Name: Friedelin - ≥98% , CAS No.559-74-0
SKU: F331475
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Friedelin - ≥98% , CAS No.559-74-0

CAS: 559-74-0 Cat. No.: F331475 Summenformel: C₃₀H₅₀O Molekulargewicht: 426.72 Beilstein Registry Number: 1916451 EG-Nummer: 209-205-1

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GRADE & PURITY ≥98%

Synonyms

Storage

Vor Licht geschützt, bei -20°C lagern

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Eistruhe + Eispads

Übersicht Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Citations of This Product Lösungsrechner Bewertungen

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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Vor Licht geschützt, bei -20°C lagern Ships Eistruhe + Eispads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Friedelin ist ein Triterpen-Naturprodukt, das aus der Rinde der Korkeiche (Quercus suber) isoliert wurde. Friedelin ist das am häufigsten vorkommende Triterpen in Extrakten, die aus diesem Baum isoliert wurden. Friedelin wurde zusammen mit ähnlichen Triterpenen bei der Untersuchung von Inhibitoren der Photosynthese für die Verwendung als Herbizide beschrieben und hat antifungale und antimikrobielle Eigenschaften.

Anwendung des Produkts:

Friedelin ist der Hauptbestandteil der Triterpene in Korkextrakten

Specifications

Synonyme

Spezifikationen & Reinheit

≥98%

Storage

Vor Licht geschützt, bei -20°C lagern

Verschickt in

Eistruhe + Eispads

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

504756060

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504756060

Kanonisches Lächeln

CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C

IUPAC Name

(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one

InChIKey

OFMXGFHWLZPCFL-SVRPQWSVSA-N

INCHI

1S/C30H50O/c1-20-21(31)9-10-22-27(20,5)12-11-23-28(22,6)16-18-30(8)24-19-25(2,3)13-14-26(24,4)15-17-29(23,30)7/h20,22-24H,9-19H2,1-8H3/t20-,22+,23-,24+,26+,27+,28-,29+,30-/m0/s1

Isomere SMILES

C[C@H]1C(=O)CC[C@@H]2[C@@]1(CC[C@H]3[C@]2(CC[C@@]4([C@@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C)C)C)C)C

WGK Deutschland

Molekulargewicht

426.72

Beilstein

1916451

Reaxy-Rn

2063030

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2063030&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Klasse Prenol lipids
    - Subclass Triterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Klasse	Prenol lipids
Subclass	Triterpenoids
Intermediate Tree Nodes	Not available
Direct Parent	Triterpenoids
Alternative Parents	Cyclic ketones Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Triterpenoid - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.
External Descriptors	Hopanes
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)

ACHE Tclin Acetylcholinesterase (18204 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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HL-60 (67320 Activities)

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HT-29 (80576 Activities)

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MCF7 (126967 Activities)

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SK-OV-3 (52876 Activities)

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TK-10 (45540 Activities)

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UACC-62 (47335 Activities)

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A549 (127892 Activities)

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HepG2 (196354 Activities)

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NCI-H460 (60772 Activities)

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SF-268 (49410 Activities)

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GPBAR1 Tchem G-protein coupled bile acid receptor 1 (1723 Activities)

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

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)

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Zugehörige Ziele (nicht menschlich)

Nos2 Nitric oxide synthase, inducible (3573 Activities)

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Spinacia oleracea (250 Activities)

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Hepatitis B virus (7925 Activities)

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RAW264.7 (28094 Activities)

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BCHE Cholinesterase (8742 Activities)

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Phytophthora cactorum (113 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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.

7 results found

Lot Number	Certificate Type	Datum	Artikel
L2306215	Certificate of Analysis	Sep 01, 2026	F331475
L2306216	Certificate of Analysis	Sep 01, 2026	F331475
L2306217	Certificate of Analysis	Sep 01, 2026	F331475
L2306234	Certificate of Analysis	Sep 01, 2026	F331475
L2306235	Certificate of Analysis	Sep 01, 2026	F331475
L2306236	Certificate of Analysis	Sep 01, 2026	F331475
L2306237	Certificate of Analysis	Sep 01, 2026	F331475

Chemische und physikalische Eigenschaften

Löslichkeit	Soluble in water (partly), chloroform (1:8), and alcohol (1:250).
Empfindlichkeit	Moisture sensitive；light sensitive
Brechungsindex	n20D1.50 (Predicted)
Spezifische Drehung [α]	α20D-12°±3°, c = 1 in chloroform
Siedepunkt (°C)	~477.2° C at 760 mmHg (Predicted)
Schmelzpunkt (°C)	262-265° C (lit.)
Molekulargewicht	426.700 g/mol
XLogP3	9.800
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	426.386 Da
Monoisotopic Mass	426.386 Da
Topological Polar Surface Area	17.100 Å²
Heavy Atom Count	31
Formal Charge	0
Complexity	781.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	9
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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Lösungsrechner

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Bewertungen

📚 Citations by Application

Extraction & workup solvent1

Organic synthesis — reaction medium1

Drug / compound screening1

IC50 determination1

Cytotoxicity screening1

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Friedelin - ≥98% , CAS No.559-74-0

Storage & shipping

Quality documents

Literature proof

Übersicht

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

📚 Citations by Application

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