Stearic acid - Moligand™, ≥98.5%(GC), Grade I , CAS No.57-11-4

CAS: 57-11-4 Cat. No.: S754992 Fórmula: C18H36O2 Peso molecular: 284.48 Beilstein Registry Number: 608585 Número EC: 200-313-4 PubChem CID: 5281
Disponible para pedir
CALIDAD & PUREZA Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98.5%(GC) Grade I
Storage
Store at 2-8°C
Shipped In
Wet ice
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
1g
S754992-1g
Fabricado bajo pedido · 8–12 semanas
39,90US$
5g
S754992-5g
Fabricado bajo pedido · 8–12 semanas
122,90US$
25g
S754992-25g
Fabricado bajo pedido · 8–12 semanas
478,90US$
100g
S754992-100g
Fabricado bajo pedido · 8–12 semanas
976,90US$
Enter a quantity for the sizes you want to add.
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Por qué esta calidad

Moligand™, ≥98.5%(GC), Grade I Moligand™ para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

🌡

Almacenamiento y envío

Store at 2-8°C Envío Wet ice. Consulte el COA específico del lote para conocer las especificaciones exactas.

📋

Documentos de calidad

SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.

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Prueba documental

Citado en 541 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Descripción general

Stearic acid is a C18 saturated fatty acid.
Application:
Stearic acid has been used in fatty acid preparations.

Especificaciones

Especificaciones y pureza
Moligand™, ≥98.5%(GC), Grade I
Mecanismos bioquímicos y fisiológicos
β-stearic acid oxidation produces 8 molecules of FADH2 (flavin adenine dinucleotide) and NADH2 (nicotinamide adenine dinucleotide), as well as 9 molecules of acetyl-CoA.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Pureza
≥98.5%(GC)
Nombres e identificadores
Sonrisas canónicas
CCCCCCCCCCCCCCCCCC(=O)O
IUPAC Name
octadecanoic acid
InChIKey
QIQXTHQIDYTFRH-UHFFFAOYSA-N
INCHI
1S/C18H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3,(H,19,20)
Isómeros SMILES
CCCCCCCCCCCCCCCCCC(=O)O
WGK Alemania
1
RTECS
WI2800000
PubChem CID
5281
Peso molecular
284.48
Beilstein
608585
Reaxy-Rn
608585

Documentación

📋 Hoja de datos de seguridad (SDS)

Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.

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

✅ Certificado de análisis (COA)

Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.

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📊 Ficha técnica

Resumen de referencia rápida de las especificaciones y aplicaciones del producto.

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🔬 Hoja de especificaciones

Atributos de calidad completos y criterios de aceptación para esta calidad.

