Terpinolene ≥95%, FG

Sinônimo(s):

4-Isopropylidene-1-methylcyclohexene, p-Menth-1,4(8)-diene, p-Meth-1-en-8-yl-formate

Sobre este item

Fórmula empírica (Notação de Hill):

C₁₀H₁₆

Número CAS:

586-62-9

Peso molecular:

136.23

FEMA Number:

3046

Council of Europe no.:

2115

UNSPSC Code:

12164502

PubChem Substance ID:

24901446

Flavis number:

1.005

EC Number:

209-578-0

NACRES:

NA.21

MDL number:

MFCD00049191

Beilstein/REAXYS Number:

1851203

Organoleptic:

fresh; woody; citrus; pine; sweet

Grade:

FG, Halal, Kosher

Biological source:

synthetic

Food allergen:

no known allergens

biological source

synthetic

Quality Segment

400, 300

grade

FG, Halal, Kosher

reg. compliance

EU 1334/2008 & 872/2012

vapor density

~4.7 (vs air)

vapor pressure

~0.5 mmHg ( 20 °C)

assay

≥95%

refractive index

n20/D 1.489 (lit.)

bp

184-185 °C (lit.)

density

0.861 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

fresh; woody; citrus; pine; sweet

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

General description

Terpinolene is a volatile monoterpene that occurs naturally in sage, rosemary and carrot.

Application

• Based on HPLC and HS-GC-IMS Techniques, the Changes in the Internal Chemical Components of Schisandra chinensis (Turcz.) Baill. Fruit at Different Harvesting Periods Were Analyzed.: This study utilized high-performance liquid chromatography and headspace gas chromatography-ion mobility spectrometry to examine changes in internal chemical components, including terpinolene, of Schisandra chinensis during various harvest periods, offering insights into optimal harvest timing for maximum chemical efficacy (Sun et al., 2024).

• Exogenous methyl jasmonate treatment induced the transcriptional responses and accumulation of volatile terpenoids in Oenanthe javanica (Blume) DC.: Research focused on the effect of methyl jasmonate on the accumulation of volatile terpenoids, such as terpinolene, in Oenanthe javanica, demonstrating enhanced production of these compounds which are critical for plant defense mechanisms (Feng et al., 2024).