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29210

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Eucalyptol

analytical standard

Synonyme(s) :

1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane, 1,8-Cineole, 1,8-Epoxy-p-menthane

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About This Item

Formule empirique (notation de Hill):
C10H18O
Numéro CAS:
Poids moléculaire :
154.25
Numéro Beilstein :
105109
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Pureté

≥99.0% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.457 (lit.)
n20/D 1.458

Point d'ébullition

176-177 °C (lit.)

Pf

1-2 °C (lit.)

Densité

0.921 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

C[C@]12CC[C@H](CC1)C(C)(C)O2

InChI

1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3/t8-,10+

Clé InChI

WEEGYLXZBRQIMU-WAAGHKOSSA-N

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Description générale

Eucalyptol is a saturated monoterpene. It is a volatile oil with medicinal values naturally found in eucalyptus oil. It is a isoprenoid with 2-isoprene subunits (C10).

Application

Eucalyptol may be used as a reference standard for the determination of the analyte in:
  • Melon fruits by headspace solid-phase microextraction (HS-SPME) and gas chromatography-mass spectrometry.
  • Chrysanthemum flower by pressurized hot water extraction (PHWE) followed by headspace solid-phase microextraction (HS-SPME) and gas chromatography-mass spectrometry.
  • Pharmaceutical formulations by full evaporation technique extraction followed by capillary gas chromatography and ion-trap detection.
  • External analgesic pharmaceutical formulations by densitometric HPTLC analysis.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
It has been used as reference standard in densitometric HPTLC analysis for the determination of Eucalyptol from external analgesic pharmaceutical formulations.

Autres remarques

This compound is commonly found in plants of the genus: achillea angelica cinnamomum curcuma eucalyptus mentha salvia thymus valeriana zingiber

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Flam. Liq. 3 - Skin Sens. 1

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

125.6 °F - closed cup

Point d'éclair (°C)

52 °C - closed cup


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

Fast quantitative determination of aroma volatile constituents in melon fruits by headspace--solid-phase microextraction and gas chromatography-mass spectrometry.
Verzera A, et al.
Food Analytical Methods, 4(2), 141-149 (2011)
Volatile organic compounds determined in pharmaceutical products by full evaporation technique and capillary gas chromatography/ion-trap detection.
Schuberth, Jan
Analytical Chemistry, 68(8), 1317-1320 (1996)
Gas chromatography-mass spectrometry following pressurized hot water extraction and solid-phase microextraction for quantification of eucalyptol, camphor, and borneol in Chrysanthemum flowers.
Dong L, et al.
Journal of Separation Science, 30(1), 86-89 (2007)
Anti-inflammatory activity of 1.8-cineol (eucalyptol) in bronchial asthma: a double-blind placebo-controlled trial.
Juergens, U. R., et al.
Respiratory Medicine, 97.3, 250-256 (2003)
Sara Invitto et al.
Respiratory physiology & neurobiology, 259, 37-44 (2018-07-15)
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