91822
5-Pentadecylresorcinol
analytical standard
Synonyme(s) :
1,3-Dihydroxy-5-pentadecylbenzene, 5-Pentadecyl-1,3-benzenediol
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A propos de cet article
Formule empirique (notation de Hill) :
C21H36O2
Numéro CAS:
Poids moléculaire :
320.51
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
221-599-7
Beilstein/REAXYS Number:
1982742
MDL number:
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Laissez-nous vous aiderInChI key
KVVSCMOUFCNCGX-UHFFFAOYSA-N
InChI
1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-16-20(22)18-21(23)17-19/h16-18,22-23H,2-15H2,1H3
SMILES string
CCCCCCCCCCCCCCCc1cc(O)cc(O)c1
grade
analytical standard
assay
≥95.0% (HPLC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
cleaning products
cosmetics
food and beverages
personal care
format
neat
storage temp.
2-8°C
Quality Level
General description
5-Pentadecylresorcinol is a resorcinol derivative, that can be found in the wood of Grevillea.banksii.
Occurs in peel and flesh of unripe mangos, Mangifera indica (Anacardiaceae).
Application
5-Pentadecylresorcinol has been used as an analytical reference standard for the quantification of the analyte in a mixture of alkylresorcinols using liquid chromatography coupled to mass spectrometry (LC-MS). It may also be used as an analytical reference standard for the determination of the analyte in:
- Goji berries using ultra-high-pressure liquid chromatography coupled with quadrupole-time-of-flight mass spectrometry (UHPLC-ESI-QTOF-MS).
- Mango (Mangifera indica L.) peels using high-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (HPLC/APCI-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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L Deszcz et al.
Biochimica et biophysica acta, 1483(2), 241-250 (2000-01-15)
The occurrence of alkylresorcinols, polyketide compounds that in the same homologous series as cardol isolated from Anacardium occidentale (cashew) or bilobol from Ginkgo biloba which are derivatives of 1,3-dihydroxy-5-alk(en)ylbenzene, have been demonstrated in developing rye (Secale cereale L.) kernels. The
Characterization of major and minor alk (en) ylresorcinols from mango (Mangifera indica L.) peels by high?performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry
Knodler M, et al.
Rapid Communications in Mass Spectrometry, 21(6), 945-951 (2007)
Leonardo Basso et al.
Plant physiology, 184(4), 2078-2090 (2020-09-27)
In angiosperms, the NADH dehydrogenase-like (NDH) complex mediates cyclic electron transport around PSI (CET). K+ Efflux Antiporter3 (KEA3) is a putative thylakoid H+/K+ antiporter and allows an increase in membrane potential at the expense of the ∆pH component of the
P Phani Kumar et al.
Journal of agricultural and food chemistry, 50(16), 4705-4708 (2002-07-26)
Commercially available technical cashew (Anacardium occidentale L.) nut shell liquid (CNSL) contains mainly cardanol (decarboxylated anacardic acid) and cardol. Cardanol, the monophenolic component of technical CNSL, is widely used as a synthon for the preparation of a number of polymers
Ta-Hsien Chuang et al.
Journal of natural products, 70(2), 319-323 (2007-01-25)
Bioassay-guided fractionation of the MeOH extract of the leaves of Grevillea robusta led to the isolation of six new 5-alkylresorcinols, gravicycle (1), dehydrogravicycle (2), bisgravillol (3), dehydrobisgravillol (4), dehydrograviphane (5), and methyldehydrograviphane (6), as well as eight known compounds. The
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