N-N-Dimethylacetamide (DMAC) - electronic grade, UP grade, ≥99.8%(GC), used for N,N-Dimethylacetamide may be used as a solvent in the following processes: · Palladium (II) acetate-butyldi-1-adamantylphosphine catalyzed arylation of 2-isobutylthiazole with

CAS: 127-19-5 Cat. No.: D1523612 Fórmula: C₄H₉NO Peso molecular: 87.12 Beilstein Registry Number: 1737614 Número CE: 204-826-4

GRADE & PURITY Electronic grade, UP grade, ≥99.8%(GC)

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Visão geral

N,N-Dimethylacetamide, also known as acetyldimethylamine, abbreviated as DMAC, is an aprotic highly polar solvent with a slight ammonia odor. It has strong solvency and a wide range of soluble substances. It can be miscible with water, aromatic compounds, esters, ketones, alcohols, ethers, benzene, trichloromethane and other substances in any proportion, and can activate compound molecules. Therefore, it is widely used as a solvent and catalyst. 

As a solvent with high boiling point, high flash point, high thermal stability and chemical stability, it can be used as spinning solvent for polyacrylonitrile, and solvent for synthetic resins, natural resins, copolymers such as vinyl formate and vinyl pyridine, and aromatic carboxylic acids. As a catalyst, it can be used in processes such as heating urea to produce cyanuric acid, reacting alkyl halides with metal cyanides to produce nitriles, reacting sodium acetylide with alkyl halides to produce alkyl alkynes, and reacting organic halides with cyanates to produce isocyanates. N,N-dimethylacetamide can also be used as electrolytic solvent, solvent for photographic couplers, paint remover, raw material for organic synthesis, pesticide and pharmaceutical raw material, extractive distillation solvent for separating styrene from C8 distillate, etc.

Specifications

Especificações e pureza

electronic grade, UP grade, ≥99.8%(GC)

Aplicação

N,N-Dimethylacetamide may be used as a solvent in the following processes: · Palladium (II) acetate-butyldi-1-adamantylphosphine catalyzed arylation of 2-isobutylthiazole with chlorobenzene to form 5-phenyl-2-isobutylthiazole. · Synthesis of β-, γ-, and δ

Condições de armazenamento de armazenamento

Room temperature,Argon charged,Desiccated

Enviado em

Normal

Grau

Nível UP, Qualidade eletrónica

Pureza

≥99.8%(GC)

Nomes e identificadores

Sorrisos canónicos

CC(=O)N(C)C

IUPAC Name

N,N-dimethylacetamide

InChIKey

FXHOOIRPVKKKFG-UHFFFAOYSA-N

INCHI

1S/C4H9NO/c1-4(6)5(2)3/h1-3H3

SMILES isoméricas

CC(=O)N(C)C

WGK Alemanha

1

RTECS

AB7700000

Número UN

2810

Grupo de embalagem

I

Peso molecular

87.12

Beilstein

1737614

Reaxy-Rn

1737614

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1737614&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid amides
          • Level6 Tertiary carboxylic acid amides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid amides
• Direct Parent: Tertiary carboxylic acid amides
• Alternative Parents: Acetamides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acetamide - 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
• Descrição: This 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriedades químicas e físicas

• Solubilidade: Miscible with water, benzene, alcohol, acetone, ether, esters and ketones.
• Sensibilidade: Hygroscopic；Air sensitive
• Índice de refração: 1.4373
• Ponto de inflamação (°F): 147.2 °F
• Ponto de inflamação (°C): 70℃
• Ponto de ebulição (°C): 163-165°C
• Ponto de fusão (°C): -20°C
• Peso molecular: 87.120 g/mol
• XLogP3: -0.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 87.0684 Da
• Monoisotopic Mass: 87.0684 Da
• Topological Polar Surface Area: 20.300 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 58.600
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1