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Fórmula empírica (notación de Hill):
C15H14O6 · xH2O
Número CAS:
Peso molecular:
290.27 (anhydrous basis)
UNSPSC Code:
85151701
NACRES:
NA.79
PubChem Substance ID:
EC Number:
230-731-2
Beilstein/REAXYS Number:
92762
MDL number:
Assay:
≥96% (HPLC)
Form:
powder
Servicio técnico
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Permítanos ayudarleassay
≥96% (HPLC)
Quality Segment
form
powder
technique(s)
HPLC: suitable
color
white to light brown
mp
200 °C (decomposes on heating)
storage temp.
2-8°C
SMILES string
[H]O[H].O[C@H]1Cc2c(O)cc(O)cc2O[C@@H]1c3ccc(O)c(O)c3
InChI
1S/C15H14O6.H2O/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7;/h1-5,13,15-20H,6H2;1H2/t13-,15+;/m0./s1
InChI key
OFUMQWOJBVNKLR-NQQJLSKUSA-N
General description
Catechin is produced by Cutch tree and is abundantly found in tea leaves, grape seeds, vegetables and plant-based beverages. It is a plant-derived, polyphenolic anti-oxidant and acts as a plant secondary metabolite.
Application
(±)-Catechin hydrate has been used:
- to study its modulatory effect on drug resistance in human ovarian cancer cells
- to construct the standard curve of total flavonoid content
- to study its effects on the physiological parameters of Solanum lycopersicum
Biochem/physiol Actions
Polyphenolic antioxidant. Used in traditional Chinese medicine.
Catechin has phytotoxic properties. Racemic catechin may be used in studies on seed germination and plant invasiveness. Catechin and Epigallocatechin gallate (EGCG) may be used with other polyphenol flavonoids to study their effects in oxidation and peroxidation-related processes.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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