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Sinapic acid

matrix substance for MALDI-MS, ≥99.5%, Ultra pure

Synonyme(s) :

3,5-Dimethoxy-4-hydroxycinnamic acid, 4-Hydroxy-3,5-dimethoxy-cinnamic acid, Sinapinic acid

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About This Item

Formule empirique (notation de Hill):
C11H12O5
Numéro CAS:
Poids moléculaire :
224.21
Numéro Beilstein :
2699118
Numéro CE :
Numéro MDL:
Code UNSPSC :
12000000
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Qualité

matrix substance for MALDI-MS

Niveau de qualité

Pureté

≥99.5% (HPLC)
≥99.5%

Classe(s) chimique(s) de l'analyte

dendrimers, fullerenes, peptides, proteins

Technique(s)

MALDI-MS: suitable

Pf

~202 °C

Solubilité

dioxane: 1 g/10 mL at hot, clear, faintly yellow to yellow

Traces de cations

Al: ≤1 mg/kg
Ba: ≤1 mg/kg
Ca: ≤2 mg/kg
Cd: ≤1 mg/kg
Co: ≤1 mg/kg
Cr: ≤1 mg/kg
Cu: ≤1 mg/kg
Fe: ≤1 mg/kg
K: ≤2 mg/kg
Li: ≤1 mg/kg
Mg: ≤1 mg/kg
Mn: ≤1 mg/kg
Na: ≤2 mg/kg
Ni: ≤1 mg/kg
Sr: ≤1 mg/kg
Zn: ≤1 mg/kg

Adéquation

in accordance for UV test

Chaîne SMILES 

COc1cc(\C=C\C(O)=O)cc(OC)c1O

InChI

1S/C11H12O5/c1-15-8-5-7(3-4-10(12)13)6-9(16-2)11(8)14/h3-6,14H,1-2H3,(H,12,13)/b4-3+

Clé InChI

PCMORTLOPMLEFB-ONEGZZNKSA-N

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Description générale

Sinapic acid is one of the 4 most common hydroxycinnamic acids. It is widespread in the plant kingdom (vegetables, fruits, oilseed crops, cereal grains and medicinal plants, and some spices). It is mostly found in the form of esters, but may exist in the free form too.

Application


  • Metabolic Fate Characterization: Sinapic acid′s metabolic fate in biological systems is a significant area of research. Recent studies in rats have focused on identifying the metabolic pathways and by-products of sinapic acid, using advanced techniques such as liquid chromatography-mass spectrometry (LC-MS). These studies provide insights into its bioavailability and pharmacokinetics, which are crucial for understanding its therapeutic potential (Analytical and Bioanalytical Chemistry, 2023).

  • Efficient Extraction from Plant Materials: Sinapic acid is extracted from various plant sources using molecularly imprinted polymers (MIPs) and deep eutectic solvents. These methods enhance the efficiency and selectivity of sinapic acid extraction, making it a valuable approach for analytical chemists working on natural product isolation and characterization. This application is particularly relevant in the food and pharmaceutical industries for quality control and standardization (Food Chemistry, 2023).

  • Selective Sensing Applications: Sinapic acid is used in the development of nanocomposites for selective sensing applications. For instance, Ni-sinapic acid nanocomposites have been developed for the selective detection of permanganate ions. This research showcases the versatility of sinapic acid in creating sensitive and specific sensors for environmental monitoring and analytical applications (Journal of Photochemistry and Photobiology A: Chemistry, 2023).

  • Bioactivity Studies: The bioactivity of sinapic acid extends to its anti-inflammatory and anticancer properties. Studies have shown that sinapic acid can modulate various biochemical pathways, providing protective effects against inflammation and cancer. These findings underscore its potential as a bioactive compound in therapeutic formulations and highlight the importance of analytical methods in quantifying its efficacy and safety (Stem Cell Research International, 2022).

Actions biochimiques/physiologiques

On removal of amino group from phenylalanine, catalysing with enzyme phenylalanine ammonia-lyase forms cinnamic acid. The precursor of hydroxycinnamates is produced after hydroxylation of benzene ring. One of the precursors produced is sinapic acid. Sinapic acid exhibits antimicrobial, antioxidant, anticancer, anti-inflammatory, and anti-anxiety activity. Sinapine (sinapoyl choline) has been acknowledged as an acetylcholinesterase inhibitor, making it therapeutically applicable in treatment of various diseases. 4-Vinylsyringol (a decarboxylation product of sinapic acid) is a potent antimutagenic and antioxidative agent, involved in suppressing the induction of inflammatory cytokines and carcinogenesis. Owing to their anti-oxidative activity, these compounds have been considered to be potentially employed in the pharmaceutical industry, cosmetics and food processing.
Sinapic acid was suitable as phenolic standard for HPLC analysis in determination of Sinapic acid derivatives in Canola extracts. 10 g/L of sinapinic acid with solvent was suitable as matrix for ultraviolet laser desorption mass spectrometric determination of proteins. It was also suitable to use as matrix for MALDI-TOFMS and MALDI-ion mobility-TOFMS to determine phospholipids in tissue.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Determination of sinapic acid derivatives in canola extracts using high-performance liquid chromatography.
Khattab, Rabie, et al.
Journal of the American Oil Chemists' Society, 87 (2), 147-155 (2010)
Sinapic acid and its derivatives: natural sources and bioactivity.
Niciforovic, Neda, and Helena Abramovic
Comprehensive Reviews in Food Science and Food Safety, 13 (1), 34-51 (2014)
Cinnamic acid derivatives as matrices for ultraviolet laser desorption mass spectrometry of proteins.
Beavis, Ronald C., Brain T. Chait, and H. M. Fales.
Rapid Communications in Mass Spectrometry, 3 (12), 432-435 (1989)
Climate change and crops
Singh, S. N., ed.
Springer Science & Business Media (2009)
Direct tissue analysis of phospholipids in rat brain using MALDI-TOFMS and MALDI-ion mobility-TOFMS
Jackson SN, Wang HY, Woods AS, Ugarov M, Egan T, Schultz JA.
Journal of the American Society For Mass Spectrometry, 16 (2), 133-138 (2005)

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