|
Product Name: |
IV-of-Terpinen |
|
Synonym: |
I, isopropyl-IV-yl cyclohex-III-enolum explorabantur, I-Methyl-IV-isopropyl-I-cyclohexen-IV-Español, I-yl IV, isopropyl-I-cyclohexen-IV-o (IV-terpineol) , I-IV-of-para-Menthen (+/-) --hydroxy-IV-I-IV-isopropyl mETHYL-I-CYCLOHEXENE: CARVOMENTHENOL-IV: I-IV-TERPINEN, Domine (+/-) -III-IV-METHYL -1, isopropyl CYCLOHEXEN I, Domine, |
|
CAS: |
562-74-3 |
|
MF: |
C10H18O |
|
MW: |
154.25 |
|
EINECS: |
209-235-5 |
|
Product Categories: |
Biochemistry: Terpenes: Terpenes (Alii); Monocyclic Monoterpenes; & denique chemicals Intermediates, Pharma: Alphabetical Listings; C-DFlavors et Fragrances: Naturalis Certified Products: et Sapor Fragrances, C, D |
|
Mol File: |
562-74-3.mol |
|
|
|
|
Liquescens punctum |
137-188 ° F |
|
delta |
25.2 ° + |
|
Ferveret |
CCXII ° F |
|
density |
0.929 |
|
potenti |
MMCCXLVIII | IV-CARVOMENTHENOL |
|
refractivam index |
n20 / D 1,478 |
|
Fp |
CLXXV ° F |
|
temp repono. |
-20 ° C |
|
forma |
Liquid |
|
pka |
14.94 ± 0,40 (Praedicta) |
|
Gravitas specifica |
0.930.9265 (19a) |
|
color |
Patet hyalina flavo toslightly |
|
optical actio |
[Î ±] XX / D XXVII °, ita concinnum |
|
aqua Solubility |
ipsum slightlysoluble |
|
Number JECFA |
439 |
|
Merck Poland |
3935 |
|
Stabilitatem: |
Firmum. Combustible.Incompatible magnis oxidizing agentium. |
|
InChIKey |
WRYLYDPHFGVWKC UHFFFAOYSA-N, |
|
CAS DataBase Reference |
562-74-3 (CAS DataBase Reference) |
|
Quaestiones NIST Reference |
Cyclohexen-of-I-III, IV, yl 1- (I-methylethyl) - (562-74-3) |
|
Ratio Subcriptio quod substantia EPA |
Terpineol-IV (562-74-3) |
|
aleam Codes |
xII |
|
risk Denunciationes |
22-36 / XXXVII / XXXVIII |
|
Denunciationes salutem |
26-36-37 / XXXIX |
|
Germania WGK |
2 |
|
RTECS |
OT0175110 |
|
HS Code |
29061990 |
|
Properties eget |
paleyellow hyalinae vel murram |
|
res |
Carvomenthenol-IV (dextro) relata nunc ad oleum de macrocarpalavender Cupressus macrocarpa, Spanish origanum, Ledum palustre, Eucalyptus Australiana var. A., Pinus nigra, etc.-l et est praesens in specie per aliquam divesand eucalyptus oleum ab aliis essentiis ut Xanthoxylum rhetsa, theracemic simul cum forma. Quod est forma in racemic caphura oleum. Nuntiavit infresh inveni malum, apricots, aurantiaco sucus, oleis et aurantiacis cortices, CITRUM, grapefruit, tangerines, anethum, cinnamomum, gingiberi et nutmeg. |
|
usibus |
Antioxidanteffects ostendit. ANTISEPTICA REMEDIA. |
|
definitio |
ChEBI: A est terpineolthat I-hydroxy menthene portantes in lecto positus in IV substituent. |
|
Saporem limine values |
Tastecharacteristics ad XXX ppm, suavis, citri et viridi pars tropicale fruitycharacter. |
|
Research anticancer |
Etiam hic per effectus moleculeexhibits antitumor apoptotic mechanism. Studies in weredone micebearing A549 tumore Xenophon (Quintans et al. MMXIII: et Kiyan al.2014). |
|
Synthesis eget |
Una severalterpinenol isomers, fretus loco per eumdem ex duplici et hydroxyl foedere coetus, hoc terpene, cuius structuram defined byWallach esse, potest inveniri separatim ab fractus distillation. Quod existit in natura asthe dextro, et levo racemic isomer; synthetica alwaysoptically productum est absque actu. I-de-IV-meththyl terpineneol or1, isopropyl-of-I-III-cyclohexen parata est ab Wallach (Burdock, MCMXCVII). |
