70158
(-)-桃金娘烯醇
analytical standard
别名:
(1R)-2-蒎烯-10-醇, (1R)-6,6-二甲基二环[3.1.1]庚-2-烯-2-甲醇
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关于此项目
经验公式（希尔记法）:
C10H16O
化学文摘社编号:
分子量:
152.23
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
243-409-1
Beilstein/REAXYS Number:
2206583
MDL number:
InChI key
RXBQNMWIQKOSCS-IUCAKERBSA-N
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
SMILES string
CC1(C)[C@H]2CC=C(CO)[C@@H]1C2
grade
analytical standard
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
Quality Level
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Other Notes
用作手性结构单元
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.
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.
存储类别
10 - Combustible liquids
wgk
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
R. Pellegata et al.
Helvetica Chimica Acta, 70, 71-71 (1987)
L. Borowiecki et al.
Liebigs Ann. Chem., 1775-1775 (1982)
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)
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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