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Steviol - ≥98%, high purity , CAS No.471-80-7

COA

Grade & Purity:

≥96%

Cas Number: 471-80-7
Molecular Weight: 318.5
MDL number: MFCD00210558
PubChem CID: 452967
PubChem SID: 504758893

In stock

Item Number

S138883

Grouped product items
SKU	Size	Availability	Price
S138883-5mg	5mg	3	$116.90
S138883-10mg	10mg	3	$198.90
S138883-25mg	25mg	2	$447.90
S138883-50mg	50mg	2	$805.90

View related series

Aquaporin (7) Ion channel (2197) Membrane Transporter/Ion Channel (1822)

Basic Description

Synonyms	Kaur-16-en-18-oic acid, 13-hydroxy-, (14-alpha)- \| (4R)-13-Hydroxykaur-16-en-18-oic acid \| J-525016 \| 4741LYX6RT \| SDCCGSBI-0633785.P001 \| Q426852 \| NCGC00186036-01 \| 13-Hydroxykaurenoic acid \| ent-13-Hydroxy-kauran-16-en-19-oic acid \| BDBM50480263 \| SCHE
Specifications & Purity	≥96%
Storage Temp	Protected from light,Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Prenol lipids
    - Subclass Diterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Prenol lipids
Subclass	Diterpenoids
Intermediate Tree Nodes	Not available
Direct Parent	Kaurane diterpenoids
Alternative Parents	Tertiary alcohols Cyclic alcohols and derivatives Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Kaurane diterpenoid - Tertiary alcohol - Cyclic alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

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RARA Tclin Retinoic acid receptor alpha (1324 Activities)

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Huh-7 (12904 Activities)

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MCF7 (126967 Activities)

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Raji (5516 Activities)

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A549 (127892 Activities)

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HCT-116 (91556 Activities)

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HepG2 (196354 Activities)

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HeLa (62764 Activities)

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MDA-MB-231 (73002 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)

Discover Target: pol

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Saccharomyces cerevisiae (19171 Activities)

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Mus musculus (284745 Activities)

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Calf thymus DNA (4845 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504758893
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504758893
IUPAC Name	(1R,4S,5R,9S,10R,13S)-13-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid
INCHI	InChI=1S/C20H30O3/c1-13-11-19-9-5-14-17(2,7-4-8-18(14,3)16(21)22)15(19)6-10-20(13,23)12-19/h14-15,23H,1,4-12H2,2-3H3,(H,21,22)/t14-,15-,17+,18+,19+,20-/m0/s1
InChIKey	QFVOYBUQQBFCRH-VQSWZGCSSA-N
Smiles	CC12CCCC(C1CCC34C2CCC(C3)(C(=C)C4)O)(C)C(=O)O
Isomeric SMILES	C[C@@]12CCC[C@@]([C@H]1CC[C@]34[C@H]2CC[C@](C3)(C(=C)C4)O)(C)C(=O)O
PubChem CID	452967
Molecular Weight	318.5

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number	Certificate Type	Date	Item
L2420431	Certificate of Analysis	Jan 04, 2025	S138883
K2222673	Certificate of Analysis	Sep 19, 2024	S138883
K2222678	Certificate of Analysis	Sep 19, 2024	S138883
K2222675	Certificate of Analysis	Sep 19, 2024	S138883
K2222857	Certificate of Analysis	Sep 19, 2024	S138883

Chemical and Physical Properties

Solubility	DMSO: >10 mg/mL
Sensitivity	light sensitive
Molecular Weight	318.400 g/mol
XLogP3	3.800
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	318.219 Da
Monoisotopic Mass	318.219 Da
Topological Polar Surface Area	57.500 Å²
Heavy Atom Count	23
Formal Charge	0
Complexity	583.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	6
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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Steviol - ≥98%, high purity , CAS No.471-80-7

Basic Description

Taxonomic Classification

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

Chemical and Physical Properties

Solution Calculators

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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