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W304603

Sigma-Aldrich

Terpinolene

≥95%, FG

Sinonimo/i:

4-isopropilidene-1-metilcicloesene, p-ment-1,4(8)-diene, p-met-1-en-8-il-formato

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About This Item

Formula empirica (notazione di Hill):
C10H16
Numero CAS:
Peso molecolare:
136.23
Numero FEMA:
3046
Beilstein:
1851203
Numero CE:
N° CoE:
2115
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
1.005
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

Grado

FG
Halal
Kosher

Conformità normativa

EU 1334/2008 & 872/2012

Densità del vapore

~4.7 (vs air)

Tensione di vapore

~0.5 mmHg ( 20 °C)

Saggio

≥95%

Indice di rifrazione

n20/D 1.489 (lit.)

P. eboll.

184-185 °C (lit.)

Densità

0.861 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

fresh; woody; citrus; pine; sweet

Stringa SMILE

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
MOYAFQVGZZPNRA-UHFFFAOYSA-N

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Descrizione generale

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

Applicazioni


  • 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).


Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 3 - Asp. Tox. 1 - Skin Sens. 1

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

141.8 °F - Seta closed cup

Punto d’infiammabilità (°C)

61 °C - Seta closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificati d'analisi (COA)

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Sigma-Aldrich

W530597

Sabinene

Terpineolo mixture of isomers, 96%, FG

Sigma-Aldrich

W304506

Terpineolo

γ-Terpinene natural, 95%, FG

Sigma-Aldrich

W355901

γ-Terpinene

α-Terpinene ≥89%, FCC, FG

Sigma-Aldrich

W355801

α-Terpinene

Terpinolene, a component of herbal sage, downregulates AKT1 expression in K562 cells.
Okumura N, et al
Oncology Letters, 3(2), 321-324 (2012)
Carrot flavor: effects of genotype, growing conditions, storage, and processing.
Simon PW.
Evaluation of quality of fruits and vegetables, 315-328 (1985)
John H Borden et al.
Journal of economic entomology, 101(4), 1266-1275 (2008-09-05)
The superiority of the host monoterpene myrcene as a synergist for trans-verbenol and exo-brevicomin, aggregation pheromone components of the mountain pine beetle, Dendroctonus ponderosae Hopkins (Coleoptera: Curculionidae), suggests that the ancestral host of the mountain pine beetle is a pine
Michael Russell et al.
Phytochemistry, 59(7), 709-716 (2002-03-23)
Individual leaves of the commercial terpinen-4-ol type of Melaleuca alternifolia were examined both quantitatively and qualitatively for volatile constituents from the emergence of the first true leaves, through to 6-week-old tenth leaf set material. A GC internal standard addition method
J Grassmann et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 12(6-7), 416-423 (2005-07-13)
Antioxidants from several nutrients, e.g. vitamin E, beta-carotene, or flavonoids, inhibit the oxidative modification of low-density lipoproteins. This protective effect could possibly retard atherogenesis and in consequence avoid coronary heart diseases. Some studies have shown a positive effect of those

Articoli

-Cymene; Linalool; Menthol; α-Terpineol; Menthyl acetate

Protocolli

-Cymene; (−)-Menthone; α-Terpineol, natural, ≥96%, FCC, FG; Terpinolene; β-Bourbonene; 1-Octen-3-ol; β-Caryophyllene; Linalool; α-Terpinene; (−)-Menthol

-α-Bergamotene; β-Bisabolene; α-Terpineol; Neryl acetate; Geranyl acetate; Neral; Geranial

Cymene; 4,5,6,7-Tetrahydro-3,6-dimethylbenzofuran; Linalool; Menthol; Menthone; Menthyl acetate; Germacrene D; Bicyclogermacrene; Thymol

-3,7-Dimethyl-2,6-octadien-1-ol; Neral; Geraniol; Geranial; Undecanal; Citronellyl acetate; Neryl acetate; 3,7-Dimethyl-2,6-octadienyl acetate; 1-Tetradecene; Tetradecane; α-Bisabolol

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