Aloe-emodin - ≥95% , CAS No.481-72-1

Name: Aloe-emodin - ≥95% , CAS No.481-72-1
SKU: A111278
Availability: InStock

CAS: 481-72-1 Cat. No.: A111278 Formula: C₁₅H₁₀O₅ Peso molecolare: 270.24 Beilstein Registry Number: 2059062 Numero EC: 207-571-7

24 Citations COA

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Disponibile su ordine

GRADE & PURITY ≥95%

Synonyms

9,10-Anthracenedione, 1,8-dihydroxy-3-(hydroxymethyl)- | Aloeemodin | Aloe-emodin | Aloe-emodin, analytical standard | Q-100526 | MLS000697563 | s2259 | CCG-208456 | SR-01000765772-3 | 3-(Hydroxymethyl)chrysazin | 9,10-Dihydro-4,5-dihydroxy-9,10-dioxo-2-h

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Size

Germania (EU)

USA*

Price

Qty

25mg

A111278-25mg

—

3 Disponibile

8,59€

12,93€
Salva 4,34 € (33.56%)

100mg

A111278-100mg

—

5 Disponibile

11,19€

17,27€
Salva 6,07 € (35.18%)

250mg

A111278-250mg

Su ordinazione · 8–12 settimane

12,93€

19,87€
Salva 6,94 € (34.93%)

500mg

A111278-500mg

—

2 Disponibile

16,40€

25,08€
Salva 8,68 € (34.60%)

A111278-1g

—

5 Disponibile

19,00€

28,55€
Salva 9,55 € (33.43%)

A111278-5g

Su ordinazione · 8–12 settimane

54,58€

82,35€
Salva 27,77 € (33.72%)

25g

A111278-25g

Su ordinazione · 8–12 settimane

163,92€

246,35€
Salva 82,44 € (33.46%)

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Panoramica Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni Domande frequenti

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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 24 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Aloe-emodin is a hydroxyanthraquinone and an active component present in Aloe vera leaves and root/rhizome of Rheum palmatum, possessing specific in vitro and in vivo antineuroectodermal tumor activity.

Specifications

Sinonimi

Specifiche e purezza

≥95%

Meccanismi biochimici e fisiologici

Laxative/cathartic compound; increases the contraction of intestinal smooth muscle by releasing endogenous acetylcholine. Anti-tumor activity is associated with an increased production of reactive oxygen species (ROS) that, in turn, reduces the mitochondr

Applicazione

Aloe-emodin may be used as a reference standard in the determination of aloe-emodin in Aloe vera extracts and commercial formulations using high-performance liquid chromatography (HPLC) coupled with tandem UV absorption and fluorimetric detection.

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Nota

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.

Purezza

≥95%

Nomi e identificatori

Pubchem Sid

488181089

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488181089

Sorrisi canonici

C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO

IUPAC Name

1,8-dihydroxy-3-(hydroxymethyl)anthracene-9,10-dione

InChIKey

YDQWDHRMZQUTBA-UHFFFAOYSA-N

INCHI

1S/C15H10O5/c16-6-7-4-9-13(11(18)5-7)15(20)12-8(14(9)19)2-1-3-10(12)17/h1-5,16-18H,6H2

Isomeri SMILES

C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO

WGK Germania

RTECS

CB6712200

Peso molecolare

270.24

Beilstein

2059062

Reaxy-Rn

2059062

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2059062&ln=

Documentazione

📋 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.

Look up COA →

📊 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 Benzenoids
  - Classe Anthracenes
    - Subclass Anthraquinones

Kingdom	Organic compounds
Superclass	Benzenoids
Classe	Anthracenes
Subclass	Anthraquinones
Intermediate Tree Nodes	Not available
Direct Parent	Anthraquinones
Alternative Parents	Aryl ketones 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Primary alcohols Organic oxides Hydrocarbon derivatives Aromatic alcohols
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Anthraquinone - 9,10-anthraquinone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Vinylogous acid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homopolycyclic compound
Descrizione	This compound belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.
External Descriptors	Anthracenes and phenanthrenes
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

Struttura 3D

Obiettivi associati (umani)

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

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

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

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

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

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

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

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

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

MAOB Tclin Monoamine oxidase B (8835 Activities)

Discover Target: MAOB

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

XDH Tclin Xanthine dehydrogenase (1038 Activities)

Discover Target: XDH

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

P2RY12 Tclin Purinergic receptor P2Y12 (2369 Activities)

Discover Target: P2RY12

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

ELANE Tclin Leukocyte elastase (8173 Activities)

Discover Target: ELANE

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

CTSG Tchem Cathepsin G (2304 Activities)

Discover Target: CTSG

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

EPHX2 Tchem Epoxide hydratase (3844 Activities)

Discover Target: EPHX2

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

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

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

ALPG Tchem Alkaline phosphatase placental-like (1197 Activities)

Discover Target: ALPG

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

PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)

Discover Target: PIN1

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

A498 (42825 Activities)

Lot Number	Certificate Type	Data	Oggetto
J2211620	Certificate of Analysis	Jul 03, 2026	A111278
E2607029	Certificate of Analysis	May 13, 2026	A111278
E2607075	Certificate of Analysis	May 12, 2026	A111278
E2607044	Certificate of Analysis	May 12, 2026	A111278
G2606025	Certificate of Analysis	May 11, 2026	A111278
E2607013	Certificate of Analysis	May 11, 2026	A111278
K2507126	Certificate of Analysis	Nov 15, 2025	A111278
K2110514	Certificate of Analysis	Aug 12, 2025	A111278
F2517015	Certificate of Analysis	Jul 02, 2025	A111278
A2608043	Certificate of Analysis	Nov 19, 2024	A111278
K2414100	Certificate of Analysis	Nov 19, 2024	A111278
D2424089	Certificate of Analysis	Mar 09, 2024	A111278
D2424088	Certificate of Analysis	Mar 09, 2024	A111278
H2401015	Certificate of Analysis	Feb 27, 2024	A111278
B2420036	Certificate of Analysis	Feb 27, 2024	A111278
J2211616	Certificate of Analysis	May 25, 2023	A111278
J2211634	Certificate of Analysis	May 25, 2023	A111278
J2211659	Certificate of Analysis	May 25, 2023	A111278
J2211676	Certificate of Analysis	May 25, 2023	A111278
E1921029	Certificate of Analysis	Mar 08, 2023	A111278
B2325258	Certificate of Analysis	Mar 02, 2023	A111278
B2325259	Certificate of Analysis	Mar 02, 2023	A111278
K1826043	Certificate of Analysis	Sep 16, 2022	A111278
J1819038	Certificate of Analysis	Aug 10, 2022	A111278
B2325257	Certificate of Analysis	Nov 17, 2021	A111278
K2110548	Certificate of Analysis	Nov 17, 2021	A111278

Sensibilità	Heat sensitive;Air sensitive
Punto di fusione (°C)	223-224°C
Peso molecolare	270.240 g/mol
XLogP3	1.800
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	1
Exact Mass	270.053 Da
Monoisotopic Mass	270.053 Da
Topological Polar Surface Area	94.800 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	420.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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

Aloe-emodin - ≥95% , CAS No.481-72-1

Storage & shipping

Quality documents

Literature proof

Panoramica

Specifications

Documentazione

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

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