Rebaudioside A structure, CAS 58543-16-1

Rebaudioside A

CAS Number58543-16-1

SynonymsTruvia; Stevioside A3; Rebaudioside A; rebiana

Molecular FormulaC44H70O23

Molecular Weight967.01

Purity98.00%

Density1.6±0.1 g/cm3

Boiling Point1102.8±65.0 °C at 760 mmHg

Melting Point242-244ºC

Flash Point

AppearanceSolid;White to Almost white powder to crystal

EINECS

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-9045016 Purity: 98.00%
Change View

Please Login or Create an Account to: See VlP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

Quality Control of [ 58543-16-1 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number58543-16-1
Catalog No.2A-9045016
Chinese Name甜菊双糖苷A
SynonymsTruvia; Stevioside A3; Rebaudioside A; rebiana
Molecular FormulaC44H70O23
Molecular Weight967.01
Purity98.00
Density1.6±0.1 g/cm3
Boiling Point1102.8±65.0 °C at 760 mmHg
Melting Point242-244ºC
AppearanceSolid;White to Almost white powder to crystal
Water SolubilityWater solubility: soluble
Storage ConditionStore in an airtight container in a dry, cool plac
ApplicationRebaudioside A is a steviol glycoside, α-glucosidase inhibitor, IC50 is 35.01 ug/mL
HTC29389090
PubChem ID12015932
SMILESC=C1CC23CCC4C(C)(C(=O)OC5OC(CO)C(O)C(O)C5O)CCCC4(C)C2CCC1(OC1OC(CO)C(O)C(OC2OC(CO)C(O)C(O)C2O)C1OC1OC(CO)C(O)C(O)C1O)C3
InChIInChI=1S/C44H70O23/c1-17-11-43-9-5-22-41(2,7-4-8-42(22,3)40(59)66-38-33(58)30(55)26(51)20(14-47)62-38)23(43)6-10-44(17,16-43)67-39-35(65-37-32(57)29(54)25(50)19(13-46)61-37)34(27(52)21(15-48)63-39)64-36-31(56)28(53)24(49)18(12-45)60-36/h18-39,45-58H,1,4-16H2,2-3H3/t18-,19-,20-,21-,22+,23+,24-,25-,26-,27-,28+,29+,30+,31-,32-,33-,34+,35-,36+,37+,38+,39+,41-,42-,43-,44+/m1/s1
InChI KeyHELXLJCILKEWJH-NCGAPWICSA-N
Hazard Symbolstransportation
BioactivityRebaudioside A is a steviol glycoside, α-glucosidase inhibitor with IC50 of 35.01 μg/ml.can inhibit ATP-sensitive K+-channels.Target: α-glucosidase [1]IC 50: 35.01 ug/mLIn vitro: rebaudioside A stimulat the insulin secretion from MIN6 cells in a dose- and glucose-dependent manner. In conclusion, the insulinotropic effect of rebaudioside A is mediated via inhibition of ATP-sensitive K+-channels and requires the presence of high glucose. [2]In vivo: in vivo mouse micronucleus test at doses up to 750 mg/kg bw and an unscheduled DNA synthesis test in rats at doses up to 2000 mg/kg bw, rebaudioside A do not cause any genotoxic effects at any of the doses tested.[3] Related Catalog Signaling Pathways >> Others >> Others Natural Products >> Terpenoids and Glycosides Research Areas >> Others References [1]. Adari BR et al. Synthesis of rebaudioside-A by enzymatic transglycosylation of stevioside present in the leaves of Stevia rebaudiana Bertoni. Food Chem. 2016 Jun 1;200:154-8. [2]. Abudula R et al. Rebaudioside A directly stimulates insulin secretion from pancreatic beta cells: a glucose-dependent action via inhibition of ATP-sensitive K-channels. Diabetes Obes Metab. 2008 Nov;10(11):1074-85. [3]. Williams LD et al. Genotoxicity studies on a high-purity rebaudioside A preparation. Food Chem Toxicol. 2009 Aug;47(8):1831-6. Chemical & Physical Properties Density 1.6±0.1 g/cm3 Boiling Point 1102.8±65.0 °C at 760 mmHg Melting Point 242-244ºC Molecular Formula C44H70O23 Molecular Weight 967.013 Flash Point 319.9±27.8 °C Exact Mass 966.430786 PSA 374.13000 LogP -1.13 Vapour Pressure 0.0±0.6 mmHg at 25°C Index of Refraction 1.659 InChIKey HELXLJCILKEWJH-NCGAPWICSA-N SMILES C=C1CC23CCC4C(C)(C(=O)OC5OC(CO)C(O)C(O)C5O)CCCC4(C)C2CCC1(OC1OC(CO)C(O)C(OC2OC(CO)C(O)C(O)C2O)C1OC1OC(CO)C(O)C(O)C1O)C3 Storage condition room temp
Use ofProperties Articles26 Name Rebaudioside A Synonym More Synonyms Rebaudioside A Biological Activity Related Catalog Signaling Pathways >> Others >> Others Natural Products >> Terpenoids and Glycosides Research Areas >> Others References [1]. Adari BR et al. Synthesis of rebaudioside-A by enzymatic transglycosylation of stevioside present in the leaves of Stevia rebaudiana Bertoni. Food Chem. 2016 Jun 1;200:154-8. [2]. Abudula R et al. Rebaudioside A directly stimulates insulin secretion from pancreatic beta cells: a glucose-dependent action via inhibition of ATP-sensitive K-channels. Diabetes Obes Metab. 2008 Nov;10(11):1074-85. [3]. Williams LD et al. Genotoxicity studies on a high-purity rebaudioside A preparation. Food Chem Toxicol. 2009 Aug;47(8):1831-6. Chemical & Physical Properties Molecular Formula C44H70O23 Exact Mass 966.430786 PSA 374.13000 LogP -1.13 Index of Refraction 1.659 InChIKey HELXLJCILKEWJH-NCGAPWICSA-N Storage condition room temp
Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
Related Products in Specialty Chemicals
1R,2R-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan58520-04-02A-9045008
(2-Pyridinyloxy)acetic acid58530-50-02A-0201490
3-Bromo-2-fluoronitrobenzene58534-94-42A-9045011
4-Hydroxy-2,6-dimethylbenzonitrile58537-99-82A-9045013
2-Methylnicotinamide58539-65-42A-9045015
Schisantherin A58546-56-82A-9045018
Carboprost tromethamine58551-69-22A-9045019
2,7-Dibromonaphthalene58556-75-52A-9045021
Tyrosylglycyl-glycyl-phenylalanyl-methionine58569-55-42A-9045023
Anagrelide hydrochloride58579-51-42A-9045027
Browse all Specialty Chemicals products »
Contact Us

Phone:

630-322-8886

630-322-8887

Email:

[email protected]

Office Locations:

Chicago, IL, USA

San Francisco, CA, USA