5-Pentylresorcin

Bezeichnung:5-Pentylresorcin

CAS-Nr500-66-3

Englisch Name:Olivetol

CBNumberCB3204779

SummenformelC11H16O2

Molgewicht180.24

MOL-Datei500-66-3.mol

Synonyma

5-Pentylresorcin

5-Pentylresorcin physikalisch-chemischer Eigenschaften

Schmelzpunkt	46-48 °C(lit.)
Siedepunkt	164 °C
Dichte	1.068±0.06 g/cm3(Predicted)
Flammpunkt	>230 °F
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
Löslichkeit	Chloroform (Slightly), Methanol (Slightly)
Aggregatzustand	Solid
pka	9.59±0.10(Predicted)
Farbe	Colourless to Beige
Stabilität	Light Sensitive
InChI	InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3
InChIKey	IRMPFYJSHJGOPE-UHFFFAOYSA-N
SMILES	C1(O)=CC(CCCCC)=CC(O)=C1
CAS Datenbank	500-66-3(CAS DataBase Reference)
NIST chemische Informationen	1,3-Benzenediol, 5-pentyl-(500-66-3)
EPA chemische Informationen	Olivetol (500-66-3)

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38
S-Sätze:	26-36/39
WGK Germany	3
RTECS-Nr.	VH2880000
HS Code	2907290090

Gefahreninformationscode (GHS)

Olivetol Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/39:Bei der Arbeit geeignete Schutzkleidung und Schutzbrille/Gesichtsschutz tragen.
Chemische Eigenschaften
Olivetol is an off-white crystals or olive to light purple waxy solid. Forms monohydrate (melting point: 102-106°F). Olivetol is a member of the class of resorcinols that is resorcinol in which the hydrogen at position 5 is replaced by a pentyl group. It has a role as a lichen metabolite.
Physikalische Eigenschaften
light purple to brown crystalline mass.
Application
Olivetol is a precursor in various syntheses of tetrahydrocannabinol.
Verwenden
Olivetol was used as a template molecule in the synthesis of molecularly imprinted polymer (MIP). It was also used as an inhibitor of (S)-mephenytoin 4'-hydroxylase activity of recombinant CYP2C19.
Definition
ChEBI: Olivetol is a member of the class of resorcinols that is resorcinol in which the hydrogen at position 5 is replaced by a pentyl group. It has a role as a lichen metabolite.
synthetische
olivetol can also be formed through hydrolysis of intermediate polyketide CoAs or spontaneous cyclization.
Synthesis Reference(s)
The Journal of Organic Chemistry, 42, p. 3456, 1977 DOI: 10.1021/jo00441a036
Allgemeine Beschreibung
Olivetol appears as off-white crystals or olive to light purple waxy solid. Forms monohydrate (melting point: 102-106°F). (NTP, 1992)
Air & Water Reaktionen
Sensitive to air. Insoluble in water.
Reaktivität anzeigen
Olivetol is incompatible with acid chlorides, acid anhydrides and oxidizing agents.
Brandgefahr
Olivetol is probably combustible.
Biologische Aktivität
Olivetol (5-Pentylresorcinol, 5-n-Amylresorcinol) is a naturally occurring organic compound being a precursor in various syntheses of tetrahydrocannabinol. It acts as a competitive inhibitor of the cannabinoid receptors CB1 and CB2.
Sicherheit(Safety)
Olivetol is still a very new product. It has not been researched nearly enough to prove it's safe to use. So far, no one has reported any adverse side effects as far as we know. Until more information is available, carefully control your THC intake instead of relying on an untested gelcap.
Mode of action
When you look at olivetol's molecular structure, it'll look very familiar. It's as if someone took a THC molecule and sliced it in two. Olivetol, like THC, works by binding with the CB1 receptors that exist all over your body and brain. But, olivetol is thought to be smaller and stickier than THC, so that helps it reduce a raging high in two ways. First, it slips into any open receptors before THC can get there to block them—so you won't get any higher. Second, it bumps into THC molecules that are already lodged in a CB1 receptor to knock them loose and take their place. That's how it brings you down.
According to numerous personal accounts, olivetol works, but we don't know exactly how it does so. More research and investigation is needed, but in theory it's very similar to how Narcan acts to reverse opiate overdoses.

Olivetol Upstream-Materialien And Downstream Produkte

5-Pentylresorcin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

500-66-3, Olivetol Verwandte Suche:

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