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Rebaudioside D
CAS No. 63279-13-0
Rebaudioside D( —— )
Catalog No. M20282 CAS No. 63279-13-0
Rebaudioside D is a potential sweetener. Rebaudioside D shows similar stability when exposed to simulate stomach and small intestine fluids with susceptibility to hydrolytic degradation by enteric bacteria collected from the cecum.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 112 | In Stock |
|
| 2MG | 38 | In Stock |
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| 5MG | 56 | In Stock |
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| 10MG | 92 | In Stock |
|
| 25MG | 154 | In Stock |
|
| 50MG | 221 | In Stock |
|
| 100MG | 333 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 788 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameRebaudioside D
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NoteResearch use only, not for human use.
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Brief DescriptionRebaudioside D is a potential sweetener. Rebaudioside D shows similar stability when exposed to simulate stomach and small intestine fluids with susceptibility to hydrolytic degradation by enteric bacteria collected from the cecum.
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DescriptionRebaudioside D is a potential sweetener. Rebaudioside D shows similar stability when exposed to simulate stomach and small intestine fluids with susceptibility to hydrolytic degradation by enteric bacteria collected from the cecum.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number63279-13-0
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Formula Weight1129.2
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Molecular FormulaC50H80O28
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Purity>98% (HPLC)
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SolubilityDMSO:1mg/ml
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SMILES[H][C@@]12CC[C@@]3(C[C@]1(CC3=C)CC[C@]1([H])[C@@](C)(CCC[C@@]21C)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Purkayastha S Markosyan A Prakash I et al. Steviol glycosides in purified stevia leaf extract sharing the same metabolic fate[J]. Regulatory Toxicology and Pharmacology 2016 77:125-133.
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