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Key Documents

W506907

Sigma-Aldrich

(1S)-(−)-Verbenone

≥93%

Sinônimo(s):

(1S,5S)-2-Pinen-4-one, (1S,5S)-4,6,6-Trimethylbicyclo[3.1.1]hept-3-en-2-one

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About This Item

Fórmula empírica (Notação de Hill):
C10H14O
Número CAS:
Peso molecular:
150.22
Beilstein:
1907623
Número CE:
Número MDL:
Código UNSPSC:
12164502
ID de substância PubChem:
NACRES:
NA.21

fonte biológica

synthetic

Nível de qualidade

grau

Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

conformidade reg.

EU Regulation 1223/2009

Ensaio

≥93%

atividade óptica

[α]20/D −140°, c = 10 in ethanol

índice de refração

n20/D 1.496 (lit.)

pb

227-228 °C (lit.)

densidade

0.975 g/mL at 20 °C (lit.)

aplicação(ões)

flavors and fragrances

Documentação

see Safety & Documentation for available documents

alérgeno alimentar

no known allergens

alérgeno de fragrância

no known allergens

Organoléptico

camphoraceous; minty; spicy

cadeia de caracteres SMILES

CC1=CC(=O)[C@H]2C[C@@H]1C2(C)C

InChI

1S/C10H14O/c1-6-4-9(11)8-5-7(6)10(8,2)3/h4,7-8H,5H2,1-3H3/t7-,8+/m0/s1

chave InChI

DCSCXTJOXBUFGB-JGVFFNPUSA-N

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Categorias relacionadas

Aplicação

  • Anti-Inflammatory and Antinociceptive Activities of the Essential Oil of Tagetes parryi A. Gray (Asteraceae) and Verbenone.: This article reports on the anti-inflammatory and pain-relief effects of (1S)-(−)-Verbenone as part of the essential oil of Tagetes parryi, suggesting potential therapeutic applications for pain management and inflammation (González-Velasco et al., 2022).

Exoneração de responsabilidade

For R&D or non-EU Food use. Not for retail sale.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

185.0 °F - closed cup

Ponto de fulgor (°C)

85 °C - closed cup

Equipamento de proteção individual

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


Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Chirality, 31(10), 865-869 (2019-08-09)
R/S mixture of monoterpene alcohol cis-verbenol can be separated in preparative scale by its conversion into phthalic mono-ester and subsequent crystallization of its diastereomeric salts with (R)-α-methylbenzylamine and (S)-α-methylbenzylamine. Finally, basic methanolysis of the resolved phthalic mono-esters results (S)-cis-verbenol and
Deepa S Pureswaran et al.
Journal of economic entomology, 105(1), 140-148 (2012-03-17)
We collected, identified, and quantified volatiles arising from individual gallery entrances of the monogamous bark beetle Dendroctonus frontalis Zimmermann. Samples were collected while the insects were mass attacking mature loblolly pines (Pinus taeda L.) in an established infestation in western
Christopher J Fettig et al.
Journal of economic entomology, 105(1), 149-160 (2012-03-17)
Currently, techniques for managing western pine beetle, Dendroctonus brevicomis LeConte (Coleoptera: Curculionidae, Scolytinae), infestations are limited to tree removals (thinning) that reduce stand density and presumably host susceptibility, and/or the use of insecticides to protect individual trees. There continues to
Nancy E Gillette et al.
Environmental entomology, 41(6), 1575-1586 (2013-01-17)
In an attempt to improve semiochemical-based treatments for protecting forest stands from bark beetle attack, we compared push-pull versus push-only tactics for protecting lodgepole pine (Pinus contorta Douglas ex Loudon) and whitebark pine (Pinus albicaulis Engelm.) stands from attack by
Zulfa Yoosuf-Aly et al.
Chemical communications (Cambridge, England), 48(56), 7040-7042 (2012-06-12)
The enzyme-guided asymmetric synthesis of (+)-verbenone from geranyl diphosphate in a simple two-step, one pot transformation highlights the potential of chemoenzymatic procedures for the generation of high-value terpenoids.

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