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Merck
CN

03422

5-Tricosylresorcinol

analytical standard

Synonym(s):

1,3-Dihydroxy-5-tricosylbenzene, 5-Tricosyl-1,3-benzenediol, Tricosylresorcinol (23:0)

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About This Item

Empirical Formula (Hill Notation):
C29H52O2
CAS Number:
70110-60-0
Molecular Weight:
432.72
MDL number:
MFCD09743630
UNSPSC Code:
85151701
PubChem Substance ID:
329747631
NACRES:
NA.24

Key Documents

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grade

analytical standard

Quality Level

100

Assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CCCCCCCCCCCCCCCCCCCCCCCc1cc(O)cc(O)c1

InChI

1S/C29H52O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-27-24-28(30)26-29(31)25-27/h24-26,30-31H,2-23H2,1H3

InChI key

OHTBGMREZYLZQD-UHFFFAOYSA-N

General description

5-Tricosylresorcinol, belonging to the class of alkylresorcinols (ARs), is an important constituent of cereal grains. Alkylresorcinols exhibit anti-inflammatory, anti-tumor and anti-mutagenic properties, as studied from cell culture.

Application

5-Tricosylresorcinol may be used as an analytical reference standard in the following:
  • Quantification of the analyte in seeds using ultra-high performance liquid chromatography electrospray ionization coupled to quadrupole-time-of-flight mass spectrometry (UHPLC-ESI-QTOF-MS).       
  • Quantification of the analyte in Keishibukuryogan-ka-yokuinin Japanese medicine, using blood pharmacokinetic techniques.

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCH7966
BCCH0299
BCCF9429
BCCB8866
BCCB7668

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UHPLC-ESI-QTOF-MS screening of lignans and other phenolics in dry seeds for human consumption
Ghisoni S, et al.
Journal of functional foods, 34, 229-236 (2017)
Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients, 2 (2012)
Oral administration of the Japanese traditional medicine keishibukuryogan-ka-yokuinin decreases reactive oxygen metabolites in rat plasma: Identification of chemical constituents contributing to antioxidant activity
Matsubara Y, et al.
Molecules (Basel), 22(2), 256-256 (2017)
Alkylresorcinol composition allows the differentiation of Triticum spp. having different degrees of ploidy
Ziegler UJ, et al.
Journal of Cereal Science, 65, 244-251 (2015)
Yingdong Zhu et al.
Bioorganic & medicinal chemistry, 19(13), 3973-3982 (2011-06-11)
We and others have found that wheat bran oil is the active constituent in wheat bran for colon cancer prevention. However, the active components in wheat bran oil are still unknown. Using human colon cancer cells (HCT-116 and HT-29) as

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