Dioxane - UltraPureChrom™, for HPLC, ≥99.5% , CAS No.123-91-1

CAS: 123-91-1 Cat. No.: D116159 Fórmula: C4H8O2 Peso molecular: 88.11 Beilstein Registry Number: 102551 Número EC: 204-661-8
Disponible para pedir
GRADE & PURITY UltraPureChrom™ ? UltraPureChrom™ — Aladdin's ultra-pure line for chromatography and spectroscopy. Use as a premium solvent/reagent where the lowest impurity background is required. for HPLC ? Suitable for HPLC — meets purity needs for liquid-chromatography use. Use for routine HPLC mobile phases and sample prep. ≥99.5%
Synonyms
1-4-dioxane | AMY33329 | Dioksan | Dioxane-1,4 | EINECS 204-661-8 | Dioxane 1.4 | Glycolethylenether | 1,4-Dioxane, for HPLC | 5-19-01-00016 (Beilstein Handbook Reference) | Dioxane | EC 204-661-8 | 1,4- dioxane | 1,4 -dioxane | 1-4 Dioxane | Dioxyethylen
Storage
Room temperature,Desiccated
Shipped In
FedEx DG Service
★
Size
USA
Alemania (EU)*
Price
Qty
100ml
D116159-100ml
7 Disponible
—
17,90US$
500ml
D116159-500ml
8 Disponible
2 Disponible
69,90US$
Enter a quantity for the sizes you want to add.
🧪
Why this grade

UltraPureChrom™, for HPLC, ≥99.5% for HPLC,UltraPureChrom™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated Ships FedEx DG Service Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 547 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
1-4-dioxane | AMY33329 | Dioksan | Dioxane-1,4 | EINECS 204-661-8 | Dioxane 1.4 | Glycolethylenether | 1,4-Dioxane, for HPLC | 5-19-01-00016 (Beilstein Handbook Reference) | Dioxane | EC 204-661-8 | 1,4- dioxane | 1,4 -dioxane | 1-4 Dioxane | Dioxyethylen
Especificaciones y pureza
UltraPureChrom™, for HPLC, ≥99.5%
Condiciones de almacenamiento de almacenamiento
Room temperature,Desiccated
Enviado en
FedEx DG Service
Grado
for HPLC, UltraPureChrom™
Pureza
≥99.5%
Nombres e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508807074
Sonrisas canónicas
C1COCCO1
IUPAC Name
1,4-dioxane
InChIKey
RYHBNJHYFVUHQT-UHFFFAOYSA-N
INCHI
1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2
Isómeros SMILES
C1COCCO1
WGK Alemania
2
RTECS
JG8225000
Número ONU
1165
Grupo de embalaje
II
Peso molecular
88.11
Beilstein
102551
Reaxy-Rn
102551
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102551&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ 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.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseDioxanes
Subclass1,4-dioxanes
Intermediate Tree Nodes Not available
Direct Parent1,4-dioxanes
Alternative Parents Oxacyclic compounds  Dialkyl ethers  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Para-dioxane - Oxacycle - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 1,4-dioxanes. These are organic compounds containing 1,4-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 4.
External Descriptors a small molecule
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.

