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Sinapic acid

SIAL/85429 - matrix substance for MALDI-MS, ≥99.0% (T)

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

CAS Number: 530-59-6
Empirical Formula (Hill Notation): C11H12O5
Molecular Weight: 224.21
EC Number: 208-487-3
MDL Number: MFCD00004401
Linear Formula: C11H12O5
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-85429-1G 1 g
$91.00
1/EA
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45-85429-5G 5 g
$161.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 85429-1G

 

analyte chemical class(es) dendrimers, fullerenes, peptides, proteins
assay ≥99.0% (T)
cation traces Ba: ≤5 mg/kg
  Ca: ≤10 mg/kg
  Cd: ≤5 mg/kg
  Co: ≤5 mg/kg
  Cr: ≤5 mg/kg
  Cu: ≤5 mg/kg
  Fe: ≤20 mg/kg
  K: ≤50 mg/kg
  Mg: ≤5 mg/kg
  Mn: ≤5 mg/kg
  Na: ≤50 mg/kg
  Ni: ≤5 mg/kg
  Pb: ≤5 mg/kg
  Zn: ≤5 mg/kg
color slightly yellow
form powder
grade matrix substance for MALDI-MS
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+
InChI key PCMORTLOPMLEFB-ONEGZZNKSA-N
mp ~202 °C
Quality Level 100 
SMILES string COc1cc(C=CC(O)=O)cc(OC)c1O
solubility dioxane: 1 g/10 mL at Hot, clear to slightly hazy (Very Faint Yellow to Dark Yellow and Very Faint Orange to Dark Orange)
suitability in accordance for UV test
technique(s) MALDI-MS: suitable
Application: 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.
General description: Sinapic acid is a type of phenolic acid. 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.
Purity ≥99.0% (T)
mp ~202 °C
UNSPSC 12000000

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