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BETA2-CHACONINE is a naturally occurring steroidal alkaloid found in the Solanaceae plant family, particularly in potatoes (Solanum tuberosum) and tomatoes (Solanum lycopersicum). It is one of the glycoalkaloids, which are secondary metabolites produced by plants as a defense mechanism against herbivores and pathogens. Beta2-chaconine is structurally similar to solanine, another glycoalkaloid, and both are known for their bitter taste and potential toxicity when consumed in large quantities. While they play a role in plant defense, excessive intake of these compounds in humans can lead to gastrointestinal issues and, in severe cases, poisoning. The concentration of beta2-chaconine and other glycoalkaloids in potatoes and tomatoes is generally low and not harmful when consumed as part of a balanced diet. However, it is important to avoid consuming green or sprouted potatoes, as their glycoalkaloid content can increase significantly, posing a health risk.

469-14-7

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469-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 469-14-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 469-14:
(5*4)+(4*6)+(3*9)+(2*1)+(1*4)=77
77 % 10 = 7
So 469-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C39H63NO10/c1-18-6-9-26-19(2)29-27(40(26)16-18)15-25-23-8-7-21-14-22(10-12-38(21,4)24(23)11-13-39(25,29)5)48-37-34(46)32(44)35(28(17-41)49-37)50-36-33(45)31(43)30(42)20(3)47-36/h7,18-20,22-37,41-46H,6,8-17H2,1-5H3/t18-,19+,20-,22?,23+,24?,25-,26+,27-,28+,29-,30-,31+,32+,33+,34+,35+,36-,37+,38-,39-/m0/s1

469-14-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name solanidine 3-O-α-L-rhamnopyranosyl-(1->4)-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names β2-chaconine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:469-14-7 SDS

469-14-7Relevant academic research and scientific papers

Thermal Degradation of Glycosides, V - Hydrothermolysis of Triterpenoid and Steroid Glycosides

Kim, Youn Chul,Higuchi, Ryuichi,Komori, Tetsuya

, p. 453 - 460 (2007/10/02)

In this paper the hydrothermolysis of triterpenoid and steroid glycosides is described.By mere heating with water or water/1,4-dioxane solution, the triterpenoid and steroid glycosides 1, 4 and 15, 16, 25, 29, respectively, are converted into their aglycones and prosapogenins.Furthermore, hydrothermolysis of the triterpenoid 3,28-O-bisglycosides 5, 6, 8, 9, 12 affords the corresponding 3-O-glycosides and reduced oligosaccharides formed by selective cleavage of the ester glycosidic linkage.It is expected that this hydrothermolysis is useful for the structure determination of some triterpenoid and steroid glycosides and for yielding new oligosaccharides.The hydrothermolyzed products have been isolated by chromatography and their structures elucidated by spectroscopic methods.Key Words: Degradation, thermal / Thermolysis / Glycosides / Carbohydrates / Triterpenoids / Steroids

ALKALOIDS OF Rhinopetalum stenantherum. II. THE STRUCTURE OF STENANTHINE AND STENANTHIDINE

Samikov, K.,Rashkes, Ya. V.,Shakirov, R.,Yunusov, S. Yu.

, p. 273 - 278 (2007/10/02)

From a methanolic extract of the epigeal part of Rhinopetalum stenantherum have been isolated β-chaconine (I) and the new glucoalkaloids stenanthine with mp 262-264 deg C, D 46.5 deg, C45H73NO13 (II), and stenanthidine with mp 269-271 deg C, D -47.5 deg, C39H63NO11 (III).On the basis of the facts that partial hydrolysis of trioside (II) formed the biosides (I) and (III), and that on the hydrolysis of the latter the monoside γ-chaconine was found, it may be assumed that stenanthine has the structure of solanidine 3-O-(--D-glucoside), and stenanthidine that of solanidine 3-O-.

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