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Key Documents

91822

Supelco

5-Pentadecylresorcinol

analytical standard

Synonym(s):

1,3-Dihydroxy-5-pentadecylbenzene, 5-Pentadecyl-1,3-benzenediol

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About This Item

Empirical Formula (Hill Notation):
C21H36O2
CAS Number:
Molecular Weight:
320.51
Beilstein:
1982742
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

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grade

analytical standard

Quality Level

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

SMILES string

CCCCCCCCCCCCCCCc1cc(O)cc(O)c1

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

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This Item
GE17089102GE17089109P4937
Percoll® pH 8.5-9.5 (25 °C), suitable for cell culture

P4937

Percoll®

density

1.13 g/cm3

density

-

density

-

density

1.13 g/mL±0.005 g/mL at 25 °C (lit.)

packaging

pack of 1 L

packaging

pack of 250 mL

packaging

pack of 6 × 1 L

packaging

-

manufacturer/tradename

Cytiva 17-0891-01

manufacturer/tradename

Cytiva 17-0891-02

manufacturer/tradename

Cytiva 17-0891-09

manufacturer/tradename

-

color

Colorless to slightly yellow

color

Colorless to slightly yellow

color

Colorless to slightly yellow

color

-

pH range

8.5-9.5

pH range

8.5-9.5

pH range

8.5-9.5

pH range

-

General description

5-Pentadecylresorcinol is a resorcinol derivative[1], that can be found in the wood of Grevillea.banksii.[2]
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).[3]
  • Mango (Mangifera indica L.) peels using high-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (HPLC/APCI-MS).[4]

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.

Recommended products

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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    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
    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)
    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
    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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