Sin Cinnamyl

Product Name:

Vocatus Cinnamyl

Synonym:

(E) phenyl-II-3-I-of-propen (2E) Phenyl-II-3-I-of-propen: Phenyl-I-I-III-of-propen: Propen-II-1- of, phenyl-, III, II-III-Fenyl propen-I-of-, phenyl-II-III-I-o-propen: phenyl-II-III-propenol: en-I-II-III-phenyl huius, -ol

CAS:

104-54-1

MF:

C9H10O

MW:

134.18

EINECS:

203-212-3

Product Categories:

eget reagens; pharmaceutical medium, phytochemical; referat signa Chinesemedicinal ex herbis (TCM) .; herbal standardized extract: stibio: Pharmaceutical intermedia, Benzhydrols Benzyl & SpecialAlcohols

Mol File:

104-54-1.mol

Liquescens punctum

30-33 ° C (Litt.)

Ferveret

CCL ° C (Litt.)

density

1.044 g / ml at25 ° C (Litt.)

vapor densitatem,

4.6 (VS caeli)

vapor pressura

<0.01 mm Aggaei (XXV ° C)

potenti

MMCCXCIV | CINNAMYL ALCOHOL

refractivam index

1.5819

Fp

> CCXXX ° F

temp repono.

2-8 ° F

solubility

H2O Prunus: solutum;

forma

Minimum Fused MeltingCrystalline Solidum

Gravitas specifica

1.044

color

album

aqua Solubility

1.8 g / L (XX ºC)

Number JECFA

647

Merck Poland

14,2302

BRN

1903999

Stabilitatem:

Firmum. Fortis Incompatiblewith oxidizing agentium.

InChIKey

OOCCDEMITAIZTP QPJJXVBHSA-N,

CAS DataBase Reference

104-54-1 (CAS DataBase Reference)

Quaestiones NIST Reference

I-II-of-Propen, phenyl--III (104-54-1)

Ratio Subcriptio quod substantia EPA

Phenyl-III-II-I-of-propen (104-54-1)

aleam Codes

xII

risk Denunciationes

22-36 / 38-43-36

Denunciationes salutem

26-36 / 37-37 / 39-24-24 / XXV

RIDADR

2811

Germania WGK

2

RTECS

GE2200000

F

10-23

Capparis

Ita

HS Code

29062990

Ancipitia substantiae Data

104-54-1 (Malo Periculosam substantias Indicium)

Aedes

LD50 (g / kg): apud 2.0orally redibant, > 5.0 dermally cuniculosae Celtiberiae (Letizia)

usibus

Spiritus enim ejus, et pigmentaria Cinnamyl isvaluable in fixative proprietatibus. Est componentof plures flos taceam (lilac, hyacinthino pallio, et lilium convallium) et isa est materia incipiens cinnamyl esters, quarum aliquot valuablefragrance materiae. Flavor in compositions, quia Vocatus est usum fructum off odorem cinnamonnotes et elegis.

Praeparatio

Vocatus Cinnamyl isprepared in scale per reductionem cinnamaldehyde cīvitās industrialis est. Methodsare tribus praecipue utile:
I) in Meerweinâ Ponndorf reductionem, non reducitur in cinnamaldehyde cinnamicalcohol (tradite de LXXXV%) de isopropyl alcohol aut benzyl coram eumdem aluminium alcoholate correspondentes.
II) A XCV% of tradite Cinnamyl ipsum adeptus est per electionem selectivam hydrogenation eumdem carbonyl cinnamaldehydewith in coetus, exempli gratia, an osmiumâ carboncatalyst.
III) High Cinnamyl Vocatus cedit haberi potest nisi per reductionem ad alcali ofcinnamaldehyde borohydrides. Formatio dihydrocinnamic alcoholis vitatur.

Properties eget

Vocatus est Cinnamyl amoenam, floris odor et amaritudine infestatur.

usibus

Vocatus est cinnamyl cinnamomum naturalis originem in cortice signant, ut possit etiam synthetically factorum. In stibio est usus ut a CONDITIO agent.In odore, pigmentaria, quasi deodorant in solution in glycerolum 12,5%.

Aroma limine values

DEPREHENSIO: I: ppm, Cis- speciem LXXXI bilionem; trans- forma, 2.8: ppm

Saporem limine values

Tastecharacteristics ad XX ppm, viridis, floral, CONDITUS et mel et fermentedyeasty simpliciter.

Synthesis eget

Impetrata ab styracis originallyby saponificationem extractionis; synthetically, vel kalium sodium hydroxide inducendo quasi ad ofcinnamaldehyde.

Ratio purificatione

Crystallize thealcohol diethyl ex aetheris oris / pentane. [VI Beilstein ego 281.]