Triethylamine - Anhydrous Grade, ≥99.5%, Water≤50 ppm , CAS No.121-44-8

CAS: 121-44-8 Cat. No.: T140677 Fórmula: C6H15N Peso molecular: 101.19 Beilstein Registry Number: 605283 Número EC: 204-469-4
Disponible para pedir
CALIDAD & PUREZA Anhydrous Grade ? Anhydrous grade — water removed and packaged dry for moisture-sensitive chemistry. Use in reactions where even trace water would interfere or quench. ≥99.5% Water≤50 ppm
Synonyms
triethyl amin | Triethylamine, for protein sequence analysis, ampule, >=99.5% (GC) | Triethylamine, United States Pharmacopeia (USP) Reference Standard | EINECS 204-469-4 | N,N-Diethylethanamine | N,N-diethyl-ethanamine | triehyl amine | TRIETHYLAMINE [MI
Storage
Protected from light,Room temperature,Argon charged
Shipped In
FedEx DG Service
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
100ml
T140677-100ml
5 Disponible
—

149,90US$

175,90US$
Guardar 26,00 US$ (14.78%)
500ml
T140677-500ml
3 Disponible
—

525,90US$

612,90US$
Guardar 87,00 US$ (14.19%)
Enter a quantity for the sizes you want to add.
🧪
Por qué esta calidad

Anhydrous Grade, ≥99.5%, Water≤50 ppm Anhydrous Grade para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

🌡

Almacenamiento y envío

Protected from light,Room temperature,Argon charged Envío FedEx DG Service. 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.

📚

Prueba documental

Citado en 2646 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Especificaciones

Sinónimos
triethyl amin | Triethylamine, for protein sequence analysis, ampule, >=99.5% (GC) | Triethylamine, United States Pharmacopeia (USP) Reference Standard | EINECS 204-469-4 | N,N-Diethylethanamine | N,N-diethyl-ethanamine | triehyl amine | TRIETHYLAMINE [MI
Especificaciones y pureza
Anhydrous Grade, ≥99.5%, Water≤50 ppm
Condiciones de almacenamiento de almacenamiento
Protected from light,Room temperature,Argon charged
Enviado en
FedEx DG Service
Grado
Anhydrous Grade
Pureza
≥99.5%
Nombres e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508811447
Sonrisas canónicas
CCN(CC)CC
IUPAC Name
N,N-diethylethanamine
InChIKey
ZMANZCXQSJIPKH-UHFFFAOYSA-N
INCHI
1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3
Isómeros SMILES
CCN(CC)CC
WGK Alemania
1
RTECS
YE0175000
Número ONU
1296
Grupo de embalaje
II
Peso molecular
101.19
Beilstein
605283

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.

Buscar COA →

📊 Ficha técnica

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

Ver ficha técnica →

🔬 Hoja de especificaciones

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

Ver hoja de especificaciones →

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClaseOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Tertiary amines
Direct ParentTrialkylamines
Alternative Parents Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen.
External Descriptors tertiary amine
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
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.

