Dichloromethane Standard - 2000ug/ml in Purge and Trap Methanol , CAS No.75-09-2

CAS: 75-09-2 Cat. No.: D128117 Formule: CH2Cl2 Poids moléculaire: 84.93 Beilstein Registry Number: 1730800 Numéro CE: 200-838-9 PubChem CID: 6344
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ 2000ug/ml in Purge and Trap Methanol
Synonyms
Methyledichloride Methylene chloride
Storage
Room temperature,Argon charged
Shipped In
FedEx DG Service
★
Taille
Allemagne (EU)
USA*
Prix
Qté
1ml
D128117-1ml
—
3 En stock

163,05€

192,55€
Enregistrer 29,50 € (15.32%)
Enter a quantity for the sizes you want to add.
🧪
Pourquoi cette qualité

2000ug/ml in Purge and Trap Methanol pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

🌡

Stockage & expédition

Room temperature,Argon charged Expédition FedEx DG Service. 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 2378 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Volatile Organic Compounds (VOCs) Single Component Standards US EPA Methods:502.2,524.2,8021,8021A,8021B,624,8240B,8260B

Spécifications

Synonymes
Methyledichloride Methylene chloride
Spécifications et pureté
2000ug/ml in Purge and Trap Methanol
Conditions de stockage de stockage
Room temperature,Argon charged
Expédié en
FedEx DG Service
Noms et identifiants
Isomères SMILES
C(Cl)Cl
WGK Allemagne
1
RTECS
PA8050000
PubChem CID
6344
Numéro ONU
1593
Groupe d'emballage
III
Poids moléculaire
84.93
Beilstein
1730800

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.

3 results found

Lot NumberCertificate TypeDateArticle
I1906076I1906076Certificate of AnalysisSep 07, 2026 D128117
K2112642K2112642Certificate of AnalysisSep 09, 2022 D128117
D2230072D2230072Certificate of AnalysisMar 11, 2022 D128117
Propriétés chimiques et physiques
SensibilitéLight Sensitive
Indice de réfraction1.424
Point d'ébullition (°C)40°C
Point de fusion (°C)-95.1°C
FAQ et articles
A New Esterification Method — Rapid Esterification Mediated by the Coupling Reagent NDTP
Distillation Grade Reagents: Definition, Quality Control and Representative Aladdin Products
Minute-Scale Construction of Fluorinated Nitrogen-Bridged Bicycles: Pd(II)/Pd(IV) Cascade Chemistry and a Pd(IV) “Dyotropic (Paired-Migration)” Rearrangement Driving Strain-Release Ring Expansion
Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)
TEMPO-Catalyzed Oxidation Quick Reference (Alcohol Oxidation Focus): Three Regeneration Routes (NaOCl / Cu–O₂ / PIDA) + Selection & Troubleshooting
A Complete Guide to Choosing Resins for SPPS (Solid-Phase Peptide Synthesis): Fmoc/Boc Routes, C-Terminal Acid/Amide, and a Key-Parameter Navigator
Structural–Functional Analysis of the Methoxy Group (–OCH₃) in Approved Small-Molecule Drugs: Mechanisms, Evidence Chains, and Product-Selection Navigation (with Related Product Tables)
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
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
New Progress in the Solid-Phase Synthesis of Sterically Hindered Peptides: Background, Core Breakthroughs, and Implications for Automation Compatibility of the RMMR Strategy
The Core Value of the Trityl Family of Protecting Groups: Acid-Deprotection Hierarchies and Selective Route Design
Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids
The Methodological Value of HATU in Difficult Couplings: Reactivity Advantages, Stereochemical Retention, and Condition Management
Low Racemization in Peptide Synthesis Is Not Just About Reagent Choice: Stereochemical Risk During the Activation Stage and Practical Strategies for Experimental Control
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
The Methodological Value of TCFH: Advantages in Challenging Amidation and the Switching Logic of Carboxylic Acid Activation Pathways
Low-Racemization Control in Peptide Synthesis: An Inverse N→C Peptide Synthesis Strategy via Activated α-Aminoesters
Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression
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
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization
Experimental Judgment for Differential Deprotection of Double Boc and Related N-Boc Systems: Substrate Type, Site-Response Differences, and Initial Condition Selection
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
From Planar Patterns to Self-Supporting Structures: The 3D Printing Formation Logic of High-Content Graphene Composite Inks
How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions
Peptide Intermediates Difficult to Dissolve and Separate? Route Design and Workup Strategies for Tag-Assisted Liquid-Phase Peptide Synthesis (TAG-LPPS)
AITF-Mediated Carboxylic Acid Activation for the Synthesis of Amides, Peptides, and Esters: Activation Mechanism and Applicable Scenarios
Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples
In Vitro Exposure Simulation and Bioaccessibility Assessment of Particulate Chemicals from Consumer Products Using Simulated Lung Fluid
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
From Nitroarenes to Pharmaceutically Relevant Pyridines: A Photochemically Induced Aryl Nitrene-Mediated Skeletal Editing Strategy
Direct O-Alkylation of Bicyclo[1.1.1]pentan-1-ol: Avoiding Alkoxide-Mediated Skeletal Fragmentation through Electrophile Activation
How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example
1,8-Naphthyridine-Based Aldose Reductase Inhibitors: Scaffold Construction, In Vitro Inhibitory Activity, and Directions for Structural Optimization
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
Solid Supports in Packed Gas Chromatography Columns: Definition, Mechanisms of Action, Classification, and Selection
Selectivity Mechanism of the Triple Aryne–Tetrazine Cascade Reaction: Reaction-Pathway Switching and Intermediate Transformations
Reaction Mechanism of Pyrrole Skeletal Recasting: Reconstruction of Intraring Atomic Connectivity during Dearomatization—Skeletal Reorganization—Rearomatization
Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis
Tether Effects in Intramolecular [2+2] Photocycloadditions: Straight and Crossed Regioselectivity and Stepwise C–C Bond Formation
Regioselectivity of Pyridine-Diimine (PDI)–Cobalt-Catalyzed Simmons–Smith-Type Cyclopropanation: Alkene Substitution Patterns and the Methylene-Transfer Mechanism
ACT-1014-6470 Kilogram-Scale Synthesis: N7-Selective Reductive Amination of an Unprotected Pyrazole, Subsequent N2 Alkylation, and Intramolecular Urea Formation
How to Evaluate Reaction Generality through Substrate Scope: From the Number of Examples to Standardized Substrate Selection
Citations of This Product
Calculateurs de solution
Avis

Avis des clients

Foire aux questions

How should this product be stored?
Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.
How is this product shipped?
This product is classified as dangerous goods and ships via FedEx DG Service. Ground and other economy services are not available, and delivery to some destinations or address types may be restricted.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 75-09-2, the molecular formula is CH2Cl2, and the molecular weight is 84.93 g/mol.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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.