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Merck
CN

W260401

Juniper berry oil

FG

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About This Item

CAS Number:
FEMA Number:
2604
UNSPSC Code:
12164502
NACRES:
NA.21
MDL number:
Organoleptic:
balsam; fresh; woody
Grade:
FG, Kosher
Biological source:
Juniperus communis L.
Food allergen:
no known allergens
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biological source

Juniperus communis L.

grade

FG, Kosher

reg. compliance

EU Regulation 1334/2008 & 178/2002, FDA 21 CFR 117, FDA 21 CFR 182.20

optical activity

[α]20/D −5.4°, neat

origin

southern Europe origin

refractive index

n20/D 1.479 (lit.)

bp

131-172 °C (lit.)

density

0.863 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

balsam; fresh; woody

Quality Level

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Biochem/physiol Actions

Taste at 10 ppm

Preparation Note

Extraction method: steam distillation

pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

109.9 °F - closed cup

flash_point_c

43.3 °C - closed cup

ppe

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

Regulatory Information

危险化学品
植物油/植物胶产品
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Elisabetta Gavini et al.
Pharmaceutical development and technology, 10(4), 479-487 (2005-12-24)
Solid lipid microparticles (SLM) were used as carriers of juniper oil and proposed for the topical treatment of acne vulgare. The formulations were obtained by the o/w emulsification method. Compritol and Precirol were employed as lipidic materials. Emulsions containing 1.5%
W Z Yang et al.
Journal of dairy science, 90(12), 5671-5681 (2007-11-21)
The objective of this study was to evaluate the effects of feeding essential oils from garlic (GAR) and juniper berry (JUN), or monensin (MO) on feed intake, ruminal fermentation, the site and extent of digestion, microbial protein synthesis, milk production
S R Chavali et al.
Prostaglandins, leukotrienes, and essential fatty acids, 59(2), 89-93 (1998-10-17)
Eicosapentaenoic acid (EPA) and the non-methylene interrupted fatty acids (NMIFA) displace arachidonic acid (AA: 20:4omega6 -5,8,11,14) in the membrane phospholipids. Unlike EPA (20:5omega3 -5,8,11,14,17), the NMIFA (20:3omega6 -5,11,14 and 20:4omega3 -5,11,14,17) lacking the delta-8 double bond are not substrates for
Lavjay Butani et al.
Transplantation, 76(2), 306-311 (2003-07-29)
Calcineurin-inhibitor nephrotoxicity plays a role in the pathogenesis of chronic allograft nephropathy by causing renal ischemia mediated by vasoconstrictive metabolites of the prostanoid pathway. The purpose of our study was to evaluate whether altering the prostanoid profile using juniper oil
Mosciano, G.
Perfumer & Flavorist, 27, 93-93 (2002)

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