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Merck
CN

W215805

Isoborneol

≥95%, FG

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About This Item

Empirical Formula (Hill Notation):
C10H18O
CAS Number:
124-76-5
Molecular Weight:
154.25
FEMA Number:
2158
Council of Europe no.:
2020
UNSPSC Code:
12164502
PubChem Substance ID:
24900674
EC Number:
204-712-4
Flavis number:
2.059
MDL number:
MFCD00074821
NACRES:
NA.21
Organoleptic:
woody; camphoraceous; balsamic
Grade:
FG, Fragrance grade, Halal, Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines, meets purity specifications of JECFA
Food allergen:
no known allergens

Key Documents

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grade

FG, Fragrance grade, Halal, Kosher

SMILES string

[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

InChI key

DTGKSKDOIYIVQL-MRTMQBJTSA-N

biological source

synthetic

agency

follows IFRA guidelines, meets purity specifications of JECFA

reg. compliance

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

description

Stabilized

assay

≥95%

contains

contains BHT, synthetic as stabilizer

mp

212-214 °C (subl.) (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

woody; camphoraceous; balsamic

Quality Level

400

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H228,H315

Hazard Classifications

Flam. Sol. 1 - Skin Irrit. 2

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 2

flash_point_f

200.1 °F - closed cup

flash_point_c

93.4 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ5356
STBJ3474
STBH8748
STBH9990
STBH3444

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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.
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)
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
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
Jingjing Liu et al.
European journal of pharmacology, 688(1-3), 1-5 (2011-12-28)
The bioavailabilities of eye drops are very low, so it is eager to find a safe and effective penetration enhancer to improve drug bioavailability. In our study, the corneas of New Zealand albino rabbit were mounted in the improved Franz
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