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03900590

Terpinen-4-ol

primary reference standard

Synonym(e):

4-Carvomenthenol, 4-Terpinenol

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About This Item

Empirische Formel (Hill-System):
C10H18O
CAS-Nummer:
562-74-3
Molekulargewicht:
154.25
EG-Nummer:
209-235-5
MDL-Nummer:
MFCD00001562
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329747832
NACRES:
NA.24

Qualität

primary reference standard

Haltbarkeit

limited shelf life, expiry date on the label

Hersteller/Markenname

HWI

Lagerbedingungen

under inert gas

Brechungsindex

n20/D 1.478

bp

88-90 °C

Dichte

0.931 g/mL at 25

Anwendung(en)

food and beverages

Lagertemp.

−20°C

SMILES String

CC(C)C1(O)CCC(C)=CC1

InChI

1S/C10H18O/c1-8(2)10(11)6-4-9(3)5-7-10/h4,8,11H,5-7H2,1-3H3

InChIKey

WRYLYDPHFGVWKC-UHFFFAOYSA-N

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Allgemeine Beschreibung

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Anwendung

Reference Standard in the analysis of herbal medicinal products

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

174.2 °F - closed cup

Flammpunkt (°C)

79 °C - closed cup

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
HWI02540-2
HWI02540-1
HWI02540
HWI00630-3
HWI00630

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α-Terpinen analytical standard

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95652

α-Terpinen

Berberinchlorid Dihydrat phyproof® Reference Substance

PHL89487

Berberinchlorid Dihydrat

Terpineol mixture of isomers, 96%, FG

Sigma-Aldrich

W304506

Terpineol

α-Terpineol analytical standard

Supelco

30627

α-Terpineol

C Njume et al.
International journal of antimicrobial agents, 38(4), 319-324 (2011-07-15)
The aim of this study was to isolate and identify phytochemicals with anti-Helicobacter pylori activity from the stem bark of Sclerocarya birrea. The plant crude extract was fractionated by silica gel column and thin layer chromatography techniques, initially with ethyl
Mohsen I Afouna et al.
Journal of pharmaceutical sciences, 99(1), 119-127 (2009-06-17)
The objectives of the current study are (i) to maximize the ocular bioavailability of dorzolamide hydrochloride (DZD) through; (a) enhancement of the DZD corneal transport using various concentrations of selected natural terpene-4-ol enhancers, (b) increasing the contact time of the
Kotchaphan Chooluck et al.
Planta medica, 78(16), 1761-1766 (2012-10-03)
The purpose of this study was to investigate dermal pharmacokinetics of terpinen-4-ol in rats following topical administration of plai oil derived from the rhizomes of Zingiber cassumunar Roxb. Unbound terpinen-4-ol concentrations in dermal tissue were measured by microdialysis. The dermal
Yong Jie Li et al.
Environmental science & technology, 44(14), 5483-5489 (2010-06-17)
We investigated the condensed-phase reactions of biogenic VOCs with C double bond C bonds (limonene, C(10)H(16), and terpineol, C(10)H(18)O) catalyzed by sulfuric acid by both bulk solution (BS) experiments and gas-particle (GP) experiments using a flow cell reactor. Product analysis
R Loughlin et al.
Letters in applied microbiology, 46(4), 428-433 (2008-02-27)
The aim of this study was to compare both the antimicrobial activity of terpinen-4-ol and tea tree oil (TTO) against clinical skin isolates of meticillin-resistant Staphylococcus aureus (MRSA) and coagulase-negative staphylococci (CoNS) and their toxicity against human fibroblast cells. Antimicrobial
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