(1R)-(+)-α-Pinene CAS 7785-70-8 Puritas >98.0% (GC)
Elit ducens, princeps puritatis
(1R)-(+)-α-Pinene CAS 7785-70-8
(1S)-(-)-α-Pinene CAS 7785-26-4
Nomen chemicum | (1R)-(+)-α-Pinene |
Synonyma | (1R)-(+)-alpha-Pinene;(+) -α-Pinene;(+)-alpha-Pinene;D-(+)-alpha-Pinene;(1R,5R)-2,6,6-Trimethylbicyclo[3.1.1] hept-2-ene;(1R,5R)-2-Pinene |
CAS Number | 7785-70-8 |
CATTUS Number | RF-CC348 |
Stock Status | In Stock, Productio Capacity 3000MT/Anno |
Formulae hypotheticae | C10H16 |
M. Pondus | 136.24 |
Liquescens punctum | -62℃(lit.) @760 mmHg |
Mico punctum | 33℃ per Clausum-Cup |
Ferveret | 155.0~15.0℃(lit.) @760 mmHg |
Solubilitas in aqua | Insolubilis in aqua |
Solubilitas (Solubile in) | Aether, Chloroform, Alcohol |
Stipare Group | Ⅲ |
Brand | Ruifu Chemical |
Item | Specifications |
Aspectus | Hyalina liquida |
Puritas / Analysis Methodus | >98.0% (GC) |
Enantiometric Excessus | >97.0% |
Gravitas Imprimis (20/20℃) | 0.855~0.865 |
Index refractivus n20/D | 1.4640~1.4680 |
Imprimis Rotationes [a]20/D | +35.0° to +45.0° (Neat) |
Acidum Pendo | <0.50 mgKOH/g |
Aquae Caroli Fischer | <0.10% |
Non-Volatilis Materia Content | <1.00% |
Color per APHA | <30 |
Solubilitas, v/v 80% in Ethanol | 1, 16 .; |
Infrared Imaginis | Conformat ut Structure |
NMR | Conformat ut Structure |
Test Standard | Enterprise Standard |
GC Conditiones:
Columna Type: SE-54/BP-5
Columna Size: 50mx0.32mmx0.25um
Injector: 250℃
Detector: FID, 250℃
Solvendo: N/A
Oven Programma: 100℃ (2 min) ad 160℃ ad 4℃/min, 160℃ (2 min) ad 220℃ (5 min) ad 10℃/min
sarcina: Fluorinated Utrem, 44/53/58 ternas novas tympana ferrea galvanized, 145/175/190kgs rete per tympanum vel secundum exigentiam emptoris.
Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore
(1R)-(+)-α-Pinene (CAS: 7785-70-8) compositum est compositum ex terpeni genere, alterum e duobus isomers pineae.Alkenus est et quattuor membra reciprocus continet.(1R)-(+)-α-Pinene a gummi terebinthinae vel alio oleo essentiali in aplha piene pingui semotus est, multa in materia incipiendo ad summam synthesin terpineol, camphorae, dihydromyrcenoli, borneol, sandenoli et resinae terpennae adhibita est.(1R)-(+)-α-Pinene uti catalysts chiral.(1R)-(+)-α-Pinene adhibetur in praeparatione reagentium chiralium hydroborationis.(1R)-(+)-α-Pinene adhibetur in hydroboratione profectae et ketonum reductione.Adhiberi potest ut sapores et odores in oeconomiis cotidianis.(+) -α-Pinene compositio monoterpenoidis maxime in speciebus pini invenitur.Adhibentur ut medicamentatica, materiae chemicae et intermedia rudis, hoc productum est agens resolutionis optica et in aliis quoque agris adhiberi potest.Pinene sicut aroma modicum ad cotidianum saporem bergamot, folia lauri, casia, et citri, macis et aliorum saporis eduli.Praecipuus eius usus est post pyrolysin, myrcene, et synthesis geranioli, nerol, linalool, citronellol, citronellae, citrinalis, iononis et alia aromata gravissima.(1R)-(+)-α-Pinene anti-inflammatio est et in lato spectro antibiotico adhibetur.Inhibitorem acetylcholinesterase actionem exhibet, memoriam adiuvans.