Morpholine - Standard for GC, ≥99.5%(GC) , CAS No.110-91-8

CAS: 110-91-8 Cat. No.: M109063 Fórmula: C4H9NO Peso molecular: 87.12 Beilstein Registry Number: 102549 Número EC: 203-815-1
Disponible para pedir
CALIDAD & PUREZA Standard for GC ? GC reference standard — characterized compound for calibrating GC methods. Use to build calibration curves and verify GC quantitation. ≥99.5%(GC)
Synonyms
Drewamine|Diethyleneimide oxide|Tetrahydro-1,4-isoxazine|Tetrahydro-1, 4-isoxazine|TETRAHYDRO-2H-1, 4-OXAZINE|Tetrahydro-4H-1-4-oxazine|Morpholine [UN2054] [Flammable liquid]|morpholin|4H-1,4-Oxazine, tetrahydro-|morphline|2H-1,4-Oxazine, tetrahydro-|Morpholine; Molsidomine Imp. E (EP); Molsidomine Impurity E|tetrahydro-14-iso-xazine|Tetryhydro-2H-1,4-oxazine|MORPHOLINE [IARC]|MORPHOLINE [FCC]|1-Oxa-4-azacyclohexane|DIEYTHYLENE OXIMIDE|Morpholine (BASF)|MORPHOLINE [MI]|1,4-oxazinane|MORPHOLINE-2,2,3,3,5,5,6,6-D8|Tetrahydro-p-oxazine|MORPHOLINE [INCI]|Tetrahydro-4H-1,4-Oxazine|Diethylene oximide|MORPHOLINE, PRACT|Morpholine [UN2054] [Flammable liquid]|Tetrahydro-1,4-oxazine|MORPHOLINE [HSDB]|MORPHOLINE|morpholine-|USEPA/OPP Pesticide Code: 054701|Morpholine on Rasta Resin|Tetrahydro-p-isoxazine|Diethylenimide oxide|BASF 238|morpho line|Morpholine purified by distillation from glass|p-Isoxazine, tetrahydro-|MORPHOLINE,REAG|Tetrahydro-2H-1,4-oxazine
Storage
Room temperature
Shipped In
FedEx DG Service
★
Talla
Alemania (EU)
USA*
Precio
Cantidad
5ml
M109063-5ml
—
4 Disponible

19,00€

21,61€
Guardar 2,60 € (12.05%)
Enter a quantity for the sizes you want to add.

Especificaciones

Sinónimos
Drewamine | Diethyleneimide oxide | Tetrahydro-1,4-isoxazine | Tetrahydro-1, 4-isoxazine | TETRAHYDRO-2H-1, 4-OXAZINE | Tetrahydro-4H-1-4-oxazine | Morpholine [UN2054] [Flammable liquid] | morpholin | 4H-1,4-Oxazine, tetrahydro- | morphline | 2H-1,4-Oxazine, tetrahydro- | Morpholine; Molsidomine Imp. E (EP); Molsidomine Impurity E | tetr Show more
Especificaciones y pureza
Standard for GC, ≥99.5%(GC)
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
FedEx DG Service
Grado
Standard for GC
Pureza
≥99.5%(GC)
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
C1COCCN1
IUPAC Name
morpholine
InChIKey
YNAVUWVOSKDBBP-UHFFFAOYSA-N
INCHI
1S/C4H9NO/c1-3-6-4-2-5-1/h5H,1-4H2
Isómeros SMILES
C1COCCN1
WGK Alemania
1
RTECS
QD6475000
Número ONU
2054
Grupo de embalaje
I
Peso molecular
87.12
Beilstein
102549
Reaxy-Rn
102549
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102549&ln=

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseOxazinanes
SubclassMorpholines
Intermediate Tree Nodes Not available
Direct ParentMorpholines
Alternative Parents Oxacyclic compounds  Dialkylamines  Dialkyl ethers  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Morpholine - Oxacycle - Azacycle - Secondary amine - Ether - Secondary aliphatic amine - 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 morpholines - saturated organic heteromonocyclic parent
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
H2624508H2624508Certificate of AnalysisSep 01, 2026 M109063
C2116148C2116148Certificate of AnalysisJul 03, 2026 M109063
G2318913G2318913Certificate of AnalysisMay 13, 2025 M109063
F2303017F2303017Certificate of AnalysisMar 04, 2025 M109063
L2412611L2412611Certificate of AnalysisDec 19, 2024 M109063
E2207150E2207150Certificate of AnalysisFeb 22, 2024 M109063
A2125058A2125058Certificate of AnalysisNov 10, 2022 M109063
Propiedades químicas y físicas
SolubilidadIt is miscible with water and can be miscible with most organic solvents.
SensibilidadHygroscopic
Índice de refracción1.4548
Punto de inflamación (°F)87.8 °F
Punto de inflamación (°C)35℃
Punto de ebullición (°C)128.3°C
Punto de fusión (°C)-4.76°C
Peso molecular87.120 g/mol
XLogP3-0.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass87.0684 Da
Monoisotopic Mass87.0684 Da
Topological Polar Surface Area21.300 Ų
Heavy Atom Count6
Formal Charge0
Complexity34.500
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
Standard for GC: A Practical Guide
OSF/ASF Dual-Channel Toolbox: Divergent Reactions of Four-Membered Ring Sulfonyl Fluorides, Condition “Knobs,” and Selection Navigation
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)
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)
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
Application of Shellac, a Natural Film-Forming Resin, in Coatings: Alcohol-Soluble Fast-Drying Film Formation, Sealing and Repair, and Performance Boundaries
Rationale for Applying Spirocyclic Building Blocks in Drug Molecule Optimization: Three-Dimensionalization, Conformational Control, and Property Trade-offs
Medicinal Chemistry Value of Heteroatom-Containing Small-Ring Spirocycles: Classical Heterocycle Replacement and Three-Dimensional Exit Vector Remodeling
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
How to Select Morpholine Intermediates: From Connection Sites and Target Bond Types to Synthetic Route Design
1,8-Naphthyridine-Based Aldose Reductase Inhibitors: Scaffold Construction, In Vitro Inhibitory Activity, and Directions for Structural Optimization
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Why Do Drugs “Borrow Water” to Bind Proteins? Structural and Thermodynamic Basis of Hydrogen Bonds Mediated by Bound Water
From 459,000 Recorded Ring Systems to 3,902 Candidate Ring Systems: Selection Patterns of Clinically Relevant Ring Systems
Desaturative Amination for the Synthesis of Amino Heteroarenes: Carbonyl-Site Predefinition of the C–N Bond-Forming Position and Subsequent Desaturative Aromatization
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.