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Acetic acid - Suitable for inorganic trace analysis, ≥99% , CAS No.64-19-7

CAS: 64-19-7 Cat. No.: A433218 Formule: CH3CO2H Poids moléculaire: 60.05 Beilstein Registry Number: 506007 Numéro CE: 200-580-7
5269 Citations COA
Acetic acid - Suitable for inorganic trace analysis, ≥99% , CAS No.64-19-7
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Suitable for inorganic trace analysis ? Inorganic trace-analysis grade — minimal inorganic/metal contamination. Use when quantifying inorganic species at trace levels. ≥99%
Synonyms
Acetasol | Ethanoat | FEMA Number 2006 | HSDB 40 | Octowy kwas | Orthoacetic acid | Acetasol (TN) | Methanecarboxylic acid | 10.Methanecarboxylic acid | Acetic acid, ACS reagent, >=99.7% | Acido acetico [Italian] | HOOCCH3 | Acetic | Acido acetico | AI3-0
Storage
Room temperature
Shipped In
FedEx DG Service
★
Taille
USA
Allemagne (EU)*
Prix
Qté
250ml
A433218-250ml
Sur commande · 8–12 semaines

971,90$US

1 134,90$US
Enregistrer 163,00 $US (14.36%)
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SDS
Safety data
COA
Certificate
DS
Fiche technique
SP
Fiche de spécifications
Vue d’ensemble Spécifications Noms et identifiants Documentation Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis
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Pourquoi cette qualité

Suitable for inorganic trace analysis, ≥99% Suitable for inorganic trace analysis 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 Expédition FedEx DG Service. 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 5269 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Application

Omni Trace Ultra Product is double-distilled and packed in class 100 clean room conditions into preleached FEP bottles. Each FEP bottle is packed in an EPS innerpack and then packed into a 1x regulated carton with a Certificate of Analysis.

Spécifications

Synonymes
Acetasol | Ethanoat | FEMA Number 2006 | HSDB 40 | Octowy kwas | Orthoacetic acid | Acetasol (TN) | Methanecarboxylic acid | 10.Methanecarboxylic acid | Acetic acid, ACS reagent, >=99.7% | Acido acetico [Italian] | HOOCCH3 | Acetic | Acido acetico | AI3-0
Spécifications et pureté
Suitable for inorganic trace analysis, ≥99%
Conditions de stockage de stockage
Room temperature
Expédié en
FedEx DG Service
Grade
Suitable for inorganic trace analysis
Pureté
≥99%
Noms et identifiants
Sourires canoniques
CC(=O)O
IUPAC Name
acetic acid
InChIKey
QTBSBXVTEAMEQO-UHFFFAOYSA-N
INCHI
1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)
Isomères SMILES
CC(=O)O
WGK Allemagne
1
RTECS
AF1225000
Numéro ONU
2789
Groupe d'emballage
II
Poids moléculaire
60.05
Beilstein
506007
Reaxy-Rn
506007
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506007&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.

Voir la fiche de spécifications →

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  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monocarboxylic acid or derivatives - Carboxylic acid - 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 Straight chain fatty acids
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
FFAR2 Tchem Free fatty acid receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
FFAR3 Tchem Free fatty acid receptor 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
LCK Tclin Tyrosine-protein kinase LCK (9212 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FYN Tclin Tyrosine-protein kinase FYN (5308 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR2 Tchem Free fatty acid receptor 2 (545 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLL Tbio DNA polymerase lambda (184 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO2B1 Tchem Solute carrier organic anion transporter family member 2B1 (580 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
Caenorhabditis elegans (1055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meloidogyne incognita (862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Radish (446 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lolium rigidum (323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
Solubilité602.9g/L
Indice de réfraction1.37-1.373
Point d'éclair (°C)40℃
Point d'ébullition (°C)117-118°C
Point de fusion (°C)16-16.5°C
Poids moléculaire60.050 g/mol
XLogP3-0.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass60.0211 Da
Monoisotopic Mass60.0211 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count4
Formal Charge0
Complexity31.000
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
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Animal-Derived Collagen Recombinant Human Collagen Recombinant Humanized Collagen Triple Helix Immunogenicity Skin Repair Transepidermal Water Loss
3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
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Unnatural amino acids conformational restriction molecular building block 3,3-spiro-α-proline spiro quaternary carbon multigram-scale synthesis
Stereoretentive Decarboxylative Amidation with Dioxazolones: A Two-Electron Rearrangement Mechanism for Stereochemical Transfer from Chiral Carboxylic Acids
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
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Dioxazolone Decarboxylative Amidation Decarboxylation coupling
Desaturative Amination for the Synthesis of Amino Heteroarenes: Carbonyl-Site Predefinition of the C–N Bond-Forming Position and Subsequent Desaturative Aromatization
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
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aminopyridines aminopyrroles aminofurans aminothiophenes
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
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Drugs Aryl C–N
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