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67563
3,4-Dihydroxy-5-methoxy-zimtsäure
≥95.0% (HPLC)
Synonym(e):
3-(3,4-Dihydroxy-5-methoxy-phenyl)-2-propensäure, 3-Methoxy-kaffeesäure, 5-Hydroxy-ferulasäure
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| Packungsgröße | SKU | Verfügbarkeit | Preis |
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Über diesen Artikel
Empirische Formel (Hill-System):
C10H10O5
CAS-Nummer:
Molekulargewicht:
210.18
UNSPSC Code:
12352106
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2697317
Preise und Verfügbarkeit sind derzeit nicht verfügbar.
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Unterstützung erhaltenQuality Segment
assay
≥95.0% (HPLC)
form
solid
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
SMILES string
COc1cc(\C=C\C(O)=O)cc(O)c1O
InChI
1S/C10H10O5/c1-15-8-5-6(2-3-9(12)13)4-7(11)10(8)14/h2-5,11,14H,1H3,(H,12,13)/b3-2+
InChI key
YFXWTVLDSKSYLW-NSCUHMNNSA-N
Biochem/physiol Actions
Secondary plant metabolite of the phenylpropanoid pathway.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
1 of 1
Dieser Artikel | |||
|---|---|---|---|
| assay ≥95.0% (HPLC) | assay ≥96.0% (T) | assay 97% | assay ≥98.0% (GC) |
| form solid | form powder | form solid | form powder |
| application(s) metabolomics | application(s) - | application(s) - | application(s) - |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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S Maury et al.
Plant physiology, 121(1), 215-224 (1999-09-11)
The biosynthesis of lignin monomers involves two methylation steps catalyzed by orthodiphenol-O-methyltransferases: caffeic acid/5-hydroxyferulic acid 3/5-O-methyltransferases (COMTs) and caffeoyl-coenzyme A (CoA)/5-hydroxyferuloyl-CoA 3/5-O-methyltransferases (CCoAOMTs). Two COMT classes (I and II) were already known to occur in tobacco (Nicotiana tabacum) and three
C C Chapple et al.
The Plant cell, 4(11), 1413-1424 (1992-11-01)
Mutants of Arabidopsis deficient in a major leaf phenylpropanoid ester, 2-O-sinapoyl-L-malate, were identified by thin-layer chromatographic screening of methanolic leaf extracts from several thousand mutagenized plants. Mutations at a locus designated SIN1 also eliminate accumulation of the sinapic acid esters
John M Humphreys et al.
Current opinion in plant biology, 5(3), 224-229 (2002-04-19)
Considerable interest in lignin biosynthesis has been fueled by the many roles that lignin plays in development and in resistance to biotic and abiotic stress, as well as its importance to industry and agriculture. Although the pathway leading to the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 67563-50MG | 04061832404875 |
| 67563-10MG | 04061832736020 |