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Grundinformationen
- Standard-SMILES
CC1=CCC(C(C)(C)O)CC1- InChIKey
WUOACPNHFRMFPN-UHFFFAOYSA-N- Summenformel
- C10H18O
- Durchschnittliche Molmasse
- 154,253 g/mol
- Monoisotopische Masse
- 154,1357652
Namen und Bezeichner
- Bevorzugter Name
- alpha-Terpineol
- IUPAC
- 2-(4-Methylcyclohex-3-en-1-yl)propan-2-ol
- Lokaler Name
- Terpineol
- Englischer Name
- Terpineol
- Summenformel
- C10H18O
- Molmasse
- 154.25
Namen und Synonyme
Datenbank-Bezeichner
- CAS
10482-56-1、8000-41-7、8006-39-1、98-55-5- PubChem CID
- 17100
- DTXSID
DTXSID5026625- ChEMBL
CHEMBL447597、CHEMBL449810、CHEMBL507795- ChEBI
CHEBI:22469- UNII
- 21334LVV8W
- EC Number
- 202-680-6、232-268-1、682-088-6、701-188-3
- Nikkaji
- J3.984E、J76.425F
Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 18 °C · 18°C
- Siedepunkt
- 213 · 213-218 °C (lit.)
- Dichte
- 0.934 g/mL · 0.934 g/mL at 20 °C (lit.)
- Dampfdruck
- 3 hPa · 3 hPa (20 °C)
- Brechungsindex
- 1.481 · 1.481-1.486
- Flammpunkt
- 95 °C · 95°C
- storage temp.
- 30 °C · Store below +30°C.
- Löslichkeit
- 1.25 ml/10ml, · ethanol: soluble1.25ml/10ml, clear to slightly hazy, colorless to light yellow (50% ethanol)
- Aggregatzustand
- Liquid
- Farbe
- Clear colorless to slightly yellow
- Geruch (Odor)
- 100 % · at 100.00 %. fresh clean woody pine floral lime
- Geruchsart
- herbal
- Biologische Quelle
- synthetic
- Wasserlöslichkeit
- slightly
- Dielectric constant
- 2.8 · 2.8(20℃)
- Stabilität
- Stable. Combustible. Incompatible with strong oxidizing agents, strong acids.
- Major Application
- cleaning productscosmeticsflavors and fragrancesfood and beveragespersonal care
- Kosmetik-Inhaltsstoffe Funktionen
- FRAGRANCEPERFUMING
- InChI
- 1S/2C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11;1-8(2)9-4-6-10(3,11)7-5-9/h4,9,11H,5-7H2,1-3H3;9,11H,1,4-7H2,2-3H3
- InChIKey
- WUOACPNHFRMFPN-UHFFFAOYSA-N
- SMILES
- CC(=C)C1CCC(C)(O)CC1.CC2=CCC(CC2)C(C)(C)O
- LogP
- 3.33 · 3.330 (est)
- CAS Datenbank
- 8000 · 8000-41-7(CAS DataBase Reference)
- EPA chemische Informationen
- Terpineol (8000-41-7)
Sicherheit und Regulatorisches
Sicherheitsdaten
- wgk
- 2
- tsca
- TSCA listed
- hs_code
- 29061990
- RTECS-Nr.
- WZ6600000
- risk_code
- 38-36/37/38-36/38-37/38
- Toxizität
- LD50 orally in Rabbit: 4300 mg/kg
- hazard_code
- Xi
- safety_code
- 37-36-26-24/25
- Speicherklasse
- 10 - Combustible liquids
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2
Chemie und Industrie
Anwendungen
BeschreibungTerpineol is a monoterpene alcohol that has been found in a variety of plants, including Cannabis, and has diverse biological activities. Terpineol contains the four isomers α-, β-, and γ-terpineol and terpinen-4-ol. α-Terpineol has antibacterial and antinociceptive properties. It is active against a variety of periodontopathic and cariogenic bacteria, including strains of P. gingivalis, F. nucleatum, and A. actinomycetemcomitans (MICs = 0.1-0.8 mg/ml), however, it is toxic to KB cells when used at a concentration of 0.8 mg/ml. It also reduces mechanical hyperalgesia, as well as spontaneous and palpation-induced nociception, in a mouse model of cancer-induced pain beginning on day 5 when administered at a dose of 50 mg/kg per day. Terpinen-4-ol has anticonvulsant properties, inhibiting pentylenetetrazol-induced seizures in mice when used at doses ranging from 50 to 200 mg/kg. α-Terpineol and terpinen-4-ol also have anti-inflammatory properties, reducing LPS-induced production of IL-1β, IL-6, and IL-10, but not TNF-α, in U937 cells. This product is a mixture of α-, β-, and γ-terpineol.
OccurrenceReported to be found in more than 200 derivatives from leaves, herbs and flowers [Fenaroli 's Handbook of Flavor Ingredients, 1971 ; Gildemeister & Hoffman, 1962).
VerwendenTerpineol is a monoterpene alcohol with potential antifungal, antioxidant and antiproliferative activities. This product is a mixture of isomers.
Darstellung
synthetischeFrom terpin hydrate by the splitting off of the elements of water by chemical means (Bedoukian, 1967).
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