Dioxane - analytical standard, ≥99.9%(GC) , CAS No.123-91-1

CAS: 123-91-1 Cat. No.: D116162 Summenformel: C4H8O2 Molekulargewicht: 88.11 Beilstein Registry Number: 102551 EG-Nummer: 204-661-8
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GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. ≥99.9%(GC)
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
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Size
Deutschland (EU)
USA*
Price
Qty
5ml
D116162-5ml
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5 Auf Lager

51,98€

61,52€
Speichern 9,55 € (15.51%)
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Why this grade

analytical standard, ≥99.9%(GC) Analytischer Standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Desiccated 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.

📚

Literature proof

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

Specifications

Synonyme
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
Spezifikationen & Reinheit
analytical standard, ≥99.9%(GC)
Storage
Room temperature,Desiccated
Verschickt in
FedEx DG Service
Note
Analytischer Standard
Reinheit
≥99.9%(GC)
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
C1COCCO1
IUPAC Name
1,4-dioxane
InChIKey
RYHBNJHYFVUHQT-UHFFFAOYSA-N
INCHI
1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2
Isomere SMILES
C1COCCO1
WGK Deutschland
2
RTECS
JG8225000
UN-Nummer
1165
Verpackungsgruppe
II
Molekulargewicht
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
KlasseDioxanes
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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

5 results found

Lot NumberCertificate TypeDatumArtikel
L2425264Certificate of AnalysisSep 07, 2026 D116162
G2313253Certificate of AnalysisApr 09, 2025 D116162
J2109065Certificate of AnalysisJul 17, 2023 D116162
K2223270Certificate of AnalysisNov 14, 2022 D116162
A2108288Certificate of AnalysisOct 18, 2022 D116162
Chemische und physikalische Eigenschaften
EmpfindlichkeitHygroscopic.
Gefrierpunkt (°C)11 °C
Brechungsindex1.4175
Flammpunkt (°F)51.8 °F - closed cup
Flammpunkt (°C)11℃ - closed cup
Siedepunkt (°C)101.1°C
Schmelzpunkt (°C)11.8°C
Molekulargewicht88.110 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
FAQs und Artikel
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
Lösungsrechner
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