Alpha-Pinene

Product Name:

Alpha-Pinene

Synonym:

Î ± -Pinene 80-56-8 (±) ene -pin-II,;, Trimethyl-6,6-bicyclo [3.1.1] Heptateucum, II-ene: 2,6,6, trimethylbicyclo- (III, 1,1) -2-heptene: 2,6,6, Trimethylbicyclo (3.1.1) -2-II-Heptateucum, ene: 2,6,6, Trimethylbicyclo (3.1.1) -2-heptene:-pin II -ene: Terpenehydrocarbon

CAS:

80-56-8

MF:

C10H16

MW:

136.23

EINECS:

201-291-9

Product Categories:

Alkenes Cyclic: Organic Building Blocks

Mol File:

80-56-8.mol

Liquescens punctum

-55 ° C

Ferveret

155-156 ° C (Litt.)

density

0.858 g / ml at25 ° C (Litt.)

potenti

MMCMII | Alpha-PINENE

refractivam index

n20 / D 1.465 (lit.)

Fp

XC ° F

temp repono.

regio Flammables

forma

Liquid

color

patet hyalinae

Odor Limen

0.018ppm

aqua Solubility

posse dissolvi

Merck Poland

13,7527

Number JECFA

1329

Stabilitatem:

Firmum. Flammable.Incompatible magnis oxidizing agentium.

CAS DataBase Reference

80-56-8 (CAS DataBase Reference)

Quaestiones NIST Reference

«Alpha» -Pinene (80-56-8)

Ratio Subcriptio quod substantia EPA

.alpha., Pinene (80-56-8)

aleam Codes

XI, N, X, M

risk Denunciationes

10-36 / XXXVII / 38-43-50-65-51 / 53-38-36 / 38-20

Denunciationes salutem

26-36 / 37-61-37 / 39-29-16-36 / XXXVII / 39.7 / 9-62

RIDADR

III IR MMCCCLXVIII / PG III

Germania WGK

1

RTECS

DT7000000

Autoignition Temperature

CDXCI ° F

HazardClass

3.2

PackingGroup

III

HS Code

29021990

Ancipitia substantiae Data

80-56-8 (Malo Periculosam substantias Indicium)

Properties eget

fluidi odor aturpentine

Properties eget

Î ± -Pinene est mostwidespread pinene isomer. (+) - Î ± -Pinene (1R, 5R) -2,6,6, trimethylbicyclo [3.3.1] Heptateucum, II-ene, occurs: exempli gratia, oilfrom Pinus palustris L. in., Usque ad eiusdem collationem LXV%; Pinus caribaea quae de American oleum et Soland Pinuspinaster oleum de LXX%, et 70a LXXX%, respective, ex laevorotatory isomer, (?) - Î ± -Pinene (1S, 5S) -2,6,6, trimethylbicyclo [ 3.3.1] Heptateucum, II-enc.
Î ± -Pinene patitur multis reactiones, haec sunt quorum usus est in industriam thefragrance super hydrogenation, Î ± -pinene convertitur ad pinane, qui facti sunt magni momenti materia in carcere industria industriae processesused in odorem et saporem. -Pinene Î ± possunt, isomerized toβ pinene magna selectivity ad eos dictos isto, pinene formation. Withsimultaneous cedit hydratationis circulum ostium terpineol et Cis-hydrate terpin. Pyrolysisof Î ± -pinene cedit mixtisque ocimene et alloocimene.
Pura Î ± -pinene adeptus est per destillationem oleo terebinthinae sesquili. Ut fragrancesubstance, ut solebat amplio odorem notitiæ products.However industriae, CH Boheman farmore momenti incipiens quasi materia fidei syntheses in odio, forexample, terpineols, borneol et caphura.

