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trans-Sinapic acid

analytical standard

Synonyme(s) :

trans-4-Hydroxy-3,5-dimethoxy-cinnamic acid, trans-Sinapinic acid

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About This Item

Formule empirique (notation de Hill):
C11H12O5
Numéro CAS:
7362-37-0
Poids moléculaire :
224.21
Numéro CE :
208-487-3
Numéro MDL:
MFCD00004401
Code UNSPSC :
85151701
ID de substance PubChem :
329770283
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥99.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

195-205 °C (dec.)

Application(s)

food and beverages

Format

neat

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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Catégories apparentées

Application

trans-Sinapic acid may be used as an analytical reference standard for the quantification of the analyte in seed samples and vegetables using different chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Autres remarques

This compound is commonly found in plants of the genus: carum cinnamomum melissa salvia thymus zingiber

Produits recommandés

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.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCH4124
BCCD2885
BCBW0416
BCBR2570V
BCBL5966V

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Quantitation of free and hydrolyzable phenolic acids in seeds by capillary gas-liquid chromatography
Dabrowski.JK and Sosulski.WF
Journal of Agricultural and Food Chemistry, 32(1), 123-127 (1984)
Free and soluble bound phenolic acids in some cruciferous vegetables
Uda Y, et al.
Journal of the Japanese Society for Food Science and Technology, 35(5), 360-366 (1988)
Jacob C Dean et al.
Journal of the American Chemical Society, 136(42), 14780-14795 (2014-10-09)
Ultraviolet spectroscopy of sinapoyl malate, an essential UV-B screening agent in plants, was carried out in the cold, isolated environment of a supersonic expansion to explore its intrinsic UV spectral properties in detail. Despite these conditions, sinapoyl malate displays anomalous
Jiyan Liu et al.
Journal of ethnopharmacology, 155(2), 1322-1331 (2014-07-30)
Chemotherapy is the mainstay of modern tuberculosis (TB) control. Traditional Chinese Medicine (TCM) can enhance the effect of anti-TB drug, promote the absorption of the foci in the lung and reduce drug toxicity. In TCM, the determination of treatment is
Ivan K Baykov et al.
Vaccine, 32(29), 3589-3594 (2014-05-20)
The efficiency of several mouse monoclonal antibodies (mAbs) specific to the tick-borne encephalitis virus (TBEV) glycoprotein E in post-exposure prophylaxis was assessed, and mAb14D5 was shown to be the most active of all those studied. It was proven that the
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