Copper(II) acetate monohydrate - Basic-Grade Reagents, for Preparation, crystal , CAS No.6046-93-1

CAS: 6046-93-1 Cat. No.: C433063 Formule: C4H6CuO4·H2O Poids moléculaire: 199.65 Beilstein Registry Number: 3730548 Numéro CE: 611-978-9
DISPONIBLE À COMMANDE
GRADE & PURITY Basic-Grade Reagents ? Cost-effective basic-grade reagents for routine, non-critical use. Use as an economical workhorse where premium purity is unnecessary. for Preparation ? Preparation grade — suited to preparative isolation and sample preparation. Use when preparing or purifying material rather than final analysis. crystal
Synonyms
CUPRIC ACETATE MONOHYDRATE [MI] | FT-0624043 | J-520115 | copper (II) acetate mono hydrate | Copper (II) Acetate Monohydrate | 39J9V52S86 | copper acetate-monohydrate | AKOS015907686 | Copper(2+) acetate, monohydrate | Cupric acetate monohydrate | COPPER
Storage
Room temperature
Shipped In
Normal
★
Size
Allemagne (EU)
USA*
Price
Qty
500g
C433063-500g
1 En stock
En stock ≥10

198,63€

232,47€
Enregistrer 33,84 € (14.56%)
Enter a quantity for the sizes you want to add.
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Why this grade

Basic-Grade Reagents, for Preparation, crystal Basic-Grade Reagents,for Preparation for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 423 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes
CUPRIC ACETATE MONOHYDRATE [MI] | FT-0624043 | J-520115 | copper (II) acetate mono hydrate | Copper (II) Acetate Monohydrate | 39J9V52S86 | copper acetate-monohydrate | AKOS015907686 | Copper(2+) acetate, monohydrate | Cupric acetate monohydrate | COPPER
Spécifications et pureté
Basic-Grade Reagents, for Preparation, crystal
Conditions de stockage de stockage
Room temperature
Expédié en
Normal
Grade
Basic-Grade Reagents, for Preparation
Noms et identifiants
Pubchem Sid
Sourires canoniques
CC(=O)[O-].CC(=O)[O-].O.[Cu+2]
IUPAC Name
copper;diacetate;hydrate
InChIKey
NWFNSTOSIVLCJA-UHFFFAOYSA-L
INCHI
1S/2C2H4O2.Cu.H2O/c2*1-2(3)4;;/h2*1H3,(H,3,4);;1H2/q;;+2;/p-2
Isomères SMILES
CC(=O)[O-].CC(=O)[O-].O.[Cu+2]
WGK Allemagne
3
RTECS
AG3500000
Numéro ONU
3077
Groupe d'emballage
II
Poids moléculaire
199.65
Beilstein
3730548
Reaxy-Rn
3730548
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3730548&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
ClasseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid salts
Direct ParentAcetate salts
Alternative Parents Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Organic copper salts  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkNot available
Substituents Acetate salt - Organic transition metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic copper salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





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.

1 results found

Lot NumberCertificate TypeDateArticle
L2325177Certificate of AnalysisSep 22, 2026 C433063
Propriétés chimiques et physiques
Solubilité72g/L
Point de fusion (°C)240 °C
Poids moléculaire199.650 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass198.967 Da
Monoisotopic Mass198.967 Da
Topological Polar Surface Area81.300 Ų
Heavy Atom Count10
Formal Charge0
Complexity25.500
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 Count4
FAQ et articles
Dimethoxymethylsilane, DMMS
“For Preparation” Reagents Explained
Understanding Basic-Grade Reagents: The Cost-Effective Workhorse of the Lab
TEMPO-Catalyzed Oxidation Quick Reference (Alcohol Oxidation Focus): Three Regeneration Routes (NaOCl / Cu–O₂ / PIDA) + Selection & Troubleshooting
Transition-Metal Salts/Precursor Selection Guide: How “Different Salts of the Same Metal” Start from Different Chemical Realities—and How to Reproduce Results (including a Selection Navigator and Product Tables 1–5)
Experimental Selection Logic for C-C Bond Construction: Understanding Fragment Coupling, Carbonyl Chain Extension, Olefination, and Late-Stage Bond-Forming Pathways by Bond-Forming Task
Reaction Selection in Small-Molecule Synthesis: From Transformation-Type Assessment to Experimental Route Screening
Experimental Selection Logic for Transition-Metal-Catalyzed C–H Functionalization: When It Is Worth Pursuing and How to Assess Site Selectivity and Conditions
Copper Tripeptide GHK-Cu and Skin Repair: From Copper Coordination Chemistry to Extracellular Matrix Remodeling
Why Do Skincare Oligopeptides Have Different Effects? — Molecular Structure, Skin Delivery, and Mechanisms of Action
Citations of This Product
Calculateurs de solution
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