18 results found

Lot NumberCertificate TypeFechaArticulo
H2631512H2631512Certificate of AnalysisAug 25, 2026 T140677
H2631510H2631510Certificate of AnalysisAug 25, 2026 T140677
H2607062H2607062Certificate of AnalysisAug 12, 2026 T140677
G2228894G2228894Certificate of AnalysisMay 19, 2026 T140677
B2221022B2221022Certificate of AnalysisDec 10, 2025 T140677
F2509588F2509588Certificate of AnalysisApr 25, 2025 T140677
L2519070L2519070Certificate of AnalysisApr 25, 2025 T140677
F2509655F2509655Certificate of AnalysisApr 25, 2025 T140677
F2509587F2509587Certificate of AnalysisApr 25, 2025 T140677
C2330869C2330869Certificate of AnalysisNov 28, 2022 T140677
C2330871C2330871Certificate of AnalysisNov 28, 2022 T140677
C2330868C2330868Certificate of AnalysisNov 28, 2022 T140677
C2513185C2513185Certificate of AnalysisAug 31, 2022 T140677
G2228891G2228891Certificate of AnalysisAug 31, 2022 T140677
G2228895G2228895Certificate of AnalysisAug 31, 2022 T140677
B2221019B2221019Certificate of AnalysisMar 03, 2022 T140677
B2221021B2221021Certificate of AnalysisMar 03, 2022 T140677
B2221020B2221020Certificate of AnalysisMar 03, 2022 T140677
Propiedades químicas y físicas
SensibilidadAir sensitive, Light sensitive
Índice de refracción1.4003
Punto de inflamación (°F)12.2 °F
Punto de inflamación (°C)-11 °C
Punto de ebullición (°C)89~90°C
Punto de fusión (°C)-115°C
Peso molecular101.190 g/mol
XLogP31.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count3
Exact Mass101.12 Da
Monoisotopic Mass101.12 Da
Topological Polar Surface Area3.200 Ų
Heavy Atom Count7
Formal Charge0
Complexity25.700
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
Formaldehyde
Dimethyl sulfoxide (DMSO)
The Guide to Anhydrous Grade for Reagents
A Complete Guide to Ion-Pair Reversed-Phase Chromatography (IPC / IP-RP): Mechanisms, Four Tuning Knobs, Troubleshooting, and Ion-Pair Reagent Families (Tables 1–4)
Installing a Redox Switch on Biomolecules: Principles, Conjugation Essentials, and an Application Guide for ATTO MB2 NHS ester
OSF/ASF Dual-Channel Toolbox: Divergent Reactions of Four-Membered Ring Sulfonyl Fluorides, Condition “Knobs,” and Selection Navigation
Secondary Effects Behind Chromatographic Peak Tailing and Unstable Peak Shapes: How Residual Silanols (Si–OH) Affect Basic Compounds, and the Shortest Troubleshooting/Remediation Path (with Product Navigation and Tables 1–3)
Make “Aryl Chlorides + Low Pd Loading + Scale-Up Reproducibility” Reliable: The Initiation and Durability Logic of Pd–NHC (Palladium–N-Heterocyclic Carbene) Cross-Coupling (with Selection Navigation and Product Tables)
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
Understanding Cbz (Benzyloxycarbonyl): Selection Logic and Practical Value of a Classical Amino Protecting Group
Reconsidering N-Acyl Amino Protecting Groups: Deprotection Differences, Strategic Roles, and Experimental Selection of Ac, Bz, and Tfa
Selective Deprotection and Sulfonyl Group Migration of N-Aryl Sulfonamides Mediated by TfOH (Trifluoromethanesulfonic Acid): Reaction Patterns and Synthetic Implications
The Positioning of TBTU in Practice: Racemization Risk, Extended Uses, and Selection Criteria
The Methodological Value of Boc-Oxyma: Low-Racemization Coupling, Route Continuity, and Extended Applications
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
The Methodological Value of TPS-Cl: The Logic of Selective Activation and Representative Transformations in Nucleoside and Nucleotide Chemistry
The Methodological Value of TCFH: Advantages in Challenging Amidation and the Switching Logic of Carboxylic Acid Activation Pathways
Low-Racemization Control in Peptide Synthesis: An Inverse N→C Peptide Synthesis Strategy via Activated α-Aminoesters
Decision Logic for Selecting Coupling Reagents in Amide Bond Formation: Activation Pathways, Side Reactions, Epimerization, Workup, and Safety
Experimental Selection Logic for Carboxylic Acid Preactivation Pathways: Differences and Suitable Use Cases for Classical Mixed Anhydrides, CDI, Sulfonyl Chloride Systems, and the Yamaguchi System
