Benzoic acid solution - analytical standard, 1.00mg/ml in ethanol-water , CAS No.65-85-0

CAS: 65-85-0 Cat. No.: B117658 Formule: C7H6O2 Poids moléculaire: 122.12 Beilstein Registry Number: 636131 Numéro CE: 200-618-2
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 1.00mg/ml in ethanol-water
Synonyms
Benzoic acid solution Benzoic Acid Zone Refined
Storage
Room temperature
Shipped In
Normal
★
Taille
USA
Allemagne (EU)*
Prix
Qté
5ml
B117658-5ml
Sur commande · 8–12 semaines

61,90$US

73,90$US
Enregistrer 12,00 $US (16.24%)
Enter a quantity for the sizes you want to add.
🧪
Pourquoi cette qualité

analytical standard, 1.00mg/ml in ethanol-water Analytical standard pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

🌡

Stockage & expédition

Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

📋

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.

📚

Preuve documentaire

Cité dans 844 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes
Benzoic acid solution Benzoic Acid Zone Refined
Spécifications et pureté
analytical standard, 1.00mg/ml in ethanol-water
Conditions de stockage de stockage
Room temperature
Expédié en
Normal
Grade
Analytical standard
Noms et identifiants
Isomères SMILES
C1=CC=C(C=C1)C(=O)O
WGK Allemagne
1
RTECS
DG0875000
Numéro ONU
UN 1268
Groupe d'emballage
I
Poids moléculaire
122.12
Beilstein
636131
Reaxy-Rn
636131
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636131&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.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

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

Voir la fiche de spécifications →

Données avancées

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.

2 results found

Lot NumberCertificate TypeDateArticle
L2110276L2110276Certificate of AnalysisJun 09, 2025 B117658
G1820073G1820073Certificate of AnalysisDec 12, 2023 B117658
Propriétés chimiques et physiques
SensibilitéMoisture sensitive.
Indice de réfraction1.504
Point d'ébullition (°C)249°C
Point de fusion (°C)121-125℃
FAQ et articles
How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
Triphenylphosphine Dibromide (PPh₃Br₂) Is More Than Just a Brominating Reagent: Experimental Selection Logic from Alcohol-to-Alkyl Bromide Conversion to Carboxylic Acid Activation and One-Pot Esterification, Vinyl Bromide Formation, and Nitrile Constructi
Reaction Roles of DBU in Different Systems: Experimental Judgment from a Strong Organic Base to Nucleophilic Catalysis and Participation in the Reaction Pathway
DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization
Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Enzymatic Hydroxylation Mechanism of Salicylate Conversion to Catechol
Alkyd Resins: From Oil/Fatty-Acid-Modified Polyesters to Autoxidative Drying — Understanding Their Structure and Film-Formation Mechanism
Phenolic-Modified Alkyd Resin: Performance Enhancement and Applications in Fast-Drying Industrial Coatings
Why Are Preservative Systems in Daily Chemical Products Effective? Common Types, Mechanisms of Action, and Factors Affecting Preservation Efficacy
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Tea Tree Oil in Skincare: From Chemical Composition and Anti-Acne Mechanisms to Evidence Evaluation and Safe Use
Structure, Stratum Corneum Distribution, and Stratum Corneum Conditioning Mechanism of Capryloyl Salicylic Acid: Barrier Effects and Safety Evaluation
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Storage Stability and Deoxyfluorination Reactivity of ImCl[H₂F₃]—Reactivity Modulation of the H₂F₃⁻ Fluoride Source and Substrate Activation by 2-Chloroimidazolium
Rotary-Evaporation-Assisted Reversible Dehydration Reactions: Reduced-Pressure Evaporation, Removal of Volatile Components, and Equilibrium Response
Citations of This Product
Calculateurs de solution
Avis

Avis des clients

Souhaitez-vous que nous vous envoyions un message lorsque des réductions seront disponibles?

Me rappeler plus tard

Merci ! Veuillez vérifier votre boîte de réception e-mail pour confirmer.

Oups ! Les notifications sont désactivées.