Natural Methyl Eugenol
  • Natural Methyl EugenolNatural Methyl Eugenol

Natural Methyl Eugenol

Natural Methyl eugenol's cas code is 93-15-2

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Natural Methyl eugenol Basic information


Produktnavn:

Natural Methyl eugenol

CAS:

93-15-2

MF:

C11H14O2

MW:

178.23

EINECS:

202-223-0

Produkt kategorier:

INSEKTHORMON

Mol-fil:

93-15-2.mol



Natural Methyl eugenol Chemical Properties


Melting point 

−4 °C(lit.)

Boiling point 

254-255 °C(lit.)

density 

1.036 g/mL at 25 °C(lit.)

refractive index 

n20 / D 1.534 (lys)

Fp

>230 °F

storage temp. 

2-8 ° C

solubility 

0,5 g / l

Vannløselighet

uoppløselig

Merck

14,6073

BRN

1910871

Stability:

Stable. Combustible. Incompatible with strong oxidizing agents.

InChIKey

ZYEMGPIYFIJGTP-UHFFFAOYSA-N

CAS DataBase Reference

93-15-2 (CAS DataBase Reference)

NIST Chemistry Reference

Benzene, 1,2-dimethoxy-4-(2-propenyl)-(93-15-2)

EPA Substance Registry System

Methyleugenol (93-15-2)


Natural Methyl eugenol Safety Information


Hazard Codes 

Xn

Risikoverklæringer

22-36 / 37 / 38-40

Safety Statements 

26-36 / 37/39

WGK Germany 

1

RTECS 

CY2450000

HS kode

29093090

Data om farlige stoffer

93-15-2 (data om farlige stoffer)

Toksisitet

LD50 oralt hos rotter: 1560 mg / kg (Jenner)


Naturlig metyl eugenolbruk


Kjemiske egenskaper

colourless to light yellow liquid

Kjemiske egenskaper

Klar fargeløs topal gul væske. Krydret, jordaktig lukt. Bitter brennende smak. Dette kjemikaliet er brennbart.

Kjemiske egenskaper

Eugenol Methyl Ethe occurs in numerous essential oils, sometimes at a very high concentration. The ether is an almost colorless liquid with a mild-spicy, slightly herbal odor. It is prepared by methylation of eugenol and is used in perfumery (e.g., in carnation and lilac compositions) and in flavor compositions.

Kjemiske egenskaper

Eugenyl methyl ether has a delicate clove–carnation odor with a bitter, burning taste.

Hendelse

Rapportert i essensielle oljer av Myrtaceae og Luraceae; den ble opprinnelig identifisert i essensiell olje fra røttene til Asarum europaeum L og Asarum canadense LS Deretter ble den identifisert som hovedbestanddel av oljen fra Dacrydium franklinii Hook (97 5%), i Melaleuca bracteata F v M (blader, 90 til 95%), i Cinnamomum oliveri Bail (blader, 90 til 95%), og som en mindre bestanddel i oljer av betel, citronella, japansk calamus, pimenta, hyacinth, rose, basilikum, bukt, cajeput og andre. Rapportert funnet i oppvarmet blåbær, pepper, løvfrø, kjervel, sitronmelisse, alpinia-arter, nelliknøtter, muskatnøtt, pepper, myse, dragon, Ocimum sanctum, laurbær, myrteblad og bær, rosmarin, pimento bær og bladmasseolje

Uses

Duftingredienser i parfymer, toalettsaker og vaskemidler; smaksingrediens i bakevarer.

Air & Water Reactions

Uoppløselig i vann.

Reaktivitetsprofil

Methyl eugenol is incompatible with strong oxidizers . May react exothermically with reducing agents to release hydrogen gas.

Fare

Mulig kreftfremkallende.

Fire Hazard

Methyl eugenol is combustible.

Sikkerhetsprofil

Confirmed carcinogen. Poison by intravenous route. Moderately toxic by ingestion and intraperitoneal routes. A skin irritant. Mutation data reported. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. Some other alkenylbenzenes have carcinogenic activity. See also EUGENOL, ALLYL COMPOUNDS, and ETHERS



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