Ammonium acetate - Suitable for molecular biology, ≥98%, used for A green analytical method for the simultaneous determination of 17 perfluoroalkyl substances (PFAS) in human serum and semen by ultra-performance liquid chromatography-tandem mass spectrome

CAS: 631-61-8 Cat. No.: A112058 Formule: C2H7NO2 Poids moléculaire: 77.08 Beilstein Registry Number: 4186741 Numéro CE: 211-162-9
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Suitable for molecular biology ? Molecular-biology grade — free of nucleases and contaminants that degrade DNA/RNA. Use in cloning, PCR, and nucleic-acid work needing clean reagents. ≥98%
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
Room temperature,Argon charged,Desiccated
Shipped In
Normal
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Taille
Allemagne (EU)
USA*
Prix
Qté
500g
A112058-500g
—
3 En stock

58,92€

69,33€
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Pourquoi cette qualité

Suitable for molecular biology, ≥98% Suitable for molecular biology pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Room temperature,Argon charged,Desiccated Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 748 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes
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
Spécifications et pureté
Suitable for molecular biology, ≥98%
Application
A green analytical method for the simultaneous determination of 17 perfluoroalkyl substances (PFAS) in human serum and semen by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).: This study highlights the use of ammonium aceta
Conditions de stockage de stockage
Room temperature,Argon charged,Desiccated
Expédié en
Normal
Grade
Suitable for molecular biology
Pureté
≥98%
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508811973
Sourires canoniques
CC(=O)[O-].[NH4+]
IUPAC Name
azanium;acetate
InChIKey
USFZMSVCRYTOJT-UHFFFAOYSA-N
INCHI
1S/C2H4O2.H3N/c1-2(3)4;/h1H3,(H,3,4);1H3
Isomères SMILES
CC(=O)[O-].[NH4+]
WGK Allemagne
1
RTECS
AF3675000
Poids moléculaire
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

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic 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
DescriptionThis 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
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:

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16 results found

Lot NumberCertificate TypeDateArticle
J2610049J2610049Certificate of AnalysisOct 12, 2026 A112058
J2610051J2610051Certificate of AnalysisOct 12, 2026 A112058
D2503254D2503254Certificate of AnalysisApr 15, 2025 A112058
E2410268E2410268Certificate of AnalysisApr 11, 2024 A112058
E2410269E2410269Certificate of AnalysisApr 11, 2024 A112058
K2324104K2324104Certificate of AnalysisNov 07, 2023 A112058
K2324390K2324390Certificate of AnalysisNov 07, 2023 A112058
H2310072H2310072Certificate of AnalysisJul 20, 2023 A112058
H2310073H2310073Certificate of AnalysisJul 20, 2023 A112058
H2324036H2324036Certificate of AnalysisJul 20, 2023 A112058
D2325295D2325295Certificate of AnalysisApr 14, 2023 A112058
D2325302D2325302Certificate of AnalysisApr 14, 2023 A112058
C2321929C2321929Certificate of AnalysisMar 08, 2023 A112058
C2321932C2321932Certificate of AnalysisMar 08, 2023 A112058
H2204368H2204368Certificate of AnalysisJul 07, 2022 A112058
H2204370H2204370Certificate of AnalysisJul 07, 2022 A112058
Propriétés chimiques et physiques
SensibilitéMoisture sensitive
Point de fusion (°C)114°C
Poids moléculaire77.080 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
FAQ et articles
Molecular Biology Grade
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
Ammonium Acetate: Properties, Uses & Lab Guide
Ammonium Acetate Protocol: Preparation & Lab Applications
Citations of This Product
Calculateurs de solution
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Produits apparentés

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Ammonium acetate - HPLC grade, ≥99%, used for Ammonium acetate can be used as a reactant as well as a catalyst in the synthesis of: 1,3-oxazine derivatives by three-component condensation reaction with 2-naphthol and aromatic aldehydes. Symmet
Tetrabutylammonium acetate(TBAA) - ≥97%, 1:2(Acetic acid) , CAS No.10534-59-5 (1:2AcOH)
Tetraethylammonium acetate tetrahydrate - ≥99% , CAS No.67533-12-4
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n-Propylammonium trifluoroacetate - ≥98% , CAS No.326602-11-3
2-Methoxyethylammonium trifluoroacetate - ≥98% , CAS No.205490-67-1
iso-Propylammonium trifluoroacetate - ≥98% , CAS No.326602-12-4
Diphenylammonium trifluoroacetate - ≥98% , CAS No.328530-93-4
Di-Methylammonium trifluoroacetate - ≥98% , CAS No.2840-17-7
Di-butylammonium trifluoroacetate - ≥98% , CAS No.334-41-8
Di-isopropylammonium trifluoroacetate - ≥98% , CAS No.64836-67-5
Ammonium acetate solution - Suitable for molecular biology, 7.5 M , CAS No.631-61-8
Ammonium acetate - Ph.Eur., Suitable for Analysis, ACS, Premium pure , CAS No.631-61-8
Ammonium acetate solution - pharmaceutical grade, PharmPure™, for IVD application , CAS No.631-61-8
Ammonium trifluoroacetate - ≥98% , CAS No.3336-58-1

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