Decanoic acid - Moligand™, Standard for GC, ≥99%(GC) , Agonist of GPR84, CAS No.334-48-5, Agonist of GPR84

Name: Decanoic acid - Moligand™, Standard for GC, ≥99%(GC) , Agonist of GPR84, CAS No.334-48-5, Agonist of GPR84
Brand: Aladdin Scientific
SKU: D109189
Availability: InStock

CAS: 334-48-5 Cat. No.: D109189 Summenformel: C₁₀H₂₀O₂ Molekulargewicht: 172.26 Beilstein Registry Number: 1754556 EG-Nummer: 206-376-4

174 Citations COA

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QUALITÄT & REINHEIT Moligand™ ? Standard for GC ? ≥99%(GC)

Synonyms

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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

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Warum diese Qualität

Moligand™, Standard for GC, ≥99%(GC) Moligand™,Standard for GC für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Room temperature Versand Normal. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

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

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Literaturbeleg

In 174 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Spezifikationen

Synonyme

Spezifikationen & Reinheit

Moligand™, Standard for GC, ≥99%(GC)

Biochemische und physiologische Mechanismen

Decanoic acid (Standard) is the analytical standard of Decanoic acid. This product is intended for research and analytical applications. Decanoic acid is a key component of the medium-chain triglyceride (MCT) found in coconut oil. Decanoic acid is a brain

Storage

Room temperature

Verschickt in

Normal

Note

Moligand™, Standard for GC

Aktionsart

AGONIST

Mechanismus der Wirkung

Agonist of GPR84

Reinheit

≥99%(GC)

Namen und Kennungen

Pubchem Sid

508813841

Kanonisches Lächeln

CCCCCCCCCC(=O)O

IUPAC Name

decanoic acid

InChIKey

GHVNFZFCNZKVNT-UHFFFAOYSA-N

INCHI

1S/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12)

Isomere SMILES

CCCCCCCCCC(=O)O

WGK Deutschland

RTECS

HD9100000

Molekulargewicht

172.26

Beilstein

1754556

Reaxy-Rn

1754556

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1754556&ln=

Dokumentation

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Klasse Fatty Acyls
    - Subclass Fatty acids and conjugates

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Klasse	Fatty Acyls
Subclass	Fatty acids and conjugates
Intermediate Tree Nodes	Not available
Direct Parent	Medium-chain fatty acids
Alternative Parents	Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Medium-chain fatty acid - Straight chain fatty acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
External Descriptors	Straight chain fatty acids
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)

GPR84 Tchem G-protein coupled receptor 84 (0 Activities)

Discover Target: GPR84

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

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

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

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

ACHE Tclin Acetylcholinesterase (18204 Activities)

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

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

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

PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)

Discover Target: PPARA

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

HepG2 (196354 Activities)

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

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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

UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)

Discover Target: UGT1A8

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

UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)

Discover Target: UGT1A10

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

MONO-MAC-6 (495 Activities)

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

UGT1A3 Tbio UDP-glucuronosyltransferase 1-3 (217 Activities)

Discover Target: UGT1A3

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

Zugehörige Ziele (nicht menschlich)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

Discover Target: Ppard

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

Echinochloa crus-galli (3685 Activities)

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

Staphylococcus aureus (210822 Activities)

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

Bacillus subtilis (32866 Activities)

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

Meloidogyne incognita (862 Activities)

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

BCHE Cholinesterase (8742 Activities)

Discover Target: BCHE

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

Bursaphelenchus xylophilus (372 Activities)

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

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

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.

4 results found

Lot Number	Certificate Type	Datum	Artikel
E2508208	Certificate of Analysis	Oct 13, 2026	D109189
C2302415	Certificate of Analysis	Sep 03, 2026	D109189
D2523025	Certificate of Analysis	Apr 30, 2025	D109189
A2016012	Certificate of Analysis	Sep 06, 2023	D109189

Chemische und physikalische Eigenschaften

Gefrierpunkt (°C)	30 °C
Brechungsindex	1.4169
Flammpunkt (°F)	296.6 °F
Flammpunkt (°C)	147 °C
Siedepunkt (°C)	270°C
Schmelzpunkt (°C)	31.5°C
Molekulargewicht	172.260 g/mol
XLogP3	4.100
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	8
Exact Mass	172.146 Da
Monoisotopic Mass	172.146 Da
Topological Polar Surface Area	37.300 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	110.000
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

FAQs und Artikel

Standard for GC: A Practical Guide

Categories: Reagent Specifications, Grading and Purity

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Grade Standard for GC

Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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Fatty acids Long-chain carbon compounds

Potassium Fatty Acid Soaps: Structure and Formulation Applications—Production Processes, Alkalinity, Foam Control, and Low-Foam Cleaning

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Potassium salt Potassium fatty acid salt

Why Can 6501 (Cocamide DEA) Stabilize Foam and Build Viscosity? Structural Mechanism, 1:1/1:1.5 Differences, and Application Selection

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Non-ionic surfactants 6501 Cocamide DEA CDEA Coconut fatty acid diethanolamide

Zinc–Bismuth Composite Catalysts for Polyurethane: Cure Control, Selection Methods, and Blend-Ratio Design

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Catalysts Polyurethane

Citations of This Product

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Lösungsrechner

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📚 Zitationen nach Anwendung

Extraction & workup solvent106

Organic synthesis — reaction medium89

Other applications62

Chromatography (HPLC / GC / TLC)40

Cell viability1

Drug / compound screening5

Industrial & non-pharma application11

Controlled-release & nanoparticle carrier8

Topical & ophthalmic formulation4

Crystallization & recrystallization4

Spectroscopy sample preparation6

Electrochemistry & battery electrolyte5

Polymer synthesis & polymerization3

Cross-coupling reactions1

Nanoparticle / material biocompatibility1

Cell proliferation1

Alle 174 Zitationen ansehen →

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Decanoic acid - Moligand™, Standard for GC, ≥99%(GC) , Agonist of GPR84, CAS No.334-48-5, Agonist of GPR84

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Decanoic acid - Moligand™, Standard for GC, ≥99%(GC) , Agonist of GPR84, CAS No.334-48-5, Agonist of GPR84

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