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70158

Supelco

(−)-Myrtenol

analytical standard

Synonym(s):

(1R)-2-Pinen-10-ol, (1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-methanol

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
Molecular Weight:
152.23
Beilstein/REAXYS Number:
2206583
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥98.5% (sum of enantiomers, GC)

optical activity

[α]/D -56±1°, c = 1 in chloroform

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.496

bp

220-222 °C (lit.)

density

0.981 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CC1(C)[C@H]2CC=C(CO)[C@@H]1C2

InChI

1S/C10H16O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h3,8-9,11H,4-6H2,1-2H3/t8-,9-/m0/s1

InChI key

RXBQNMWIQKOSCS-IUCAKERBSA-N

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General description

(−)-Myrtenol is a naturally occurring monoterpene alcohol, belonging to the class of volatile organic compounds. It is widely used in fragrance, cosmetic products, cleaning agents and flavoring agents in a variety of food products.

Application

(−)-Myrtenol may be used as an analytical reference standard for the quantification of the analyte in biological samples using high-performance liquid chromatography with fluorescence detection and electrospray ionization-mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Use as chiral building block

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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R. Pellegata et al.
Helvetica Chimica Acta, 70, 71-71 (1987)
Sensitive determination of monoterpene alcohols in urine by HPLC-FLD combined with ESI-MS detection after online-solid phase extraction of the monoterpene-coumarincarbamate derivates
Meesters.W.JR, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 875(2), 444-450 (2008)
Y. Bounameaux et al.
Helvetica Chimica Acta, 66, 989-989 (1983)
L. Borowiecki et al.
Liebigs Ann. Chem., 1775-1775 (1982)
Synthesis of stable thromboxane A2 analogs: pinane thromboxane A2 (PTA2) and carbocyclic thromboxane A2 (CTA2).
K C Nicolaou et al.
Methods in enzymology, 86, 400-409 (1982-01-01)

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