N-Methyl morpholine - CP, ≥98% , CAS No.109-02-4

CAS: 109-02-4 Cat. No.: M104641 Peso molecular: 101.15 Beilstein Registry Number: 102719 Número EC: 203-640-0
Disponible para pedir
GRADE & PURITY CP ? Chemically Pure grade — moderate purity above technical grade but below analytical. Use for general lab reactions where ultra-low impurities aren't critical. ≥98%
Synonyms
4-Methylmorpholine, ReagentPlus(R), 99% | STL294217 | N-methyimorpholine | 4-methymorpholine | N-Methyl morphofine pound>>Morpholine, 4-methyl- | SCHEMBL4622 | 4-Methylmorpholine, BioXtra, suitable for protein sequencing, >=99.5% (GC) | N-methylmorphline
Storage
Protected from light,Room temperature
Shipped In
FedEx DG Service
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Size
Estado
Price
Qty
100ml
M104641-100ml
8

15,90US$

25,90US$
Guardar 10,00 US$ (38.61%)
500ml
M104641-500ml
≥10
37,90US$
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Why this grade

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

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Storage & shipping

Protected from light,Room temperature Ships FedEx DG Service 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 69 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
4-Methylmorpholine, ReagentPlus(R), 99% | STL294217 | N-methyimorpholine | 4-methymorpholine | N-Methyl morphofine pound>>Morpholine, 4-methyl- | SCHEMBL4622 | 4-Methylmorpholine, BioXtra, suitable for protein sequencing, >=99.5% (GC) | N-methylmorphline
Especificaciones y pureza
CP, ≥98%
Condiciones de almacenamiento de almacenamiento
Protected from light, Room temperature
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
CP
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488180631
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180631
Sonrisas canónicasCN1CCOCC1
IUPAC Name4-methylmorpholine
InChIKeySJRJJKPEHAURKC-UHFFFAOYSA-N
INCHI1S/C5H11NO/c1-6-2-4-7-5-3-6/h2-5H2,1H3
Isómeros SMILES CN1CCOCC1
WGK Alemania 1
RTECS QE5775000
Número ONU 2535
Grupo de embalaje II
Peso molecular 101.15
Beilstein 102719
Reaxy-Rn 102719
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102719&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ 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.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseOxazinanes
SubclassMorpholines
Intermediate Tree Nodes Not available
Direct ParentMorpholines
Alternative Parents Trialkylamines  Oxacyclic compounds  Dialkyl ethers  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Morpholine - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
External Descriptors Not available
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:

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18 results found

Lot NumberCertificate TypeFechaArticulo
D2602183Certificate of AnalysisApr 11, 2026 M104641
D2602182Certificate of AnalysisApr 11, 2026 M104641
A2612020Certificate of AnalysisJan 16, 2026 M104641
L2417282Certificate of AnalysisDec 27, 2024 M104641
L2417281Certificate of AnalysisDec 27, 2024 M104641
L2122532Certificate of AnalysisSep 21, 2023 M104641
L2122535Certificate of AnalysisSep 21, 2023 M104641
E2424040Certificate of AnalysisJul 28, 2023 M104641
G2321885Certificate of AnalysisJul 28, 2023 M104641
G2321886Certificate of AnalysisJul 28, 2023 M104641
J2418120Certificate of AnalysisJul 28, 2023 M104641
D23181229Certificate of AnalysisApr 21, 2023 M104641
D23181177Certificate of AnalysisApr 21, 2023 M104641
G2103014Certificate of AnalysisApr 12, 2023 M104641
A2306259Certificate of AnalysisJan 11, 2023 M104641
K2228284Certificate of AnalysisDec 01, 2022 M104641
L2009042Certificate of AnalysisSep 19, 2022 M104641
F2225388Certificate of AnalysisDec 27, 2021 M104641

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Propiedades químicas y físicas
SolubilidadMiscible with water, soluble in benzene.
SensibilidadLight sensitive.
Índice de refracción1.4332
Punto de inflamación (°C)12℃
Punto de ebullición (°C)111-114°C
Punto de fusión (°C)-65°C
Peso molecular101.150 g/mol
XLogP3-0.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass101.084 Da
Monoisotopic Mass101.084 Da
Topological Polar Surface Area12.500 Ų
Heavy Atom Count7
Formal Charge0
Complexity50.000
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
Picking CP Grade Reagents: Applications, Limits, and Upgrade Paths
Why Do So Many Molecules Incorporate an “Oxadiazole Ring”? A Stability-Oriented Design Guide from Structural Effects to Application Storylines (with Product Navigation Tables 1–3)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
A New Balance in Coupling Reagents: How DMT-TU Balances Reactivity, Racemization Control, and Thermal Hazard
The Positioning of TBTU in Practice: Racemization Risk, Extended Uses, and Selection Criteria
The Methodological Value of HATU in Difficult Couplings: Reactivity Advantages, Stereochemical Retention, and Condition Management
The Methodological Value of Boc-Oxyma: Low-Racemization Coupling, Route Continuity, and Extended Applications
Low Racemization in Peptide Synthesis Is Not Just About Reagent Choice: Stereochemical Risk During the Activation Stage and Practical Strategies for Experimental Control
The Methodological Value of TCFH: Advantages in Challenging Amidation and the Switching Logic of Carboxylic Acid Activation Pathways
Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression
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
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 Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Experimental Judgment for TFPN in Carboxylic Acid Activation: Suitable Scenarios, Intermediate Distribution, and Nucleophile Compatibility
Selective Acylation of Less Reactive Amines in Complex Substrates: Strategies for N/O and N/N Selectivity Control This article draws on the work of Li et al. on the TCFH/catalytic Oxyma system and transient imine protection, and summarizes design strateg
How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions
Peptide Intermediates Difficult to Dissolve and Separate? Route Design and Workup Strategies for Tag-Assisted Liquid-Phase Peptide Synthesis (TAG-LPPS)
Citations of This Product
Referencias
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