(1S)-(-)-α-Pinene CAS 7785-26-4 Puritas >98.0% (GC)
Elit ducens, princeps puritatis
(1R)-(+)-α-Pinene CAS 7785-70-8
(1S)-(-)-α-Pinene CAS 7785-26-4
| Nomen chemicum | (1S)-(-)-α-Pinene |
| Synonyma | (-)-α-Pinene;(-)-alpha-Pinene;(1S)-(-)-alpha-Pinene;L-(-)-alpha-Pinene;(1S,5S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene;(1S,5S)-2-Pinene |
| CAS Number | 7785-26-4 |
| CATTUS Number | RF-CC349 |
| Stock Status | In Stock, Productio Capacity 3000MT/Anno |
| Formulae hypotheticae | C10H16 |
| M. Pondus | 136.24 |
| Liquescens punctum | -64℃ @760 mmHg |
| Ferveret | 155℃ @760 mmHg |
| Mico punctum | 33℃ per Clausum-Cup |
| Aqua Solubility | Insolubilis in aqua |
| Solubilitas (Solubile in) | Chloroform, Ethanol, Ether |
| Odor | Terebinthinum (Pine, acus, resina) Smell |
| Stipare Group | Ⅲ |
| Brand | Ruifu Chemical |
| Item | Specifications |
| Aspectus | Hyalina liquida |
| Puritas / Analysis Methodus | >98.0% (GC) |
| Gravitas Imprimis (20/20℃) | 0.856~0.861 |
| Index refractivus n20/D | 1.4640~1.4680 |
| Imprimis Rotationes [a]20/D | -35.0° ad -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;A luce et humore protege.
(1S)-(-)-a-Pinene (CAS: 7785-26-4) adhibetur in praeparatione ketonum hydroxyrii sicut hydroxycarvones.(1S)-(-)-a-Pinene monoterpene usus est in industriis ut odores, veneficiis, saporibus et fucis.Maior pars est olei pinei et olei terebinthinae.Isomerization ex α-pinene industriae compositas magnas sicut camphene, limonene et p-cymene reddit.(1R)-(+)-α-Pinene a gummi resinae terebenthinae segregatur.materia late usus est ad summam synthesim terpineol, camphorae, dihydromyrcenoli, borneol, sandenoli et resinae terpennae.(1S)-(-)-a-Pinene late in saporibus et odoribus adhibetur.(1S)-(-)--Pinene in oleis multarum specierum multarum arborum coniferarum reperitur, pineae notabiliter ac actionem insecticidam habet.(1S)-(-)-a-Pinene monoterpene est ac somnum ostendit augendi proprietatem per directam ligationem ad receptores GABAA-benzodiazepini (BZD) agendo modulatorem partialem in locum ligandi BZD.(1S)-(-)-a-Pinene est componentia resinae pineae et media synthetica chirali utilis est.
