N,N-Dimethylformamide (DMF) - UPSSS grade, Single metal impurity ≤ 0.01ppb , CAS No.68-12-2

CAS: 68-12-2 Cat. No.: D1523990 Formula: C3H7NO Peso molecolare: 73.09 Beilstein Registry Number: 605365 Numero EC: 200-679-5
Disponibile su ordine
QUALITÀ & PUREZZA UPSSS grade ? UPSSS grade — the highest ultra-pure semiconductor tier in this series. Use for the most contamination-sensitive leading-edge processes. Single metal impurity ≤ 0.01ppb
Storage
Room temperature,Argon charged
Shipped In
Normal
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Dimensione
Germania (EU)
USA*
Prezzo
Qtà
500ml
D1523990-500ml
Su ordinazione · 8–12 settimane
2.898,16€
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Perché questa qualità

UPSSS grade, Single metal impurity ≤ 0.01ppb Livello "Upsss" per flussi di lavoro cromatografici e analitici sensibili che richiedono un'interferenza minima della linea di base.

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Stoccaggio e spedizione

Room temperature,Argon charged Spedizione Normal. Consultare il COA specifico del lotto per le specifiche esatte.

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Documenti di qualità

SDS, COA, scheda tecnica e scheda delle specifiche disponibili per il download. COA specifico del lotto accessibile tramite ricerca per numero di lotto.

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Prova documentale

Citato in 9509 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Specifiche

Specifiche e purezza
UPSSS grade, Single metal impurity ≤ 0.01ppb
Condizioni di conservazione di stoccaggio
Room temperature,Argon charged
Spedito in
Normal
Grado
Livello "Upsss"
Nomi e identificatori
Sorrisi canonici
CN(C)C=O
IUPAC Name
N,N-dimethylformamide
InChIKey
ZMXDDKWLCZADIW-UHFFFAOYSA-N
INCHI
1S/C3H7NO/c1-4(2)3-5/h3H,1-2H3
Isomeri SMILES
CN(C)C=O
WGK Germania
1
RTECS
LQ2100000
Numero UN
2265
Gruppo di imballaggio
III
Peso molecolare
73.09
Beilstein
605365
Reaxy-Rn
605365
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605365&ln=

Documentazione

📋 Scheda di dati di sicurezza (SDS)

Documento completo su pericoli, manipolazione, stoccaggio e conformità normativa.

<<<<<<< HEAD Scarica SDS → ======= Scarica SDS → >>>>>>> release248-p3

✅ Certificato di analisi (COA)

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📊 Scheda tecnica

Riepilogo di riferimento rapido delle specifiche e applicazioni del prodotto.

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🔬 Scheda delle specifiche

Attributi di qualità completi e criteri di accettazione per questa qualità.

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Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid amides
Direct ParentTertiary carboxylic acid amides
Alternative Parents Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Tertiary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as tertiary carboxylic acid amides. These are compounds containing an amide derivative of carboxylic acid, with the general structure RN(R1)C(R2)=O (R1-R2 any atom but H).
External Descriptors a small molecule
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
SensibilitàMoisture sensitive.
Indice di rifrazione1.4269
Punto di infiammabilità (°F)136.4 °F
Punto di infiammabilità (°C)58℃
Punto di ebollizione (°C)152.8°C
Punto di fusione (°C)-61°C
Peso molecolare73.090 g/mol
XLogP3-1.000
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass73.0528 Da
Monoisotopic Mass73.0528 Da
Topological Polar Surface Area20.300 Ų
Heavy Atom Count5
Formal Charge0
Complexity33.900
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
Domande frequenti e articoli
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
Sulfonyl Hydrazide-Mediated Introduction of Small C(sp³) Fragments: Nickel-Catalyzed Cross-Coupling, Medicinal Chemistry Applications, and Reagent Selection
From Nucleophilic to Electrophilic BCB Synthetic Equivalents: Hypervalent-Iodine-Mediated Umpolung Design
From Functional-Group Transformation to Intramolecular Cyclization: Reaction-Pathway Analysis of TMSCl/DMF-Promoted Annulation and CuCN-Mediated Cascade Cyclization
Medicinal Chemistry Design of the Indazole Scaffold: Tautomerism, Molecular Recognition, Substitution-Site Design, and Synthetic Strategies
Discovery and Structural Optimization of the Noncovalent 3CL Protease Inhibitor S-217622
How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example
How to Bypass α-Fluoride Elimination: Bromine-Transfer Capture and Oxidative Coupling of α,α-Difluorobenzylic Anions
Reactions and Applications of 3,3-Difluoroallyl Sulfonium Salts (DFASs): Small-Molecule gem-Difluoroallylation, Selective Peptide Modification, and Subsequent Functionalization
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
Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies
Copper Tripeptide GHK-Cu and Skin Repair: From Copper Coordination Chemistry to Extracellular Matrix Remodeling
Direct Construction of Methylsulfonyl-Containing Heterocycles: Synthesis and Applications of Prefunctionalized Three-Carbon Vinamidinium Salts
Tether Effects in Intramolecular [2+2] Photocycloadditions: Straight and Crossed Regioselectivity and Stepwise C–C Bond Formation
Screening and Replacement of Green Solvents in Metallaphotoredox Catalysis: Reaction Compatibility and Process Feasibility
ACT-1014-6470 Kilogram-Scale Synthesis: N7-Selective Reductive Amination of an Unprotected Pyrazole, Subsequent N2 Alkylation, and Intramolecular Urea Formation
Bond-Formation Sequence and Process Improvement for 3-Bromo-6-alkyl-1,6-naphthyridin-5(6H)-ones: From Late-Stage N-Alkylation to Enamine Cyclization with Primary Amines
Citations of This Product
Calcolatori di soluzioni
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