Ambros
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Ambros

Ambros est ingrediens in unguibus

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Ambrosius Basic Information

 

Product Name:

Ambros, Ambros

Synonyma:

1,5,5,9-Tetramethyl, XIII, oxatricyclo- [8.3.0.04,9] Tridecane
Amberlyn Super
Ambrobroxan
(-) - Ambroxide
Dodecahydrotetramethylnaphthofurran
PRAETERMITTO MMMCDLXXI
I -B] Furan, Dodecahydro, 3a, 6,6,9A, Tetrametyl- [3ar- (3a.Alpha., 5a.beta., 9a.Alpha., 9b.beta.
8.Alpha., XII, Oxido, 13,14,15,16, Tetranorlabdane
9BBeta 9BBTA)] - bet
Ambros
Naphthonis [2,1-B] Furan, Dodecahydro, 3a, 6,6,9A, Tetramethyl-, [3ar- (3a.a.a.a.
Naphthonis [2,1-B] Furan, Dodecahydro, 3a, 6,6,9A-Tetramethyl- [3atta- (3aalpha, 5a
n-epoxide
[3AR- (3aalpha, 5ABTA, 9aalpha, 9bbeta)] - Dodecahydro, 3a, 6,6,9A-Tetramethylnaphho [2,1-B] Furanum
Ambertoxan
Ambropur
(-) - XCIX + Ambroxide
Naphtho2,1-BFURRAN, Dodecahydro, 3a, 6,6,9A-Tetramethyl-, (3ar, 5s, 9s, 9br) -
(3ar, 5as, 9s, 9br):
Ambros

CAS:

6790-58-5

MF:

C16h28o

MW:

236.39

Einecs:

229-861-2

Product Categories:

 

Mol file:

6790-58-5.mol

 

Ambros proprietatibus

 

Point liquescens

74-76 ° C (Gen.)

alpha

-30 º (C = I% in Toluene)

PRAETERITUS 

273,9 ° C (praenuntiatum)

densitas 

0.939

vapor

0.066pa ad XXV ℃

Inlustro

3471

Storage temp.

Signatum in sicco, locus temperatus

forma

Pulveris ad Crystaline

colo

Alba ad paene alba

Odor

apud 1.00% in Tagropylene Glycol. Amberbris vetus charta dulcis labdanum sicco

Odor Type

electri

optical operatio

[Α] XX / XX XXIX °, C = I in Toluene

Aqua Solubility

1.88mg / l ad XX ℃

 

Ambrosius Synthesis


Descriptio

Ambrosius est synthetica spice cum peculiari odor naturalis Amberbris, et agnita est unum de optimis substituit naturalis Ambermegris. Est unus de maxime critica vestigium components naturalis Amberbris tincturam. Naturalis Amberbris est pretiosum animal spice. Est quaedam lapis in ventrem semen cete. Est vomitum vel excernitur in mare superficiem a cete et emittit specialis odore in aere diu.

Uses

Ambroxide potest esse:

Ut parare (+) - sclareolide per C? H? Oxidation belli.

Ut subiectum in C (SP3) -h alkylation / ARYlation studiis ex.

Ut subiectum in studiis ethereum hydrocarbon hydroperoxidation usura Singlet O2.

 

Applicatio

Ambroboxan habet fortis, proprium amberbris odor. In altum gradu unguibus et medicamine essentiam, quia non-vexo ad humanum corpus et non-allergic ad animalibus, idoneam ad odorem pro cutis, capillos et textilia. Saepe usus est in solaria, talcum pulveres, crepito et shampoos ad perfuming et fixing odor.

Definitio

Chobi: Diterpenenideus ex Sclareol, quod est reus in odorem amberbris (solidum, cerae, flammabiles substantia produci in digestivorum systema semen cete).

Praeparatio

Ambrosne naturaliter occurrit autoxidation vel photooxide in triterpenen secretus per semen cete.
Industrially, summus acacia acid paratus a Natolidol. Post acidum internum estterificatio, quod racemic Ambros erat adeptus.
Ambroxide est synthesized ex Sclareol, a component de essentiale oleum de Clary sapiens. Sclareol est oxidatively degradatus ad lactone, quod est hydrogenated ad correspondentes Diol. Et inde compositis dehydrated ad formare Ambroxide.

Synthesis

Periillyl Vocatus est usus ut rudis materia ad synthesize Nordrone Aether, quod oxidized per KMNO4 in Duo Steps (Helvetia Usus Ozone Oxidation, Russia utitur sodium chromate ozone). Id est (I) alkaline oxidatio; (II) infirmi acidum oxidatio. Et cadmiae adeptus est, tum cadmiae sarde, dehydrated et lactonized obtinere Ambrosolant.  Lactones reducuntur ad Ambroso cum Lithium aluminium hydride in aether (vel in borane in Tetrahydrofurran). D-Camphor-β-sulfonic acidum adhibetur ut cclclizing agente ad cyclize Diols obtinere Ambros (externis cyclizing agentibus includit sulphuric acidum, P, toluenesulfonic acidum et β-naphthallesulfonic acidum, etc). 

 

Praeparatio products et rudis materiae


Rudis materiae

Tetrahydrofurran -> para Toluene -> Ozone -> Naphthalene-II-Sulfonic Acidum -> Diborane -> D-Camphor -> Dihydro Alcohol

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