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C80601

Sigma-Aldrich

Eucalyptol

greener alternative

99%

Synonym(s):

1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane, 1,8-Cineole, 1,8-Epoxy-p-menthane

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50 MG
$146.30
250 MG
$587.00

$146.30

List price$154.00
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50 MG
$146.30
250 MG
$587.00

About This Item

Empirical Formula (Hill Notation):
C10H18O
CAS Number:
470-82-6
Molecular Weight:
154.25
Beilstein/REAXYS Number:
105109
EC Number:
207-431-5
MDL number:
MFCD00167977
UNSPSC Code:
12352100
PubChem Substance ID:
24893017
NACRES:
NA.22

$146.30

List price$154.00
Web-Only Promotion

Available to ship onApril 09, 2025Details

Request a Bulk Order

Quality Level

200

assay

99%

form

liquid

greener alternative product characteristics

Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

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.)

greener alternative category

Aligned

SMILES string

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

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This Item
29210PHL89195W246506
Eucalyptol 99%

C80601

Eucalyptol

Eucalyptol analytical standard

29210

Eucalyptol

Eucalyptol phyproof® Reference Substance

PHL89195

Eucalyptol

Eucalyptol natural, ≥99%, FCC, FG

W246506

Eucalyptol

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

400

bp

176-177 °C (lit.)

bp

176-177 °C (lit.)

bp

176-177 °C (lit.)

bp

176-177 °C (lit.)

refractive index

n20/D 1.457 (lit.)

refractive index

n20/D 1.457 (lit.), n20/D 1.458

refractive index

n20/D 1.457 (lit.)

refractive index

n20/D 1.457 (lit.)

form

liquid

form

-

form

liquid

form

-

mp

1-2 °C (lit.)

mp

1-2 °C (lit.)

mp

1-2 °C (lit.)

mp

1-2 °C (lit.)

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. This product is a Biobased products, showing key improvements in Green Chemistry Principles “Use of Renewable Feedstock”.

Application

Eucalyptol undergoes pyrolysis to yield p-cymene and hydrogen gas.[1] It can be used in the synthesis of mosquito repellents[2] and herbicides.[3]

Pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

hcodes

H226,H317

Hazard Classifications

Flam. Liq. 3 - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

ppe

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

  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    BCCM4726
    BCCL1952
    BCCL1950
    BCCH9680
    BCCH7565

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    Production of p-cymene and hydrogen from a bio-renewable feedstock-1, 8-cineole (eucalyptus oil).
    Leita, Benjamin A et al.
    Green Chemistry, 12(1), 70-76 (2010)
    Preparation of biologically active substances and animal and microbial metabolites from menthols, cineoles and kauranes.
    Asakawa, Yoshinori et al.
    Phytochemistry, 27(12), 3861-3869 (1988)
    Herbicidal activity of cineole derivatives.
    Barton, Allan FM et al.
    Journal of Agricultural and Food Chemistry, 58(18), 10147-10155 (2010)
    Sara Invitto et al.
    Respiratory physiology & neurobiology, 259, 37-44 (2018-07-15)
    Obstructive Sleep Apnea Syndrome (OSA) is characterized by snoring associated with repeated apnea and/or obstructive hypopnea. The nasal airways of OSA patients, measured via acoustic rhinometry, could be significantly narrower than healthy subjects and this reduced nasal structure can impair
    Sara Invitto et al.
    Frontiers in aging neuroscience, 10, 272-272 (2018-10-03)
    Olfactory impairment is present in up to 90% of patients with Alzheimer's disease (AD) and is present in certain cases of mild cognitive impairment (MCI), a transient phase between normal aging and dementia. Subjects affected by MCI have a higher
    View All Related Papers

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