1,4-Dioxane - anhydrous, ≥99.8% , CAS No.123-91-1

CAS: 123-91-1 Cat. No.: D431640 Formula: C4H8O2 Peso molecolare: 88.11 Beilstein Registry Number: 102551 Numero EC: 204-661-8
Disponibile su ordine
GRADE & PURITY Anhydrous Grade ? Anhydrous grade — water removed and packaged dry for moisture-sensitive chemistry. Use in reactions where even trace water would interfere or quench. ≥99.8%
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
Shipped In
FedEx DG Service
★
Size
Germania (EU)
USA*
Price
Qty
2ml
D431640-2ml
—
4 Disponibile
22,47€
4×2ml
D431640-4×2ml
Su ordinazione · 8–12 settimane

68,46€

80,61€
Salva 12,15 € (15.07%)
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Why this grade

anhydrous, ≥99.8% Anhydrous Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature 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.

Panoramica

Application

ZerO 2 products are rigorously degassed with highly pure inert gas providing solvents and solutions (anhydrous if specified) with very low residual oxygen content.

Specifications

Sinonimi
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
Specifiche e purezza
anhydrous, ≥99.8%
Condizioni di conservazione di stoccaggio
Room temperature
Spedito in
FedEx DG Service
Grado
Anhydrous Grade
Purezza
≥99.8%
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
C1COCCO1
IUPAC Name
1,4-dioxane
InChIKey
RYHBNJHYFVUHQT-UHFFFAOYSA-N
INCHI
1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2
Isomeri SMILES
C1COCCO1
WGK Germania
2
RTECS
JG8225000
Numero UN
1165
Gruppo di imballaggio
II
Peso molecolare
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=

Documentazione

📋 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
ClasseDioxanes
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
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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.

4 results found

Lot NumberCertificate TypeDataOggetto
A2515474Certificate of AnalysisJan 23, 2025 D431640
H2406422Certificate of AnalysisAug 12, 2024 D431640
G2409253Certificate of AnalysisJul 15, 2024 D431640
G2409254Certificate of AnalysisJul 15, 2024 D431640
Proprietà chimiche e fisiche
Punto di congelamento (°C)11 °C
Indice di rifrazione1.4175
Punto di infiammabilità (°F)51.8 °F - closed cup
Punto di infiammabilità (°C)11℃ - closed cup
Punto di ebollizione (°C)101.1°C
Punto di fusione (°C)11.8°C
Peso molecolare88.110 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
Domande frequenti e articoli
The Guide to Anhydrous Grade for Reagents
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
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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