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Merck
CN

W509647

(−)-氧化石竹烯

95%

别名:

β-石竹烯环氧化物, (-)-环氧石竹烯, (1R,4R,6R,10S)-9-亚甲基-4,12,12-三甲基-5-氧杂三环[8.2.0.04,6]十二烷, 反式-石竹烯氧化物, 石竹素

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关于此项目

经验公式（希尔记法）:
C15H24O
化学文摘社编号:
1139-30-6
分子量:
220.35
Flavis number:
16.043
PubChem Substance ID:
24902045
UNSPSC Code:
12164502
FEMA Number:
4085
NACRES:
NA.21
EC Number:
214-519-7
MDL number:
MFCD00134216
Beilstein/REAXYS Number:
148213
Organoleptic:
woody
Grade:
Fragrance grade
Biological source:
synthetic
Agency:
follows IFRA guidelines
Food allergen:
no known allergens

主要文件

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产品名称

(−)-氧化石竹烯, 95%

InChI key

NVEQFIOZRFFVFW-RGCMKSIDSA-N

InChI

1S/C15H24O/c1-10-5-6-13-15(4,16-13)8-7-12-11(10)9-14(12,2)3/h11-13H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m1/s1

SMILES string

[H][C@@]12CCC(=C)[C@@]3([H])CC(C)(C)[C@]3([H])CC[C@@]1(C)O2

biological source

synthetic

grade

Fragrance grade

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009

assay

95%

optical activity

[α]20/D −70°, c = 2 in chloroform

mp

62-63 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

β-caryophyllene (ox.)

organoleptic

woody

Quality Level

300

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相关类别

Application


  • 氧化石竹烯与对乙酰氨基酚的协同镇痛作用及其相应的胃保护活性。: 这项研究表明，氧化石竹烯可以增强对乙酰氨基酚的止痛作用，同时具有胃保护作用，表明其在疼痛管理治疗中的潜力（Espinosa-Juárez et al., 2024）。


Disclaimer

仅供R&D或非EU食品使用不用于零售。

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBS8203
SHBP3967
SHBP0584
SHBN3479
SHBL7451

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Muhammad Iqbal Choudhary et al.
Journal of natural products, 69(10), 1429-1434 (2006-10-28)
Microbial transformation of the sesquiterpene (-)-caryophyllene oxide (1) [(1R,4R,5R,9S)-4,5-epoxycaryophyllan-8(13)-ene] by a number of fungi, using a standard two-stage fermentation technique, has afforded as products (1R,4R,5R,9S)-4,5-dihydroxycaryophyllan-8(13)-ene (2), (1S,4R,5R,8S,9S)-clovane-5,9-diol (3), (1R,4R,5R,9S,11R)-4,5-epoxycaryophyllan-8(13)-en-15-ol (4), (1R,4R,5R,9S,11S)-4,5-epoxycaryophyllan-8(13)-en-14-ol (5), (1R,2S,4R,5R,9S)-4,5-epoxy-13-norcaryophyllan-8-one (6), (1R,4R,5R,8S,9S)-4,5-epoxycaryophyllan-13-ol (7), (1R,4R,5R,8S, 9S,13S)-caryolane-5,8,13-triol (8), (1R,3R,4R,5R,8S,9S)-4,5-epoxycaryophyllan-3,13-diol
M Salomé Gachet et al.
Journal of natural products, 74(4), 559-566 (2011-03-29)
In a survey of plants from Ecuador with antiprotozoal activity, Cupania cinerea was found to show significant in vitro activity against the Plasmodium falciparum K1 strain and Trypanosoma brucei rhodesiense. Subsequently, activity-guided isolation of the n-hexane and dichloromethane extracts from
Fangfang Zeng et al.
Insect biochemistry and molecular biology, 113, 103213-103213 (2019-08-24)
Mosquitoes rely heavily on the olfactory system to find a host for a bloodmeal, plants for a source of energy and suitable sites for oviposition. Here, we examined a cluster of eight odorant receptors (ORs), which includes one OR, CquiOR1

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