86485

Terpinolen

technical, ≥85% (GC)

• Synonym(e): 4-Isopropyliden-1-methyl-cyclohexen, p-Menth-1,4(8)-dien, p-Meth-1-en-8-yl-formiat
• Empirische Formel (Hill-System): C₁₀H₁₆
• CAS-Nummer: 586-62-9
• Molekulargewicht: 136.23
• UNSPSC Code: 12352100
• NACRES: NA.22
• PubChem Substance ID: 329769467
• EC Number: 209-578-0
• Beilstein/REAXYS Number: 1851203
• MDL number: MFCD00049191
• Assay: ≥85% (GC)
• Form: liquid

Eigenschaften

• vapor density: ~4.7 (vs air)
• Quality Segment: 100
• vapor pressure: ~0.5 mmHg ( 20 °C)
• grade: technical
• assay: ≥85% (GC)
• form: liquid
• refractive index: n20/D 1.489 (lit.), n20/D 1.491
• bp: 184-185 °C (lit.)
• density: 0.861 g/mL at 25 °C (lit.)
• SMILES string: C\C(C)=C1/CCC(C)=CC1
• InChI: 1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4H,5-7H2,1-3H3
• InChI key: MOYAFQVGZZPNRA-UHFFFAOYSA-N

Beschreibung

General description

Terpinolene is a biogenically emitted monoterpene. Kinetics of gas phase reaction of OH and NO₃ radicals with terpinolene has been investigated. Biotransformation of terpinolene byAspergillus niger and several related species has been reported. Epoxidation of terpinolene in anhydrous conditions using alumina as a heterogeneous catalyst and hydrogen peroxide as the oxidant agent has been studied. It is an major component of essential oil extracted from the aerial parts of Clausena indica.[1]

Sicherheitshinweise

• pictograms: GHS08,GHS07,GHS09
• signalword: Danger
• hcodes: H304,H317,H410
• pcodes: P261 - P273 - P280 - P301 + P310 - P302 + P352 - P331
• Hazard Classifications: Aquatic Acute 1 - Aquatic Chronic 3 - Asp. Tox. 1 - Skin Sens. 1
• Lagerklasse: 3 - Flammable liquids
• flash_point_f: 141.8 °F - Seta closed cup
• flash_point_c: 61 °C - Seta closed cup
• ppe: Eyeshields, Gloves, type ABEK (EN14387) respirator filter