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Merck
CN

W246506

桉树脑

natural, ≥99%, FCC, FG

别名:

1,3,3-三甲基-2-氧杂二环[2.2.2]辛烷, 1,8-桉叶素, 1,8-环氧对孟烷

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关于此项目

经验公式（希尔记法）:
C10H18O
化学文摘社编号:
470-82-6
分子量:
154.25
FEMA Number:
2465
Council of Europe no.:
182
UNSPSC Code:
12164502
PubChem Substance ID:
24901113
Flavis number:
3.001
EC Number:
207-431-5
NACRES:
NA.21
MDL number:
MFCD00167977
Beilstein/REAXYS Number:
105109
Organoleptic:
camphoraceous; herbaceous; minty
Grade:
FG, Fragrance grade, Halal, Kosher, natural
Agency:
follows IFRA guidelines, meets purity specifications of JECFA
Food allergen:
no known allergens

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grade

FG, Fragrance grade, Halal, Kosher, natural

SMILES string

C[C@]12CC[C@H](CC1)C(C)(C)O2

InChI key

WEEGYLXZBRQIMU-WAAGHKOSSA-N

InChI

1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3/t8-,10+

agency

follows IFRA guidelines, meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009, EU Regulation 1334/2008 & 178/2002, FCC, FDA 21 CFR 117

assay

≥99%

refractive index

n20/D 1.457 (lit.)

bp

176-177 °C (lit.)

mp

1-2 °C (lit.)

density

0.921 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

limonene (sum of D, L and DL)

organoleptic

camphoraceous; herbaceous; minty

Quality Level

300, 400

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相关类别

Biochem/physiol Actions

30ppm 时的味道

Other Notes

天然存在：小豆蔻、越橘、月桂、胡椒、迷迭香和甜马郁兰。

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

hcodes

H226,H317

Hazard Classifications

Flam. Liq. 3 - Skin Sens. 1

存储类别

3 - Flammable liquids

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBR3954
SHBR7228
SHBQ8824
SHBR0234
SHBP3781

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Hee-jin Jun et al.
Bioorganic & medicinal chemistry letters, 23(2), 579-583 (2012-12-19)
We investigated the effect of cineole on the expression of genes related to reverse cholesterol transport and hepatic fatty acid metabolism. Cineole, a small aroma compound in teas and herbs, significantly stimulated the transactivation of liver X receptor modulator (LXR)-α
Zerihun A Demissie et al.
Plant molecular biology, 79(4-5), 393-411 (2012-05-18)
Several members of the genus Lavandula produce valuable essential oils (EOs) that are primarily constituted of the low molecular weight isoprenoids, particularly monoterpenes. We isolated over 8,000 ESTs from the glandular trichomes of L. x intermedia flowers (where bulk of
Lisa A Shipley et al.
Journal of chemical ecology, 38(9), 1178-1189 (2012-10-12)
Pygmy rabbits (Brachylagus idahoensis) are one of only three vertebrates that subsist virtually exclusively on sagebrush (Artemisia spp.), which contains high levels of monoterpenes that can be toxic. We examined the mechanisms used by specialist pygmy rabbits to eliminate 1,8-cineole
Johannes F-W Greiner et al.
Biochimica et biophysica acta, 1833(12), 2866-2878 (2013-07-23)
Natural plant-derived products are commonly applied to treat a broad range of human diseases, including cancer as well as chronic and acute airway inflammation. In this regard, the monoterpene oxide 1,8-cineol, the active ingredient of the clinically approved drug Soledum®
Anke Fähnrich et al.
Plant molecular biology, 85(1-2), 135-145 (2014-02-05)
Nicotiana species of the section Alatae emit a characteristic floral scent comprising the' cineole cassette' monoterpenes 1,8-cineole, limonene, myrcene, β-pinene, α-pinene, sabinene and α-terpineol. All previously isolated 'cineole cassette'-monoterpene synthase genes are multi product enzymes that synthesize the seven compounds
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