ethyl Cinnamate
  • ethyl Cinnamateethyl Cinnamate

ethyl Cinnamate

Ethyl cinnamate 's Code est cas 103-36-6

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Ethyl cinnamate Basic notitia


Application aromata multa nimis et odor Insecta Content analysis usus ut ELOGIUM quantum ad terminum licita maxima, et residuum maximum licita chemicae Lorem modum adhiberi solet:


Product Name:

ethyl cinnamate

CAS:

103-36-6

MF:

C11H12O2

MW:

176.21

EINECS:

203-104-6

Mol File:

103-36-6.mol



Donec ethyl cinnamate Properties


Liquescens punctum

6-8 ° C (Litt.)

Ferveret

CCLXXI ° C (Litt.)

density

1.049 g / ml at20 ° C (Litt.)

potenti

MMCDXXX | ETHYL CINNAMATE

refractivam index

n20 / D 1.558 (lit.)

Fp

> CCXXX ° F

temp repono.

Armarium frigidarium (IV + ° C)

forma

Liquid

color

Patet sine colore flavo topale

aqua Solubility

posse dissolvi

Merck Poland

14,2299

Number JECFA

659

BRN

1238804

Stabilitatem:

Firmum. repugnantes oxidizing magnis agentibus acidis bases deiciatur agentium. Combustibilis ab aere obscuritas.

CAS DataBase Reference

103-36-6 (CAS DataBase Reference)

Quaestiones NIST Reference

trans-Ethyl cinnamate (103-36-6)

Ratio Subcriptio quod substantia EPA

Ethylcinnamate (103-36-6)


Safety ethyl cinnamate Information


risk Denunciationes

20-22

Denunciationes salutem

23-24 / XXV

Germania WGK

1

RTECS

GD9010000

Capparis

Ita

HS Code

29163990


Synthesis ethyl cinnamate Et Usu


chemicae

Videtur quod prope hyalina, perspicuus liquor pinguis luce diuturna cinnama et mel dulcis fragum in odorem suavitatis. Quod cum actio non habet optical liquescens punctum XII  ° C, in punctum CCLXXII  ° C ferventis punctum et mico  ° C. 93.5 Est miscible in ethanol praeservatum, aetheria vel maxime non-volatile olea. Est glycerolum fere dissolvi in ​​aqua. Est solutum in ignominiam propylene glycol.
Fontes iuris Germanici antiqui in sua natura existit product balsama et oleum galangal est.

modum productio

Potest esse quod obtainedthrough esterification inter ácido et in ethanol praeservatum a cede presenceof SULPHURATUS acidum ad de LX%. Potest etiam esse reactionem derived throughthe bewteen benzaldehyde et ethyl acetate.
Potest obtinetur per reactionem, et inter benzaldehyde ethylacetate coram sodium metallum.
Factum est ex incalescentia ex ácido, in ethanol et acidum SULPHURATUS C Â ° C ad conspectu aluminium sulfate.

Description

Esther isthe de ethyl cinnamate ácido et ethanol. Non est praesens in essential ofcinnamon oleum. Pura est ethyl cinnamate 'fruity balsamica et incensum odoris suavissimi simile electro cinnamomum cum nota ".
Et inde est relatus yl p-mono Amine oxidase esse inhibitor.

Properties eget

Cinnamate est ethyl mel dulcis, et nota odor balsami.

Properties eget

sine colore humor

usibus

Pigmentaria, CONDITIO posui.

productio modos

Cinnamate est ethyl styracis in oleo Kaempferia auriculiformis aliique complures exequitur. Est per productum cum recta esterification esterification in ethanol praeservatum Cinámico Acidum azeotropic condiciones sub-genus Claisen per condensationem vel ethyl et acetate benzaldeyde coram sodium metallum.

Praeparatio

Acidum Ccinnamic ° C ut calefiat; alcohole SULPHURATUS acidum coram aluminium sulfate, et Claisen in con [I] est in auge, benzaldehydeand ethyl acetate

Aroma limine values

DEPREHENSIO: XVII ut 40ppb

Saporem limine values

Ppm Tastecharacteristics ad XX: balsamica, pulverulosum, fruity, baca, ferrum et amomum et dulce et viridi.


Rudis materia et Products ethyl cinnamate Praeparatio


et rudis materiae

Sodium -> aluminium sulfate -> trans-ácido -> Vocatus acidum Hydrochloric

Praeparatio Products

Ozagrel -> I-III-Phenyl, propanol -> Ethyl III-phenylpropionate

S CAS nulla est ethyl cinnamateâ 103-36-6.

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