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Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClaseFatty Acyls
SubclassFatty acids and conjugates
Intermediate Tree Nodes Not available
Direct ParentLong-chain fatty acids
Alternative Parents Straight chain fatty acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Long-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
DescripciónThis compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
External Descriptors Straight chain fatty acids
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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 NumberCertificate TypeFechaArticulo
I2602002I2602002Certificate of AnalysisSep 04, 2026 S754992
I2602003I2602003Certificate of AnalysisSep 04, 2026 S754992
I2602004I2602004Certificate of AnalysisSep 04, 2026 S754992
I2602005I2602005Certificate of AnalysisSep 04, 2026 S754992
Propiedades químicas y físicas
Solubilidadchloroform: 100 mg/mL, clear, colorless
Punto de inflamación (°F)235.4 °F
Punto de inflamación (°C)196 ℃
Punto de ebullición (°C)361℃
Punto de fusión (°C)69.6°C
Peso molecular284.500 g/mol
XLogP37.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count16
Exact Mass284.272 Da
Monoisotopic Mass284.272 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count20
Formal Charge0
Complexity202.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)
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The Preparation Logic of Nearly Monodisperse Colloidal Quantum Dots: Precursor Conversion, Nucleation–Growth Control, Surface Chemistry, and Process Control in Scale-Up
Liquid Polyisoprene: Material Characteristics, Application Directions, and Selection Considerations
Alkyd Resins: From Oil/Fatty-Acid-Modified Polyesters to Autoxidative Drying — Understanding Their Structure and Film-Formation Mechanism
Potassium Fatty Acid Soaps: Structure and Formulation Applications—Production Processes, Alkalinity, Foam Control, and Low-Foam Cleaning
What Is the Difference Between Triethanolamine and Diethanolamine: Understanding Their Formulation Functions, Application Differences, and Selection Logic from a Molecular-Structure Perspective
Why Can 6501 (Cocamide DEA) Stabilize Foam and Build Viscosity? Structural Mechanism, 1:1/1:1.5 Differences, and Application Selection
Differences, Functions, and Selection Guidelines for Sodium Hydroxide Flakes, Granules, Liquid Caustic Soda, and Caustic Soda in Household and Personal Care Product Manufacturing: The Functional and Application Logic of Sodium Hydroxide
Why Do Daily Chemical Products Become Opaque? Formation Mechanisms of Milky Turbidity, Pearlescence, and Coverage, and How to Select the Right Ingredients
From Structure to Selection: Mechanisms and Application Assessment of Low-Foam Oil and Wax Removal with Fatty Acid Methyl Ester Ethoxylates (FMEE)
Mechanism of Action and Selection Logic of Defoamers for Daily Chemical Products: Foam Stability, Foam-Breaking Mechanisms, and Representative Raw Material Analysis
Understanding Anionic Surfactants in Household and Personal-Care Formulations from a Structural Perspective: Structural and Performance Differences among Representative Raw Materials such as LAS, AES, K12, AOS, MES, and FMES
Analysis of Amino Acid-Based Surfactants: Basic Structure, Performance Origins, Category Selection, and Applications in Personal Care Formulations
Understanding Ceramides from the Perspective of the Stratum Corneum Lipid Barrier: Moisturizing and Barrier-Repair Mechanisms, Ingredient Selection, and Formulation Research Considerations
Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies
Antioxidant Mechanisms, Stability, and Delivery Strategies of Resveratrol in Skincare Research
Antioxidant Mechanisms of Ferulic Acid in Skincare, Vitamin C/E Synergy, and Stable Delivery Applications
The Moisturizing and Low-Moisture Protective Mechanisms of Trehalose: From Its α,α-1,1 Structure and Hydration Dynamics to In Vitro Skin Barrier Research
Protective and Potential Reparative Mechanisms of Prinsepia utilis Seed Oil on the Skin Barrier: Fatty Acid Composition, Epidermal Lipid Metabolism, and Research Evidence
UVA Absorption Mechanism of Avobenzone: Keto–Enol Tautomerism, Photochemical Instability, and Formulation Photostabilization Strategies
Structure, Stratum Corneum Distribution, and Stratum Corneum Conditioning Mechanism of Capryloyl Salicylic Acid: Barrier Effects and Safety Evaluation
Potential Mechanisms of Tea Polyphenols in Oily, Acne-Prone Skin: Effects of EGCG on Sebum Production, Lipid Peroxidation, and Inflammatory Responses
Structure and Functions of Fibronectin: Cell Adhesion, Cutaneous Wound Repair, and Topical Applications
Mechanisms by Which Fructan-Rich Ophiopogon japonicus Tuberous Root Extract Supports Skin Moisturization and Barrier Function
How Coenzyme Q10 Acts on the Skin: Mitochondrial Electron Transfer, Antioxidant Protection of Membrane Lipids, and Lipid-Carrier Delivery
What Is Direct Compression? Process Characteristics, Suitability Criteria, and Excipient Selection
How Ectoine Regulates Skin Hydration: Zwitterionic Structure, Preferential Hydration, and Barrier-Support Mechanisms
Are Lipids Fats? Understanding the Multiple Functions of Lipids from Cellular Metabolism to mRNA Delivery
Bakuchiol Is Not “Plant Retinol”: Chemical Structure, Anti-Aging Mechanisms, and Functional Similarities and Differences Compared with Retinol
Structure, Emollient and Moisturizing Effects, and Source Identification of Squalane: From Complete Hydrogenation of Squalene to Stable Isotope Analysis
Stratum Corneum Penetration and Skin Mechanisms of Panthenol: Moisturization, Barrier Repair, and Soothing Effects
Basis of Bisabolol’s Effects on Skin: Structure and Lipid Affinity, Inflammation Modulation, Antimicrobial Activity, and Percutaneous Penetration Enhancement
Citations of This Product
Calculadoras de soluciones
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