Stevioside

Modify Date: 2024-01-02 11:22:15

Stevioside Structure
Stevioside structure
 Common Name Stevioside
CAS Number 57817-89-7 Molecular Weight 804.872
Density 1.5±0.1 g/cm3 Boiling Point 963.3±65.0 °C at 760 mmHg
Molecular Formula C38H60O18 Melting Point 198°C
MSDS Chinese USA Flash Point 290.3±27.8 °C

 Use of Stevioside


Stevioside is a natural sweetener extracted from leaves of Stevia rebaudiana, with anticancer activity[1].

 Names

Name Stevioside
Synonym More Synonyms

 Stevioside Biological Activity

Description Stevioside is a natural sweetener extracted from leaves of Stevia rebaudiana, with anticancer activity[1].
Related Catalog
References

[1]. Khare N, et al. Stevioside mediated chemosensitization studies and cytotoxicity assay on breast cancer cell lines MDA-MB-231 and SKBR3. Saudi J Biol Sci. 2019 Nov;26(7):1596-1601.

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 963.3±65.0 °C at 760 mmHg
Melting Point 198°C
Molecular Formula C38H60O18
Molecular Weight 804.872
Flash Point 290.3±27.8 °C
Exact Mass 804.377991
PSA 294.98000
LogP 1.19
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.646
Storage condition 0-6°C

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NZ8175000
CHEMICAL NAME :
Kaur-16-en-18-oic acid, 13-((2-O-beta-D-glucopyranosyl-alpha-D-glucopyranosyl )oxy)-, beta- D-glucopyranosyl ester
CAS REGISTRY NUMBER :
57817-89-7
BEILSTEIN REFERENCE NO. :
0077427
LAST UPDATED :
199612
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C38-H60-O18
MOLECULAR WEIGHT :
804.98
WISWESSER LINE NOTATION :
L E6 B665 A 1B P OYTJ F1 J1 OU1 FVO- BT6OTJ CQ DQ EQ F1Q& NO- BT6OTJ DQ EQ F1Q CO- BT6OTJ CQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Sister chromatid exchange
TEST SYSTEM :
Rodent - hamster Fibroblast
DOSE/DURATION :
1 pph
REFERENCE :
HDSKEK Hiroshima Daigaku Sogo Kagakubu Kiyo, 4: Kiso, Kankyo Kagaku Kenkyu. Bulletin of the Faculty of Integrated Arts and Sciences, Hiroshima University, Series 4: Fundamental and Environmental Sciences. (1-1-89 Higashisenda-machi, Naka-ku, Hiroshima 730, Japan) V.6- 1980- Volume(issue)/page/year: 10,57,1985

 Safety Information

Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
RTECS NZ8175000
HS Code 2938909090

 Customs

HS Code 2938909090

 Articles32

More Articles
[Identification and biotransformation properties of a bacterium that converts stevioside into rubusoside].

Wei Sheng Wu Xue Bao 51(1) , 43-9, (2011)

The purpose of our study was to separate and identify a bacillus that could convert stevioside specifically. Then we identified the conversion product and studied the conversion capability of the baci...

Structures of the novel α-glucosyl linked diterpene glycosides from Stevia rebaudiana.

Carbohydr. Res. 346(13) , 2034-8, (2011)

From the commercial extract of the leaves of Stevia rebaudiana, two new minor diterpene glycosides having α-glucosyl linkage were isolated besides the known steviol glycosides including stevioside, st...

Mass production of rubusoside using a novel stevioside-specific β-glucosidase from Aspergillus aculeatus.

J. Agric. Food Chem. 60(24) , 6210-6, (2012)

Rubusoside (R) is a natural sweetener and a solubilizing agent with antiangiogenic and antiallergic properties. However, currently, its production is quite expensive, and therefore, we have investigat...

 Synonyms

Steviosides
EINECS 260-975-5
(1R,4S,5R,9S,10R,13S)-13-{[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxyméthyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yl]oxy}tétrahydro-2H-pyran-2-yl]oxy}-5,9-diméthyl-14-méthylènetétracyclo[11.2.1.0.0]hexadécane-5-carboxylate de (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yle
MFCD00079561
(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl-(1R,4S,5R,9S,10R,13S)-13-{[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-yl]oxy}-5,9-dimethyl-14-methylentetracyclo[11.2.1.0.0]hexadecan-5-carboxylat
1-O-[(5β,8α,9β,10α,13α)-13-{[2-O-(β-D-Glucopyranosyl)-β-D-glucopyranosyl]oxy}-18-oxokaur-16-en-18-yl]-β-D-glucopyranose
Steviosin
(4,α)-13-[(2-O-β-D-Glucopyranosylalpha-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid β-D-glucopyranosyl ester
Rebaudin
Stevioside
(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl (1R,4S,5R,9S,10R,13S)-13-{[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-yl]oxy}-5,9-dimethyl-14-methylenetetracyclo[11.2.1.0.0]hexadecane-5-carboxylate
1-O-{(5β,8α,9β,10α,13α)-13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-18-oxokaur-16-en-18-yl}-β-D-glucopyranose
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