depictio producti

Terpinen-4-ol Basic informationes

Overview Biological activities References

Product nomen:	Terpen-4-ol
Synonyma:	1-isopropyl-4-methyl-cyclohex-3-enol;1-methyl-4-isopropyl-1-cyclohexen-4-ol;1-methyl-4-isopropyl-1-cyclohexen-4-ol; (+/-) -4-HYDROXY-4-ISOPROPYL-1-METHYL-1-CYCLOHEXENE;
CAS;	562-74-3
MF:	C10H18O
MW:	154.25
EINECS:	209-235-5
Categoria:	Biochemistry; Terpenes, Terpenes (Alii); Monocyclica Monoterpenes, Intermedia & Fine Chemicals; Pharmaceuticals; Alphabetica Listings; C-DFlavors et Fragrances; Certified Naturalis Products;
Mol fasciculi:	562-74-3.mol

Terpinen-4-ol Chemical Properties

punctum liquescens	137-188 °C
alpha	+25.2°
fervens	212 °C
density	0.929
FEMA	2248 \| 4- CARVOMENTHENOL
refractivus index	n20/D 1.478
Fp	175 °F
repono temp.	-20°C
forma	Liquid
pka	14.94 ± 0.40 (Predicta)
Gravitas Imprimis	0.930.9265 (19℃)
color	Patet hyalina to subflavum
optical operatio	[α]20/D 27°, nivis
Aqua Solubility	Parum admodum solutum
JECFA Number	439
Merck	3935
Stabilitas:	Stabulum. Combustible. Agentibus oxidizing fortis repugnat.
InChIKey	WRYLYDPHFGVKC-UHFFFAOYSA-N
CAS Reference	562-74-3
NIST Chemia Reference	3-Cyclohexen-1-ol; 4-methyl-1-(1-methylethyl)-(562-74-3)
EPA Substantia Registry System	4-Terpineol (562-74-3)

Terpinen-4-ol Salutis Information

Terpinen-4-ol Usage

Chemical Properties	colore vel pallide flavo liquidum
Eventum	4-Carvomenthenol in oleo Cupressi macrocarpae relatum est lavender, Spanish origanum, Ledum palustre, Eucalyptus australiana var. A., Thuja occidentalis, l-forma inest oleo Eucalypti dives . et in quibusdam aliis essentiis ut Xanthoxylum rhetsa, una cum theca formam racemicam. Forma racemica invenitur in oleo camphorae. Nuntiavit in * pomum recens, apricota, succus aurantiorum, cortices olearum aurantiorum, citri, grapefruit; tangerina, anisum, cinnamomum, gingiber et muscata.
usus	Ostendit facilisis effectus. Antiseptic.
Definition	Chebi: A terpineol id est 1-menthenem hydroxytem sustinentem substituentem in positione 4 .
Gustus limina values	Sapor habet ad XXX ppm: dulce, citri viridi cum tropica fruity indolem.
Anticancer Research	Hoc etiam moleculae effectus per apoptoticum mechanism antitumor exhibet. Studia in muribus ferens a549 tumor xenografts (Quintans et al. 2013; Kiyan et al.2014).
Synthesis chemica	Unus ex pluribus terpinenol isomers, secundum positionem vinculi duplicis et entis the hydroxyl group, this terpen, cuius structura definita est Wallach, distillationibus fractis deprehendi potest. Est in natura ut dextro, levo et isomer racemico; synthetica productum est semper optically iners. The 1-terpineneol or 1-meththyl-4-isopropyl-3-cyclohexen-1-ol praeparatum a Wallach (Burdock, 1997).