Dioxane - Standard for GC, ≥99.7%(GC) , CAS No.123-91-1

CAS: 123-91-1 Cat. No.: D116156 Formule: C4H8O2 Poids moléculaire: 88.11 Beilstein Registry Number: 102551 Numéro CE: 204-661-8
DISPONIBLE À COMMANDE
GRADE & PURITY Standard for GC ? GC reference standard — characterized compound for calibrating GC methods. Use to build calibration curves and verify GC quantitation. ≥99.7%(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
★
Size
Allemagne (EU)
USA*
Price
Qty
5ml
D116156-5ml
3 En stock
6 En stock

12,06€

16,40€
Enregistrer 4,34 € (26.46%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

Standard for GC, ≥99.7%(GC) Standard for GC 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

Synonymes
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
Spécifications et pureté
Standard for GC, ≥99.7%(GC)
Conditions de stockage de stockage
Room temperature,Desiccated
Expédié en
FedEx DG Service
Grade
Standard for GC
Pureté
≥99.7%(GC)
Noms et identifiants
Pubchem Sid
Sourires canoniques
C1COCCO1
IUPAC Name
1,4-dioxane
InChIKey
RYHBNJHYFVUHQT-UHFFFAOYSA-N
INCHI
1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2
Isomères SMILES
C1COCCO1
WGK Allemagne
2
RTECS
JG8225000
Numéro ONU
1165
Groupe d'emballage
II
Poids moléculaire
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
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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

16 results found

Lot NumberCertificate TypeDateArticle
G2624200Certificate of AnalysisJul 29, 2026 D116156
D2610235Certificate of AnalysisApr 21, 2026 D116156
L2524279Certificate of AnalysisJan 05, 2026 D116156
A2403189Certificate of AnalysisOct 13, 2025 D116156
H2513542Certificate of AnalysisAug 18, 2025 D116156
D2501277Certificate of AnalysisApr 15, 2025 D116156
B2517296Certificate of AnalysisFeb 22, 2025 D116156
D2416224Certificate of AnalysisApr 19, 2024 D116156
C2415046Certificate of AnalysisMar 27, 2024 D116156
J2326283Certificate of AnalysisNov 03, 2023 D116156
F2308954Certificate of AnalysisJun 19, 2023 D116156
L2209301Certificate of AnalysisDec 15, 2022 D116156
K2204403Certificate of AnalysisNov 07, 2022 D116156
H2219267Certificate of AnalysisAug 30, 2022 D116156
E2224203Certificate of AnalysisJun 01, 2022 D116156
C2221052Certificate of AnalysisMay 31, 2022 D116156
Propriétés chimiques et physiques
SensibilitéHygroscopic.
Point de congélation (°C)11 °C
Indice de réfraction1.4175
Point d'éclair (°F)51.8 °F - closed cup
Point d'éclair (°C)11℃ - closed cup
Point d'ébullition (°C)101.1°C
Point de fusion (°C)11.8°C
Poids moléculaire88.110 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
FAQ et articles
How to Choose the Correct Reference Material Quality Grade?
Standard for GC: A Practical Guide
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
Calculateurs de solution
Avis

Avis des clients

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.