77 results found

Lot NumberCertificate TypeFechaArticulo
G2624199Certificate of AnalysisJun 30, 2026 D116159
G2624198Certificate of AnalysisJun 30, 2026 D116159
G2624197Certificate of AnalysisJun 30, 2026 D116159
G2624195Certificate of AnalysisJun 30, 2026 D116159
D2610234Certificate of AnalysisMar 25, 2026 D116159
D2610233Certificate of AnalysisMar 25, 2026 D116159
D2610232Certificate of AnalysisMar 25, 2026 D116159
L2524280Certificate of AnalysisDec 17, 2025 D116159
L2524277Certificate of AnalysisDec 17, 2025 D116159
L2524279Certificate of AnalysisDec 17, 2025 D116159
L2524278Certificate of AnalysisDec 17, 2025 D116159
H2513537Certificate of AnalysisAug 06, 2025 D116159
H2513541Certificate of AnalysisAug 06, 2025 D116159
H2513543Certificate of AnalysisAug 06, 2025 D116159
H2513544Certificate of AnalysisAug 06, 2025 D116159
B2517301Certificate of AnalysisFeb 14, 2025 D116159
B2517300Certificate of AnalysisFeb 14, 2025 D116159
B2517297Certificate of AnalysisFeb 14, 2025 D116159
B2517298Certificate of AnalysisFeb 14, 2025 D116159
F2524263Certificate of AnalysisFeb 14, 2025 D116159
D2501626Certificate of AnalysisFeb 14, 2025 D116159
D2501278Certificate of AnalysisFeb 14, 2025 D116159
J2431309Certificate of AnalysisOct 25, 2024 D116159
B2513089Certificate of AnalysisOct 25, 2024 D116159
J2431308Certificate of AnalysisOct 25, 2024 D116159
J2431310Certificate of AnalysisOct 25, 2024 D116159
J2431311Certificate of AnalysisOct 25, 2024 D116159
B2508102Certificate of AnalysisOct 25, 2024 D116159
H2408482Certificate of AnalysisAug 02, 2024 D116159
H2408485Certificate of AnalysisAug 02, 2024 D116159
H2408484Certificate of AnalysisAug 02, 2024 D116159
H2408483Certificate of AnalysisAug 02, 2024 D116159
D2416227Certificate of AnalysisMar 27, 2024 D116159
D2416228Certificate of AnalysisMar 27, 2024 D116159
D2416226Certificate of AnalysisMar 27, 2024 D116159
D2416225Certificate of AnalysisMar 27, 2024 D116159
D2412168Certificate of AnalysisMar 27, 2024 D116159
C2415047Certificate of AnalysisFeb 28, 2024 D116159
C2415055Certificate of AnalysisFeb 28, 2024 D116159
C2415050Certificate of AnalysisFeb 28, 2024 D116159
C2415049Certificate of AnalysisFeb 28, 2024 D116159
C2415048Certificate of AnalysisFeb 28, 2024 D116159
A2403166Certificate of AnalysisDec 06, 2023 D116159
A2403167Certificate of AnalysisDec 06, 2023 D116159
A2403168Certificate of AnalysisDec 06, 2023 D116159
J2326287Certificate of AnalysisOct 19, 2023 D116159
J2326286Certificate of AnalysisOct 19, 2023 D116159
J2326285Certificate of AnalysisOct 19, 2023 D116159
J2326284Certificate of AnalysisOct 19, 2023 D116159
H2330288Certificate of AnalysisJun 30, 2023 D116159
H2330287Certificate of AnalysisJun 30, 2023 D116159
H2330286Certificate of AnalysisJun 30, 2023 D116159
H2330285Certificate of AnalysisJun 30, 2023 D116159
F2308958Certificate of AnalysisMay 13, 2023 D116159
F2308957Certificate of AnalysisMay 13, 2023 D116159
F2308956Certificate of AnalysisMay 13, 2023 D116159
F2308955Certificate of AnalysisMay 13, 2023 D116159
D2301142Certificate of AnalysisMar 24, 2023 D116159
D2301175Certificate of AnalysisMar 24, 2023 D116159
D2301176Certificate of AnalysisMar 24, 2023 D116159
D2301177Certificate of AnalysisMar 24, 2023 D116159
L2209488Certificate of AnalysisNov 25, 2022 D116159
L2209489Certificate of AnalysisNov 25, 2022 D116159
L2201005Certificate of AnalysisOct 31, 2022 D116159
K2204407Certificate of AnalysisOct 20, 2022 D116159
K2204404Certificate of AnalysisOct 20, 2022 D116159
K2204405Certificate of AnalysisOct 20, 2022 D116159
K2204406Certificate of AnalysisOct 20, 2022 D116159
H2219269Certificate of AnalysisAug 12, 2022 D116159
H2219270Certificate of AnalysisAug 12, 2022 D116159
H2219268Certificate of AnalysisAug 12, 2022 D116159
G2222382Certificate of AnalysisJul 29, 2022 D116159
E2206032Certificate of AnalysisFeb 14, 2022 D116159
E2206034Certificate of AnalysisFeb 14, 2022 D116159
E2206037Certificate of AnalysisFeb 14, 2022 D116159
E2206038Certificate of AnalysisFeb 14, 2022 D116159
A2213016Certificate of AnalysisFeb 10, 2022 D116159
Propiedades químicas y físicas
SensibilidadHygroscopic.
Punto de congelación (°C)11 °C
Índice de refracción1.4175
Punto de inflamación (°F)51.8 °F - closed cup
Punto de inflamación (°C)11℃ - closed cup
Punto de ebullición (°C)101.1°C
Punto de fusión (°C)11.8°C
Peso molecular88.110 g/mol
XLogP3-0.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass88.0524 Da
Monoisotopic Mass88.0524 Da
Topological Polar Surface Area18.500 Ų
Heavy Atom Count6
Formal Charge0
Complexity26.500
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
Acetone
1, 4-Dioxane
UltraPureChrom™: The Pinnacle of Purity for Chromatography
Introduction: “Suitable for HPLC” (HPLC Grade)
HPLC-Grade Solvents for High-Performance Liquid Chromatography: From Concept to Practice
One-Stop Handbook for Palladium-Catalyzed Reactions: Catalytic Cycles, Deactivation Troubleshooting, Ligand/Precatalyst Selection, and an Aladdin Reference List
How to Make the Suzuki–Miyaura Reaction Robust: Pinpoint the Bottleneck and Lock in a Reproducible Operating Window (with Selection Navigation and Product Tables 1–5)
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Experimental Judgment for Differential Deprotection of Double Boc and Related N-Boc Systems: Substrate Type, Site-Response Differences, and Initial Condition Selection
Experimental Assessment of Fmoc Introduction Routes: Impurity Profile Differences, Raw Material Carryover, and Quality Control
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
AES (Fatty Alcohol Polyoxyethylene Ether Sulfate) in Personal and Home-Care Cleansing Formulations: An Analysis of Structure, Performance, and Low-Temperature Flowability
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Overcoming the Electronic-Effect Limitations of Nucleophilic Aromatic Substitution in Fluoroarenes: Anion Activation, Concerted Substitution, and HF Capture by t-Bu-P4
1,8-Naphthyridine-Based Aldose Reductase Inhibitors: Scaffold Construction, In Vitro Inhibitory Activity, and Directions for Structural Optimization
Form Selection of 2,5-Dihydropyrrol-3-yl Boron Building Blocks: Functional Roles of Bpin and BF₃K in Coupling, Isolation, and Storage
Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Citations of This Product
Calculadoras de soluciones
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