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CYMARIN

Product Name
CYMARIN
CAS No.
508-77-0
Chemical Name
CYMARIN
Synonyms
CYMARIN;CIMARIN;KOMBETIN;CYMARINE;WV-90043a;alvonalmr;CYMARIN(P);K STROPHANTHIN;STROPHANTHIN K;K-STROPHANTHIN-A
CBNumber
CB4291060
Molecular Formula
C30H44O9
Formula Weight
548.66
MOL File
508-77-0.mol
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CYMARIN Property

Melting point:
148°C
alpha 
D20 +39.2° (methanol); D22 +39.0° (c = 1.7 in chloroform)
Boiling point:
540.83°C (rough estimate)
Density 
1.1277 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
2-8°C
form 
Solid
pka
13.55±0.70(Predicted)
color 
White to off-white
BRN 
101370
LogP
0.640
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Safety

Hazard Codes 
T,T+
Risk Statements 
23/25-33-26/27/28-41
Safety Statements 
45-36/37/39-36/37-28-26
RIDADR 
UN 3462 6.1/PG 2
WGK Germany 
3
RTECS 
GZ5600000
8-10-23
HazardClass 
6.1(b)
PackingGroup 
III
Toxicity
LD50 i.v. in rats: 24.8±1.8 mg/kg (Vogel, Kluge)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H373May cause damage to organs through prolonged or repeated exposure

Precautionary statements

P314Get medical advice/attention if you feel unwell.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
30030
Product name
Cymarin
Purity
≥96% (HPLC)
Packaging
5mg
Price
$203.2
Updated
2024/03/01
Sigma-Aldrich
Product number
30030
Product name
Cymarin
Purity
≥96% (HPLC)
Packaging
1mg
Price
$144
Updated
2023/06/20
Sigma-Aldrich
Product number
PHL89838
Product name
Cymarin
Purity
phyproof Reference Substance
Packaging
20mg
Price
$425
Updated
2024/03/01
TRC
Product number
C989908
Product name
Cymarin
Packaging
5mg
Price
$540
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC156960
Product name
Cymarin
Packaging
500ug
Price
$125
Updated
2021/12/16
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CYMARIN Chemical Properties,Usage,Production

Originator

Alvonal,Goumldecke

Uses

Cymarin is a pure allelochemicals that is a potent growth inhibitor in plants.

Uses

Cymarin was used to study the effect of cardiac glycosides on vascular smooth muscles and ion transport.

Definition

ChEBI: Cymarin is a cardenolide glycoside.

Manufacturing Process

Finely ground seeds of Castilloa elastica (3550 g) are percolated with sufficient light petroleum (boiling point 60°-80°C) to ensure removal of all the fat. The mart is dried with a current of air and percolated with chloroform until no further color is obtained with alkaline m-dinitrobenzene. The percolate is evaporated under reduced pressure, the residue triturated with dry ether (750 ml) and filtered. The residue (69.75 g) is washed with dry ether, dried, and some of the washed residue (20 g) is dissolved in a benzene-chloroform mixture (50 ml), comprising one part benzene to two parts chloroform by volume, and is absorbed on to a column of alumina (7x32 cm), previously deactivated with 10% acetic acid [hereinafter referred to as Column (l)] and eluted with the same solvent mixture.
The compositions of the following fractions (collected from Column (I)) are identified by paper chromatography using Whatman No. 1 paper [Registered Trade Mark] and the aforementioned benzene-chloroform mixture.
Column (I). Fraction: (a) a pigment; (b) a substance of Rf 0.66; (c) a small quantity of a substance of Rf 0.66 and a substance of Rf 0.45; (d) a substance of Rf 0.45.
Fraction (c) is obtained from the column and concentrated. The solid residue is dissolved in the aforementioned benzene-chloroform mixture (15 ml) and fractionated further on a second deactivated alumina column (4x30cm). From this column [hereinafter referred to as Column (II)] the following fractions are collected and identified using the same chromatographic system as was used for identifying the fractions of Column (I).
Column (II). Fraction: (a) a substance of Rf 0.66; (b) a trace of a substance of Rf 0.66; (c) a substance of Rf 0.45.
The fractions (d) of Column (I) and (c) of Column (II) are combined and evaporated and the residue (80 g) crystallized from methanol and ether followed by further re-crystallization from dilute alcohol. On heating to 120°C under a pressure of 0.01 mm/Hg, the crystals Iost water to give a compound, cymarin, which has an [α]d 22 =+39.0°. The [α]d 20 of cymarin (obtained from another source) in methanol is + 39.3°.
Alternatively, fractional crystallization may be used in place of adsorption chromatography
Cumarin may be also prepared from seeds of Strophantus Kombe

Therapeutic Function

Cardiotonic

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Biochem/physiol Actions

Cymarin is a cardiac glycoside and is classified as cardiotonic steroid. It inhibits ion transport by decreasing the activity of (Na-K)-ATPase.

CYMARIN Preparation Products And Raw materials

Raw materials

Preparation Products

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CYMARIN Suppliers

Specs
Tel
--
Fax
--
Email
info@specs.net
Country
The Netherlands
ProdList
6833
Advantage
70
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View Lastest Price from CYMARIN manufacturers

Career Henan Chemical Co
Product
cymarin 508-77-0
Price
US $1.00/KG
Min. Order
1g
Purity
99%
Supply Ability
100KG
Release date
2018-12-25

508-77-0, CYMARINRelated Search:


  • CIMARIN
  • CYMARIN
  • CYMARINE
  • 3β-[(3-O-Methyl-2,6-dideoxy-β-D-ribo-hexopyranosyl)oxy]-5,14-dihydroxy-19-oxo-5β-card-20(22)-enolide
  • WV-90043a
  • 20(22),5BETA-CARDENOLID-19-AL-3BETA,5BETA,14BETA-TRIOL 3BETA-MIXED GLYCOSIDES
  • K STROPHANTHIN
  • K-STROPHANTHIN-A
  • K-STROPHANTHIN-ALPHA
  • K-STROPHANTHIDIN-D-CYMAROSIDE
  • KOMBETIN
  • STROPHANTHIN K
  • 3β-[(2,6-Dideoxy-3-O-methyl-β-D-ribo-hexopyranosyl)oxy]-5,14-dihydroxy-19-oxo-5β,14β-card-20(22)-enolide
  • 5-beta-card-20(22)-enolide,3-beta-(beta-d-cymarosyloxy)-5,14-dihydroxy-19-ox
  • alvonalmr
  • strofantidinacimaroside
  • (3beta,5beta)-3-[(2,6-dideoxy-4-O-beta-D\-glucopyranosyl-3-O-methyl-beta-D\-ribo-hexopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide
  • CYMARIN CRYSTALLINE
  • CYMARIN(P)
  • CYMARIN: TECH., 90%
  • Card-20(22)-enolide, 3-[(2,6-dideoxy-3-O-methyl-β-D-ribo-hexopyranosyl)oxy]-5,14-dihydroxy-19-oxo-, (3β,5β)-
  • CYMARIN USP/EP/BP
  • 508-77-0
  • Conjugates
  • Lipids
  • Sterols
  • Biochemicals and Reagents
  • BioChemical
  • Cardioglycosides & Glycosides
  • Carbohydrates
  • Carbohydrates A to
  • Carbohydrates P-ZBiochemicals and Reagents
  • Polysaccharide