Triphenylphosphine Dibromide (PPh₃Br₂) Is More Than Just a Brominating Reagent: Experimental Selection Logic from Alcohol-to-Alkyl Bromide Conversion to Carboxylic Acid Activation and One-Pot Esterification, Vinyl Bromide Formation, and Nitrile Constructi
Reaction Roles of DBU in Different Systems: Experimental Judgment from a Strong Organic Base to Nucleophilic Catalysis and Participation in the Reaction Pathway
Selection Logic for the Teoc Amino Protecting Group: From Fluoride-Triggered Deprotection to Orthogonal Protecting-Group Design
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization
Experimental Decision-Making for Introducing Aminoalkyl Side Chains Using N-Haloalkyl Phthalimides: Chain Length, Leaving Group, and Deprotection Choice
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
4-[(tert-Butyldimethylsilyl)oxy]butan-1-ol: Experimental Selection Logic as a Monoprotected 1,4-Butanediol Building Block and a Protected C4 Linker
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
Experimental Judgment for CMPI in Carboxylic Acid Activation: Applicable Tasks, Base Matching, and Workup Burden
Experimental Judgment for TFPN in Carboxylic Acid Activation: Suitable Scenarios, Intermediate Distribution, and Nucleophile Compatibility
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Adding a Temperature-Triggered Switch to NCO: How Blocked Isocyanates Affect the Storage, Curing, and Film Performance of 1K Baking Coatings
1K, 2K, Waterborne, Moisture-Curing, and Blocked Systems: Classification Logic and Identification Methods for Polyurethane Coating Curing Systems
Failure Mechanisms, Application Limitations, and Systematic Improvement Directions for Polyester Coatings
How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions
Polyurethane Coating Resins: Not a Single Resin, but a Designable High-Performance System
Application of Shellac, a Natural Film-Forming Resin, in Coatings: Alcohol-Soluble Fast-Drying Film Formation, Sealing and Repair, and Performance Boundaries
Cashew Nut Shell Liquid (CNSL): From Cashew Processing By-Product to Reactive Bio-Based Raw Material for Coating Resins
Waterborne Resin Technology Explained: Waterborne Forms, Performance Balance, and a Technology Map
Resin Polarity in Coating Formulations: From Molecular Structure to Dissolution, Compatibility, Interfacial Interactions, and Formulation Design
AITF-Mediated Carboxylic Acid Activation for the Synthesis of Amides, Peptides, and Esters: Activation Mechanism and Applicable Scenarios
Stabilization Design of Bridgehead α-Fluoroamines and Their Value as Medicinal Chemistry Building Blocks
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
Sulfonyl Hydrazide-Mediated Introduction of Small C(sp³) Fragments: Nickel-Catalyzed Cross-Coupling, Medicinal Chemistry Applications, and Reagent Selection
Medicinal Chemistry Design of the Indazole Scaffold: Tautomerism, Molecular Recognition, Substitution-Site Design, and Synthetic Strategies
Build the Three-Membered Ring First, or Form the Carbon–Nitrogen Bond First?—Retrosynthetic Strategies, Route Selection, and Stereochemical Control in Cyclopropylamine Synthesis
3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation
Activation of Carboxylic Acids by TFSP and Related Triflylpyridinium Reagents: Conversion to Aldehydes, Amides, Esters, and Oxazoles via Acylpyridinium Intermediates
Synthetic Route Design for Azaheterocyclic Phosphonates: Timing of C–P Bond Formation and Three Route Strategies
Supramolecular Materials: From Molecular Recognition and Self-Assembly to Dynamic Function
Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis
Citations of This Product
Calculadoras de soluciones
Reseñas

Reseñas de cliente

¿Quieres que te enviemos un mensaje cuando tengamos descuentos disponibles?

Recordármelo más tarde

¡Gracias! Por favor, revisa tu bandeja de entrada de correo electrónico para confirmar.

¡Vaya! Las notificaciones están desactivadas.