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Merck
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Documenti fondamentali

W215805

Sigma-Aldrich

Isoborneol

≥95%, FG

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About This Item

Formula empirica (notazione di Hill):
C10H18O
Numero CAS:
Peso molecolare:
154.25
Numero FEMA:
2158
Numero CE:
N° CoE:
2020
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
2.059
Organolettico:
woody; camphoraceous; balsamic
Grado:
FG
Fragrance grade
Halal
Kosher
Origine biologica:
synthetic
agenzia:
follows IFRA guidelines
meets purity specifications of JECFA
Allergene alimentare:
no known allergens

Origine biologica

synthetic

Livello qualitativo

Grado

FG
Fragrance grade
Halal
Kosher

agenzia

follows IFRA guidelines
meets purity specifications of JECFA

Conformità normativa

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

Descrizione

Stabilized

Saggio

≥95%

contiene

contains BHT, synthetic as stabilizer

Punto di fusione

212-214 °C (subl.) (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Organolettico

woody; camphoraceous; balsamic

Stringa SMILE

[H][C@@]12CC[C@@](C)([C@H](O)C1)C2(C)C

InChI

1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1
DTGKSKDOIYIVQL-MRTMQBJTSA-N

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Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Flam. Sol. 1 - Skin Irrit. 2

Codice della classe di stoccaggio

4.1B - Flammable solid hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

200.1 °F - closed cup

Punto d’infiammabilità (°C)

93.4 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Sigma-Aldrich

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Camphene 95%

Sigma-Aldrich

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Camphene

D-Camphor ≥97%, FG

Sigma-Aldrich

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D-Camphor

Camphor (racemic) European Pharmacopoeia (EP) Reference Standard

C0405000

Camphor (racemic)

S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S182-S184 (2008-07-22)
A toxicologic and dermatologic review of isoborneol when used as a fragrance ingredient is presented.
Jianyu Su et al.
Journal of food science, 77(6), C658-C664 (2012-05-16)
The aims of this study were to optimize the preparation conditions of natural borneol/β-cyclodextrin (NB/β-CD) inclusion complex by ultrasound method, and to investigate its improvement of stability and solubility. The complex was characterized by different various spectroscopic techniques including Fourier
Rong Zhang et al.
European journal of drug metabolism and pharmacokinetics, 38(3), 159-169 (2013-04-17)
Borneol is a commonly used herbal medication in China and Japan. Previous studies have indicated that borneol could reduce the plasma concentrations of oneself and concomitant drugs, and its first-pass metabolism could be catalyzed by the cytochrome P450 3A (CYP3A)
Jinyoung Hur et al.
Pharmaceutical biology, 51(1), 30-35 (2012-11-09)
The β-amyloid (Aβ) peptide aggregation with accompanying oxidative stress plays the major role in the pathogenesis of Alzheimer's disease (AD). Some natural compounds, including borneol, shed promising light on AD treatment. The present study was designed to investigate the antioxidative
Fatiha El Babili et al.
Journal of medicinal food, 15(7), 671-676 (2012-05-23)
The volatile components from Croton campestris root bark were localized by an anatomical study and analyzed by gas chromatography-mass spectrometry for the first time. The roots of this plant showed secretory cells. These volatile constituents, isolated from the dichloromethane extract

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