Ergosterol - ≥95% , CAS No.57-87-4

Name: Ergosterol - ≥95% , CAS No.57-87-4
Brand: Aladdin Scientific
SKU: E105721
Availability: InStock

CAS: 57-87-4 Cat. No.: E105721 Summenformel: C₂₈H₄₄O Molekulargewicht: 396.65 Beilstein Registry Number: 2338604 EG-Nummer: 200-352-7

19 Citations COA

Zum Ende der Bildgalerie springen

Ergosterol - ≥95% CAS No(57-87-4) by Aladdin Scientific

Zum Anfang der Bildgalerie springen

Zu bestellen verfügbar

QUALITÄT & REINHEIT ≥95%

Synonyms

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Übersicht Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

🧪

Warum diese Qualität

≥95% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

🌡

Lagerung & Versand

Protected from light,Store at -20°C,Argon charged Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

📋

Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

📚

Literaturbeleg

In 19 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Dihexadecyl phosphate (DHP) is a negatively charged lipid that is used for the formation of model membranes.

product description：

Ergosterol or provitamin D2 is a biological precursor of Vitamin D2. It is found predominantly in cell membranes of fungi and protists such as trypanosomes.

application：

Ergosterol has been used:

as a component of yeast cell monolayer models, to study the effects of steroidal and triterpenoid saponins on the monolayers

as a standard sample, to isolate and identify a fungal metabolite fraction containing ergosterol

as a component of the culture medium to isolate the CYP51RNAi phenotype of Trypanosoma brucei gambiense, to verify ergosterol biosynthesis

Spezifikationen

Synonyme

Spezifikationen & Reinheit

≥95%

Biochemische und physiologische Mechanismen

Ergosterol has a role in maintaining the integrity of the cell membrane and its fluidity. The sterol has anti-tumor and anti-inflammatory properties.

Storage

Protected from light,Store at -20°C,Argon charged

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥95%

Namen und Kennungen

Pubchem Sid

508817198

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508817198

Kanonisches Lächeln

CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C

IUPAC Name

(3S,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

InChIKey

DNVPQKQSNYMLRS-APGDWVJJSA-N

INCHI

1S/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-10,18-20,22,24-26,29H,11-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,26-,27-,28+/m0/s1

Isomere SMILES

C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC=C4[C@@]3(CC[C@@H](C4)O)C)C

WGK Deutschland

UN-Nummer

2811

Molekulargewicht

396.65

Beilstein

2338604

Reaxy-Rn

2224515

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2224515&ln=

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

Umfassendes Dokument zu Gefahren, Handhabung, Lagerung und Einhaltung regulatorischer Vorschriften.

<<<<<<< HEAD SDS herunterladen → ======= SDS herunterladen → >>>>>>> release248-p3

✅ Analysezertifikat (COA)

Chargenspezifische Qualitätsdaten. Geben Sie Ihre Chargennummer ein, um das genaue COA abzurufen.

COA nachschlagen →

📊 Datenblatt

Kurzübersicht über Produktspezifikationen und Anwendungen.

Datenblatt ansehen →

🔬 Spezifikationsblatt

Vollständige Qualitätsmerkmale und Akzeptanzkriterien für diese Qualität.

Spezifikationsblatt ansehen →

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Klasse Steroids and steroid derivatives
    - Subclass Ergostane steroids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Klasse	Steroids and steroid derivatives
Subclass	Ergostane steroids
Intermediate Tree Nodes	Not available
Direct Parent	Ergosterols and derivatives
Alternative Parents	3-hydroxy delta-7-steroids 3-beta-hydroxysteroids 3-beta-hydroxy delta-5-steroids Delta-7-steroids Delta-5-steroids Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Ergosterol-skeleton - 3-hydroxy-delta-5-steroid - 3-hydroxy-delta-7-steroid - 3-hydroxysteroid - Hydroxysteroid - 3-beta-hydroxy-delta-5-steroid - 3-beta-hydroxysteroid - Delta-7-steroid - Delta-5-steroid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Alcohol - Organooxygen compound - Hydrocarbon derivative - Aliphatic homopolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.
External Descriptors	Ergosterols and C24-methyl derivatives
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

3D-Struktur

Zugehörige Ziele (menschlich)

GAPDH Tchem Glyceraldehyde-3-phosphate dehydrogenase liver (1284 Activities)

Discover Target: GAPDH

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

COLO 205 (50209 Activities)

Lot Number	Certificate Type	Datum	Artikel
H2627350	Certificate of Analysis	Sep 05, 2026	E105721
H2627353	Certificate of Analysis	Sep 05, 2026	E105721
H2627355	Certificate of Analysis	Sep 05, 2026	E105721
C2522034	Certificate of Analysis	May 09, 2023	E105721
E2306195	Certificate of Analysis	May 09, 2023	E105721
E2306196	Certificate of Analysis	May 09, 2023	E105721
G2523083	Certificate of Analysis	May 09, 2023	E105721
G2610111	Certificate of Analysis	May 09, 2023	E105721
H2612047	Certificate of Analysis	May 09, 2023	E105721
I2510028	Certificate of Analysis	May 09, 2023	E105721
J2220196	Certificate of Analysis	Oct 26, 2022	E105721
J2220197	Certificate of Analysis	Oct 26, 2022	E105721
J2220199	Certificate of Analysis	Oct 26, 2022	E105721
J2220208	Certificate of Analysis	Oct 26, 2022	E105721

Löslichkeit	insoluble in DMSO; insoluble in EtOH; insoluble in H2O
Empfindlichkeit	Sensitive to humidity, heat, air, and light
Spezifische Drehung [α]	-112.5 ° (C=1, THF)
Siedepunkt (°C)	250°C
Schmelzpunkt (°C)	156-158°C
Molekulargewicht	396.600 g/mol
XLogP3	7.400
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	4
Exact Mass	396.339 Da
Monoisotopic Mass	396.339 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	29
Formal Charge	0
Complexity	712.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	8
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

Ergosterol - ≥95% , CAS No.57-87-4

Lagerung & Versand

Qualitätsdokumente

Literaturbeleg

Übersicht

Spezifikationen

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

✅ Analysezertifikat (COA)

📊 Datenblatt

🔬 Spezifikationsblatt

Erweiterte Daten

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

📚 Zitationen nach Anwendung

View related series