Cesium carbonate - purum p.a., ≥98%(T) , CAS No.534-17-8

CAS: 534-17-8 Cat. No.: C432848 Fórmula: Cs2CO3 Peso molecular: 325.82 Beilstein Registry Number: 4546405 Número CE: 208-591-9
Disponível para encomenda
GRADE & PURITY purum p.a. ? Purum pro analysi — pure grade meeting analytical specifications. Use for analytical applications where purum-level purity is validated for analysis. ≥98%(T)
Synonyms
cesiumcarbonate | cesium-carbonate | EC 208-591-9 | Cesium Carbonate(Powder) | DTXSID0052178 | Cesium carbonate, Cabot high-purity grade | Cesium carbonate, ReagentPlus(R), 99% | EINECS 249-784-8 | NSC-112218 | SY001250 | A829574 | caesium carbonat | MFCD
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Size
Alemanha (EU)
USA*
Price
Qty
10g
C432848-10g
—
3 Em stock

64,99€

76,27€
Gravar 11,28 € (14.79%)
50g
C432848-50g
—
2 Em stock

190,82€

223,79€
Gravar 32,97 € (14.73%)
250g
C432848-250g
Sob encomenda · 8–12 semanas

489,32€

571,75€
Gravar 82,44 € (14.42%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

purum p.a., ≥98%(T) purum p.a. for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal 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 783 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

Application

Catalyst for: aerobic oxidation of primary alcohols 1,4-addition reactions Reagent for: Synthesis of phosphazene derivatives Constrictive binding interactions Intramolecular C-N cross coupling reactions Dehydrohalogenative polycondensation Promotes the efficient O -alkylation of alcohols to form mixed alkyl carbonates.


Other Notes

Used for preparing cesium carboxylates which react with halogenides to give esters and lactones ; Used for an analogous preparation of thio ethers

Specifications

Sinónimos
cesiumcarbonate | cesium-carbonate | EC 208-591-9 | Cesium Carbonate(Powder) | DTXSID0052178 | Cesium carbonate, Cabot high-purity grade | Cesium carbonate, ReagentPlus(R), 99% | EINECS 249-784-8 | NSC-112218 | SY001250 | A829574 | caesium carbonat | MFCD
Especificações e pureza
purum p.a., ≥98%(T)
Condições de armazenamento de armazenamento
Room temperature,Argon charged
Enviado em
Normal
Grau
purum p.a.
Pureza
≥98%(T)
Nomes e identificadores
Pubchem Sid528774281
Sorrisos canónicosC(=O)([O-])[O-].[Cs+].[Cs+]
IUPAC Namedicesium;carbonate
InChIKeyFJDQFPXHSGXQBY-UHFFFAOYSA-L
INCHI1S/CH2O3.2Cs/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
SMILES isoméricas C(=O)([O-])[O-].[Cs+].[Cs+]
WGK Alemanha 2
RTECS FK9400000
Peso molecular 325.82
Beilstein 4546405
Reaxy-Rn 4546405
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4546405&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
SuperclassOrganic acids and derivatives
ClasseOrganic carbonic acids and derivatives
SubclassOrganic carbonic acids
Intermediate Tree Nodes Not available
Direct ParentOrganic carbonic acids
Alternative Parents Carbonate salts  Organic alkali metal salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Carbonate salt - Carbonic acid - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as organic carbonic acids. These are compounds comprising the carbonic acid functional group.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

3 results found

Lot NumberCertificate TypeDataItem
J2429176Certificate of AnalysisOct 31, 2024 C432848
J2429177Certificate of AnalysisOct 31, 2024 C432848
J2429178Certificate of AnalysisOct 31, 2024 C432848
Propriedades químicas e físicas
Ponto de fusão (°C)610°C
Peso molecular325.820 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass325.796 Da
Monoisotopic Mass325.796 Da
Topological Polar Surface Area63.200 Ų
Heavy Atom Count6
Formal Charge0
Complexity18.800
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 Count3
FAQs e artigos
Methanol
One-Stop Handbook for Palladium-Catalyzed Reactions: Catalytic Cycles, Deactivation Troubleshooting, Ligand/Precatalyst Selection, and an Aladdin Reference List
Strategies and Progress in the Asymmetric Catalytic Synthesis of Chiral 1,2-Bis(boronic) Esters: Route Types, Selectivity Challenges, and Sequential Site Utilization (with Product Selection Navigator and Tables 1–4)
Late-Stage Fluorination Toolbox: “Minimally Invasive Upgrades” for Lead Candidates: Four “Fluorine Knobs” → Two major routes (electrophilic vs nucleophilic) → An ¹⁸F-PET tracer branch → Selection navigation & representative product list
From Piperidine to Pyridine: The “Most Common N-Heterocycle” Shift in FDA Small-Molecule New Drugs (2013–2023) and a Selection Guide (Tables 1–4)
Light-Emitting Polymers (LEPs): A Practical Panorama - A Core PL/EL Mechanistic Framework, Material Family Map, and Structural “Design Knobs” (including Product Tables 1–4 and a selection guide)
Structural–Functional Analysis of the Methoxy Group (–OCH₃) in Approved Small-Molecule Drugs: Mechanisms, Evidence Chains, and Product-Selection Navigation (with Related Product Tables)
Selection of Common Research Salts: A Task Map for Alkali Metal Salts & Alkaline Earth Metal Salts (with Product Tables 1–6)
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)
Choosing Boron Sources to Make Reactions Robust: How Boronic Acids, Boronate Esters, BF₃K Salts, and MIDA Improve Suzuki–Miyaura Start-Up and Scale-Up Reproducibility (with Product Tables 1–5)
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)
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
The Preparation Logic of Nearly Monodisperse Colloidal Quantum Dots: Precursor Conversion, Nucleation–Growth Control, Surface Chemistry, and Process Control in Scale-Up
Ynamide Coupling Reagents: From Low-Epimerization Activation Pathways to More Practically Usable N→C Inverse Peptide Synthesis
Experimental Judgment for TFPN in Carboxylic Acid Activation: Suitable Scenarios, Intermediate Distribution, and Nucleophile Compatibility
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Experimental Selection Logic for Phase-Transfer Catalysts: Choosing Catalysts by Phase-State System, Source of Anionic Species, and Reaction Task
Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection
Deoxyfluorination of Hydroxyalkyl-Substituted Aryl/Alkenyl Boronates: C–F Bond Construction and C–B Bond Retention via a BF3K Intermediate
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
Where Does the Selectivity in Piperidine C–H Functionalization Come From? — Nitrogen Effects, Chair Conformations, and Four Classes of Key Intermediates
Overcoming the Electronic-Effect Limitations of Nucleophilic Aromatic Substitution in Fluoroarenes: Anion Activation, Concerted Substitution, and HF Capture by t-Bu-P4
What Grade Is Purum? From Grade Meaning and Specification Interpretation to Reagent Selection
Bond-Forming Reactions of N-Sulfinylamine and the Synthesis of S(VI) Functional Groups: Two-Electron Addition, Radical Addition, and Formal Cycloaddition
Citations of This Product
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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.