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Organoleptic:
balsam; fresh; woody
Grade:
FG, Kosher
Biological source:
Juniperus communis L.
Food allergen:
no known allergens
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
Biochem/physiol Actions
10ppm 时的味道
Preparation Note
提取方法:蒸馏
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3 - Skin Irrit. 2
存储类别
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
法规信息
危险化学品
植物油/植物胶产品
此项目有
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
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
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%
Mosciano, G.
Perfumer & Flavorist, 27, 93-93 (2002)
Albert Robbat et al.
Journal of chromatography. A, 1218(32), 5531-5541 (2011-07-12)
The complex nature of botanicals and essential oils makes it difficult to identify all of the constituents by gas chromatography/mass spectrometry (GC/MS) alone. In this paper, automated sequential, multidimensional gas chromatography/mass spectrometry (GC-GC/MS) was used to obtain a matrix-specific, retention
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