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Sennoside B

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Sennoside B Basic information

Product Name:
Sennoside B
Synonyms:
  • PURSENNIDE
  • SENNOSIDE B 96.5+%
  • Sennoside B std.
  • 9,9-Bianthracene-2,2-dicarboxylic acid, 5,5-bis(.beta.-D-glucopyranosyloxy)-9,9,10,10-tetrahydro-4,4-dihydroxy-10,10-dioxo-, (9R,9S)-
  • (9S)-9-[(9R)-2-carboxy-4-hydroxy-10-oxo-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-anthracen-9-yl]-4-hydroxy-10-oxo-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9H-anthracene-2-carboxylic acid
  • SENNIDINE B(RG)
  • SENNOSIDE B(P)
  • SENNOSIDE B(SH)
CAS:
128-57-4
MF:
C42H38O20
MW:
862.74
EINECS:
204-895-0
Product Categories:
  • The group of Sennosides
  • Anthraquinones, Hydroquinones and Quinones
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Inhibitors
Mol File:
128-57-4.mol
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Sennoside B Chemical Properties

Melting point:
209~212℃
alpha 
D20 -100° (c = 0.2 in 70% acetone); D20 -67° (c = 0.4 in 70% dioxane)
Boiling point:
698.48°C (rough estimate)
Density 
1.3066 (rough estimate)
refractive index 
1.7630 (estimate)
storage temp. 
2-8°C
solubility 
DMSO (Very Slightly, Heated), Methanol (Slightly, Heated)
pka
3.31±0.40(Predicted)
form 
Solid
color 
Light Yellow to Dark Yellow
BRN 
5723747
Stability:
Hygroscopic
LogP
1.880 (est)
CAS DataBase Reference
128-57-4(CAS DataBase Reference)
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Safety Information

Risk Statements 
22
Safety Statements 
22-45-24/25
WGK Germany 
3
HS Code 
29329990
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Sennoside B Usage And Synthesis

Chemical Properties

White to brown powder

Uses

Sennoside B is used in the inhibition of platelet driven growth factor (PDGF) used and may inhibit proliferative disease which depend upon the PDGF pathway. Laxative.

Definition

ChEBI: A member of the class of sennosides that is (9R,9'S)-9,9',10,10'-tetrahydro-9,9'-bianthracene-2,2'-dicarboxylic acid which is substituted by hydroxy groups at positions 4 and 4', by beta-D glucopyranosyloxy groups at positions 5 and 5', and by oxo groups at positions 10 and 10'.

Purification Methods

Sennoside B forms yellow crystals from aqueous acetone or large volumes of H2O. [Stoll et al. Helv Chim Acta 32 1896 1900, Beilstein 17 III/IV 3402.]

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