium methoxyphenol.

Uses

In perfumes and as flavor in foods and liqueurs.

Computed Properties

Molecular Weight:148.20
XLogP3:3.4
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:148.088815002
Monoisotopic Mass:148.088815002
Topological Polar Surface Area:9.2
Heavy Atom Count:11
Complexity:112
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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