Ginsenoside Rg1

Ginsenoside Rg1
  • CAS No.:22427-39-0
Other grades of this product :
Ginsenoside Rg1 Basic information
Uses
Product Name:Ginsenoside Rg1
Synonyms:(3b,6a,12b)-3,12-dihydroxydammar-24-ene-6,20- diylbis(beta-d-glucopyranoside);(3beta,6alpha,12beta)-3,12-dihydroxydammar-24-ene-6,20-diylbis[beta-D-glucopyranoside];Ginsenoside Rg1 std.;Ginsenoside Rg1 (CAS# 22427-39-0);Gensenoside Rg1;GINSENOSIDE RG1 WITH HPLC;GINSENOSIDE-RG1 (GINSENOSIDE A2: GINSENOSIDE G1);dihydroxydammar-24-ene-6,20-diylbis-
CAS:22427-39-0
MF:C42H72O14
MW:801.01
EINECS:244-989-9
Product Categories:Inhibitors;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Saponins;The group of Ginsenosides;Ginsenoside series
Mol File:22427-39-0.mol
Ginsenoside Rg1 Chemical Properties
Melting point 194~197℃
Boiling point 898.5±65.0 °C(Predicted)
density 1.33±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility DMSO (Slightly), Methanol (Slightly), Pyridine (Slightly)
form neat
pka12.91±0.70(Predicted)
color White to Off-White
Stability:Hygroscopic
CAS DataBase Reference22427-39-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,T,F
Risk Statements 22-39/23/24/25-23/24/25-11
Safety Statements 2-45-36/37-16-7-24/25
WGK Germany 3
RTECS LY9537200
HS Code 29389090
MSDS Information
Ginsenoside Rg1 Usage And Synthesis
UsesGinsenoside Rg1 protects against arthitis through osteoclast differentiation inhibition. Anti-tumor agent, inhibits the NF-kB-dependant MMP-expression in PMA (phorbol myristate acetate)-induced tumor cell invasion.
Chemical PropertiesWhite solid
UsesGinsenoside Rg1 protects against arthitis through osteoclast differentiation inhibition. Anti-tumor agent, inhibits the NF-kB-dependant MMP-expression in PMA (phorbol myristate acetate)-induced tumor cell invasion.
DefinitionChEBI: A ginsenoside found in Panax ginseng and Panax japonicus var. major that is dammarane which is substituted by hydroxy groups at the 3beta, 6alpha, 12beta and 20 <ital pro-S positions, in which the hydroxy groups at positions 6 and 20 have been converted to the corresponding beta-D-glucopyranosides, and in which a double bond has been introduced at the 24-25 posit on.
Ginsenoside Rg1 Preparation Products And Raw materials

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