Ammonium acetate solution - pharmaceutical grade, PharmPure™, for IVD application , CAS No.631-61-8

CAS: 631-61-8 Cat. No.: A433169 Summenformel: C2H7NO2 Molekulargewicht: 77.08 Beilstein Registry Number: 4186741 EG-Nummer: 211-162-9
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GRADE & PURITY PharmPure™ ? PharmPure™ — Aladdin's line of biopharmaceutical raw and starting materials. Use for pharma manufacturing inputs needing high purity and documentation. for IVD application ? IVD grade — quality and documentation for in-vitro diagnostic products. Use as a component in diagnostic assays and kits. Pharmaceutical grade ? Pharmaceutical grade — purity and documentation suitable for drug applications. Use for API/excipient work requiring pharma-level quality and traceability.
Synonyms
ammonia acetate salt | AMMONIUM ACETICUM [HPUS] | NH4OAc | DTXSID5023873 | E 264 | UNII-RRE756S6Q2 | CH3CO2NH4 | Acetic acid, ammonium salt (1:1) | E264 | E-264 | USFZMSVCRYTOJT-UHFFFAOYSA-N | AMMONIUM ACETATE | ammonium acetate- | EINECS 211-162-9 | AMMO
Storage
Store at 2-8°C
Shipped In
Wet ice
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Size
Deutschland (EU)
USA*
Price
Qty
500ml
A433169-500ml
—
1 Auf Lager
173,46€
Enter a quantity for the sizes you want to add.
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Why this grade

pharmaceutical grade, PharmPure™, for IVD application for IVD application,Pharmazeutische Qualität,PharmPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 735 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

5M Ammonium Acetate in Water. Solution is 0.2 μm filtered.Working solution 2.5M to be prepared by dilution with 200 proof Ethanol.

Application

For Precipitation of DNA and RNA, use 5 M Ammonium Acetate stock soluion to bring the final concentration of ammonium acetate in the working solution to 2.5 M.

Specifications

Synonyme
ammonia acetate salt | AMMONIUM ACETICUM [HPUS] | NH4OAc | DTXSID5023873 | E 264 | UNII-RRE756S6Q2 | CH3CO2NH4 | Acetic acid, ammonium salt (1:1) | E264 | E-264 | USFZMSVCRYTOJT-UHFFFAOYSA-N | AMMONIUM ACETATE | ammonium acetate- | EINECS 211-162-9 | AMMO
Spezifikationen & Reinheit
pharmaceutical grade, PharmPure™, for IVD application
Storage
Store at 2-8°C
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
for IVD application, Pharmazeutische Qualität, PharmPure™
Namen und Kennungen
Pubchem Sid528769501
Kanonisches LächelnCC(=O)[O-].[NH4+]
IUPAC Nameazanium;acetate
InChIKeyUSFZMSVCRYTOJT-UHFFFAOYSA-N
INCHI1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
Isomere SMILES CC(=O)[O-].[NH4+]
WGK Deutschland 1
RTECS AF3675000
Molekulargewicht 77.08
Beilstein 4186741
Reaxy-Rn 10774525
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10774525&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
KlasseCarboxylic acids and derivatives
SubclassCarboxylic acids
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acids
Alternative Parents Monocarboxylic acids and derivatives  Organic oxides  Organic nitrogen compounds  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
External Descriptors ammonium salt - acetate salt
3D-Struktur
Interaktives chemisches Strukturmodell





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.

2 results found

Lot NumberCertificate TypeDatumArtikel
J2418432Certificate of AnalysisJul 30, 2026 A433169
J2418446Certificate of AnalysisJul 30, 2026 A433169
Chemische und physikalische Eigenschaften
Schmelzpunkt (°C)114°C
Molekulargewicht77.080 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass77.0477 Da
Monoisotopic Mass77.0477 Da
Topological Polar Surface Area41.100 Ų
Heavy Atom Count5
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 Count2
FAQs und Artikel
For IVD Application
General Principles of Antibody Labeling with NHS-Activated Esters, F/P Calculation, and Troubleshooting Guide
Small-Molecule Inhibitors: A Practical Guide for Research Selection — A Minimal Evidence Chain and Scenario-Based Validation Framework (Including a Selection Matrix, Case Cards, and Product Tables 1–4)
Secondary Effects Behind Chromatographic Peak Tailing and Unstable Peak Shapes: How Residual Silanols (Si–OH) Affect Basic Compounds, and the Shortest Troubleshooting/Remediation Path (with Product Navigation and Tables 1–3)
2-Methylpyridine–Borane (2-Picoline·BH₃) Reductive Amination Guide: Process Drivers for Replacing NaBH₃CN, the Practical Operating Window, and Scale-Up/Quench Close-Out Essentials (Including Product Tables 1–3)
Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics
Ferulic Acid: Structural Features, Preparation Routes, and Key Points for Research Applications
Paeonol: Physicochemical Features, Uses, and Key Points for Research Applications
Famotidine: Physicochemical Features, Mechanism of Action, and Key Points for Research Applications
Roles of the Carboxypeptidase Family in Protein C-Terminal Processing and Experimental Analysis
Methodological Studies on Glycoprotein Structural Characterization and Quality Attribute Analysis
Research Framework for Multi-Enzyme Digestion Strategies and Optimization of Proteomic Coverage
Technical Comparison and Method Selection for Hydroxyproline Determination
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
Why Do Rust Spots Appear on Neutral Wall Putty? Iron Sources, Moisture Migration, Oxidative Color Development, and Prevention Measures
β-Hydroxybutyrate Detection Methods and Metabolic Significance: Comparative Applications of Enzymatic Assays, Blood Ketone Meters, and LC-MS
Principles, Method Comparison, and Sample Analysis Applications of Colorimetric Formaldehyde Detection
Citations of This Product
Lösungsrechner
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