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Capsanthin - Biochemical reagent, high purity , CAS No.465-42-9

2 Citations

COA

Grade & Purity:

Biochemical

Cas Number: 465-42-9
Molecular Weight: 584.87
MDL number: MFCD03423725
PubChem CID: 5281228
PubChem SID: 488195235

In stock

Item Number

C303766

Grouped product items
SKU	Size	Availability	Price
C303766-1g	1g	3	$9.90
C303766-5g	5g	3	$20.90
C303766-25g	25g	3	$80.90
C303766-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$290.90

Potent antioxidant

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Basic Description

Synonyms	AKOS040761459 \| Capsanthin, >=90.0% (HPLC) \| DTXSID10905012 \| (2E,4E,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen
Specifications & Purity	Biochemical
Biochemical and Physiological Mechanisms	Potent antioxidant. Main carotenoid in paprika. Active in vitro .
Storage Temp	Room temperature,Desiccated
Shipped In	Normal
Grade	Biochemical
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Prenol lipids
    - Subclass Tetraterpenoids
      - Level5 Carotenoids
        Level6 Xanthophylls

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Prenol lipids
Subclass	Tetraterpenoids
Intermediate Tree Nodes	Carotenoids
Direct Parent	Xanthophylls
Alternative Parents	Cyclopentanols Enones Acryloyl compounds Ketones Cyclic alcohols and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic homomonocyclic compounds
Substituents	Xanthophyll - Cyclopentanol - Alpha,beta-unsaturated ketone - Enone - Cyclic alcohol - Acryloyl-group - Secondary alcohol - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.
External Descriptors	C40 isoprenoids (tetraterpenes)
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)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

Discover Target: SLCO1B1

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

Associated Targets(non-human)

Rorc Nuclear receptor ROR-gamma (89407 Activities)

Discover Target: Rorc

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

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	488195235
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488195235
IUPAC Name	(2E,4E,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one
INCHI	InChI=1S/C40H56O3/c1-29(17-13-19-31(3)21-23-36-33(5)25-34(41)26-38(36,6)7)15-11-12-16-30(2)18-14-20-32(4)22-24-37(43)40(10)28-35(42)27-39(40,8)9/h11-24,34-35,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t34-,35+,40+/m1/s1
InChIKey	VYIRVAXUEZSDNC-RDJLEWNRSA-N
Smiles	CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C
Isomeric SMILES	CC1=C(C(C[C@@H](C1)O)(C)C)/C=C/C(=C/C=C/C(=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C(=O)[C@@]2(C[C@H](CC2(C)C)O)C)/C)/C
PubChem CID	5281228
Molecular Weight	584.87

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.

11 results found

Lot Number	Certificate Type	Date	Item
K2110366	Certificate of Analysis	Sep 09, 2024	C303766
K2110367	Certificate of Analysis	Sep 09, 2024	C303766
K2110388	Certificate of Analysis	Sep 09, 2024	C303766
G2415070	Certificate of Analysis	Jun 28, 2024	C303766
G2415071	Certificate of Analysis	Jun 28, 2024	C303766
G2415072	Certificate of Analysis	Jun 28, 2024	C303766
G2415073	Certificate of Analysis	Jun 28, 2024	C303766
D2408031	Certificate of Analysis	Oct 29, 2021	C303766
F2314368	Certificate of Analysis	Oct 29, 2021	C303766
F2314361	Certificate of Analysis	Oct 29, 2021	C303766
F2314367	Certificate of Analysis	Oct 29, 2021	C303766

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Chemical and Physical Properties

Molecular Weight	584.900 g/mol
XLogP3	10.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	11
Exact Mass	584.423 Da
Monoisotopic Mass	584.423 Da
Topological Polar Surface Area	57.500 Å²
Heavy Atom Count	43
Formal Charge	0
Complexity	1310.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	9
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	9
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Hongxia Wang, Chaoyang Wu, Juncheng Zhu, Yang Cheng, Yuxin Yang, Shihao Qiao, Bo Jiao, Liang Ma, Yu Fu, Hai Chen, Hongjie Dai, Yuhao Zhang. (2023) Stabilization of capsanthin in physically-connected hydrogels: Rheology property, self-recovering performance and syringe/screw-3D printing. CARBOHYDRATE POLYMERS, 319 (121209).
2. Jun Li, Xinyu Wu, Yue Chen, Junqian Deng, Hongping Yuan, Hailan Lian, Changlei Xia. (2024) Capsanthin-iodonium salt system for free radical photopolymerization under LED irradiation. DYES AND PIGMENTS, 230 (112347).

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