Properties eget

Î ± -Pinene habet acharacteristic odorem notitiæ abiete. Est sicut resinae terebenthinae. Oxidized in materia, sicut resinae hasa odoris suavissimi componendum.

usibus

Î ± -Pinene asstandard usus est in solidum, Headspace tempus microextraction-volatile Gas chromatographicanalysis ex olea I oliva virgo in suis Revolutionibus componit. Hoc erat in cesium thesynthesis est potentiale, habens medicare serentis heteropolyacid applicationem inbiodiesel synthesis.

usibus

Î ± -Pinene asstandard usus est in solidum, Headspace tempus microextraction-volatile Gas chromatographicanalysis ex olea oliva virgo in suis Revolutionibus componit. Hoc erat in cesium thesynthesis est potentiale, habens medicare serentis heteropolyacid applicationem inbiodiesel synthesim

definitio

ChEBI: pinene thatis bicyclo A [3.1.1] Heptateucum, II-II ene competit substituendi sibi yl coetus ad positions, respectively 6 VI.

productio modos

Î ± -Pinene occursnaturally in varietate arborum et fruticum, comprehendo plus quam CD essentialoils et aerem prope silvas coniferas concentratione potest pervenire 500â MCC mg / US m3.Total coniferi et deciduis siluas inde egreditur -pinene Î ± 6.6 amountsto annuatim decies centena millia talentorum. Aestimatum Belgarum emissionem rate of -pinene fromnatural fontes Î ± 1,84 in atmosphaera sit × X -10 g / cm3 / s.

Praeparatio

Ex pistacias terebinthi bydistillation.

Aroma limine values

DEPREHENSIO: 2.5 62ppb. Notas odor 1.0% terpy citri et aromatici silvestris pinus andturpentinelike camphoraceous nutmeglike simpliciter tenui frigore et tropicae fructus et elevabis freshherbal contentione revocabit.

Saporem limine values

Ppm Tastecharacteristics ad X: insaniam inciderunt silvestri, resinae terebenthinae Piney et terpy cum camphoraceousand notas. Herbal non habet, CONDITUS leviter tropicae mango atque extenuatis proponuntur.

Communia

A patet et terebinthum colorlessliquid odoris suavissimi componendum. XCI mico punctum F. Andinsoluble aqua rarior aqua. Vapores omnia graviora sunt caeli. Utendum est, qui menstrui.

Agrippina Minor aqua Aeris &

Flammable.Insoluble altus aqua.

Reactividad Profile

intentius agentibus oxidizing mayreact Pinene alpha magnis. Sit agere exothermically withreducing agentibus dimittere gaseous hydrogenii.

salutem DISCRIMEN

Nocivis ifswallowed accepi, aut absorbetur per cute. Summa concentratione alto areextremely exitio mucosae respirandi tractu eyesand cutem. Symptomata potest includere nulla ardenti sentiendi vim continuae tussis, wheezing, LARYNGITIS habent, brevitatem spiritus, capitis, nausea et vomitus.

ignis DISCRIMEN

Britannica specialis ofCombustion Products: Vapor ut longius iter ad fontem et ofignition flashback. Strepitus fiat per ignem mixtione aeris continentis conditions.Forms perurbane.

Contact allergens

Alpha-pinene themajor non sane pars terebenthinae (circiter LXXX%). Non existit in forma levogyre inEuropean resinae terebinthinae sesquili inventi sunt in specie et in dextrogyre inNorth-Americae. Sensitisation spirituum maxime fit in cupio pictorem, politores, andvarnishers et qui in unguentum et in ceramics industria.

salutem Profile

A byinhalation venenum mortiferum. Et mediocri toxicus per ingestion. An oculus, tunicae mucosae, cutis irritationem andsevere hominum. Flammabiles liquidum sit. A ignis aleam periculo whenexposed calore, flammae aut oxidizing materiae. Pugnare ignis uti spuma Co2 sicco eget. Uacuatur in contactum cum nitrosyl perchlorate.

Praeparatio Products

Camphene -> Dihydromyrcenol -> (1S) - (-) - alpha Pinene

et rudis materiae

terebinthinae oleum