Ambrox
  • Ambrox Ambrox
  • Ambrox Ambrox
  • Ambrox Ambrox

Ambrox

Ambrox medicamentis in unguentis

Model:6790-58-5

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Ambrox Edition

 

Product nomen:

AmbroxAmbroxane

Synonyma:

1,5,5,9-TETRAMETHYL-13-OXATRICYCLO-[8.3.0.04,9] TRIDECANUM
AMBERLYN SUPER
AMBROXAN
(-) -AMBROXIDE
DODECAHYDROTETRAMETHYLNAPHTHOFURAN
FEMA 3471
1-b] furan, dodecahydro-3a,6,6,9a-tetramethyl-,[3aR-(3a.alpha.,5a.beta.,9a.alpha.,9b.beta.)]-Naphtho[2
8.alpha.-12-Oxido-13,14,15,16-tetranorlabdane
9aalpha,9bbeta)]-bet
Ambrox
Naphtho[2,1-b] furan, dodecahydro-3a,6,6,9a-tetramethyl-,[3aR-(3a.alpha.,5a.beta.,9a.al)
naphtho[2,1-b] furan, dodecahydro-3a,6,6,9a-tetramethyl-,[3atheta-(3aalpha,5a)
n-Epoxide
[3aR-(3aalpha,5abeta,9aalpha,9bbeta)]-dodecahydro-3a,6,6,9a-tetramethylnaphtho[2,1-b] furan
Amberoxan
Ambropur
(-)-AMBROXIDE 99+%
Naphtho2,1-bfuran, dodecahydro-3a,6,6,9a-tetramethyl-, (3aR,5aS,9aS,9bR)-
(3aR,5aS,9aS,9bR)-Dodecahydro-3a,6,6,9a-tetramethylnaphtho[2,1-b] furan
Ambroxane

CAS;

6790-58-5

MF:

C16H28O

MW:

236.39

EINECS:

229-861-2

Categoria:

 

Mol fasciculi:

6790-58-5.

 

Ambrox Chemica Properties 

 

punctum liquescens

74-76 °F (lit.).

alpha

-30 (c=1% in toluene)

fervens 

273.9±8.0 °C (Predicta)

density 

0.939

vapor pressura

0.016Pa at 25℃

FEMA

3471

repono temp.

Signatum in siccis, cella Temperature

forma

pulveris ad crystallinum

color

Alba ad fere alba

Odor

ad 1.00% in dipropylene glycol. ambergris vetus charta dulcis labdanum siccum

Odorem Type

electri

optical operatio

[α]20/D 29°, c = 1 in toluene

Aqua Solubility

1.88mg/L at 20℃

 

Ambrox Usus et Synthesis


Descriptio

Ambroxan est aroma syntheticum cum odore speciali ambergris naturalis, et agnoscitur unus ex primis substitutis ambergris naturalis. Est unum vestigium criticum maxime tincturae ambergris naturalis. Ambergris naturalis est aroma pretiosum animal. Est genus lapidis in ventre sperma ceti. Evomitur vel excernitur in aequore a ceto, singularem odorem in aere diu emittit.

usus

Ambroxide adhiberi potest;

Parare (+)-sclareolide per C?H?oxidationem belli.

Substratum in C(sp3)-H alkylation/arylation studiorum aetherum.

Subiecto in studio hydrocarbonae aetherei hydroperoxidationis utens singlet O2.

 

Applicationem

Ambroxan fortis, ambergris odoris proprium. Adhibetur in odoribus summus gradus et essentiarum medicamine, quia non irritat corpus humanum, et non allergicum animalibus, valde apta est odoribus pellibus, pilis et fabricis. Saepe usus est in soapibus, talci, crepitu et shampoos ad unguentandum et figendum odorem.

Definition

ChEBI: Diterpenoideum e sclareolo derivatum quod auctor est odoris ambergris (substantia solida, cerae, flammabilis in systemate spermatis ceti digestivorum producta).

Praeparatio

Ambroxene naturaliter occurrens autoxidationem vel photooxidum triterpenoidis a sperma cete secretae.
Industrie, Maximum acaciae acidum ex nerolidol praeparatum est. Post acidum interna aestimatio, Ambroxenum racemicum nactus est.
Ambroxide perstringitur e sclareolo, quod est elementum essentiale olei salvificae claritatis. Sclareol oxidative ad lactonam degradatur, quae hydrogenata est ad diol respondentem. Compositum inde dehydratum ad formam ambroxidam redactum est.

Synthesis

Vocatus Perillyl adhibetur ut materia rudis ad aetherem nordrone synthesinandam, quae duobus gradibus oxidatur a KMnO4 (Oxidatio ozona Helvetiae utitur, Russia oxidatio sodium chromatis utitur). Id est oxidatio alkaline; (2) oxidatio acidum debile. oxydatum obtinetur, dein oxydo madefacto, dehydrato et lacteo, ut ambroxolide obtinetur.  lactones reducuntur ad ambroxolum cum lithio aluminii hydride in aethere (vel borano in tetrahydrofuran). Acidum d-camphor-β-sulfonicum adhibetur ut agens cyclizans ad cyclizandas diolas ad obtinendum ambrocem (agentia aliena cyclising includunt acidum sulphuricum, acidum toluenesulfonicum et acidum β-naphthalenesulfonicum, etc.). 

 

Praeparatio Products et rudis materiae


Rudis materiae

Tetrahydrofuran-->PARA TOLUENE-->Ozone-->Naphthalene-2-acidi sulfonic-->Diborane-->D-CAMPHOR-->DIHYDRO CUMINYL ALCOHOL

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