N,N-Dimethylformamide Dimethyl Acetal（DMF-DMA） - ≥98%, for esterfication , CAS No.4637-24-5

CAS: 4637-24-5 Cat. No.: D106289 Peso molecular: 119.16 Beilstein Registry Number: 506020 Número EC: 225-063-3

GRADE & PURITY ≥98%, for esterfication

Synonyms

dimetylformamide dimethyl acetal | DMF dimethylacetal | n,n-dimethylformamid-dimethylacetal | N,N-Dimethylformamidedimethylacetal | n,n-dimethylformamide-dimethylacetal | 1,1-Dimethoxy-N,N-dimethylmethylamine | 1,1-Dimethoxy-N,N-dimethyl-methylamine | dim

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

dimetylformamide dimethyl acetal | DMF dimethylacetal | n, n-dimethylformamid-dimethylacetal | N, N-Dimethylformamidedimethylacetal | n, n-dimethylformamide-dimethylacetal | 1, 1-Dimethoxy-N, N-dimethylmethylamine | 1, 1-Dimethoxy-N, N-dimethyl-methylamine | dim

Especificaciones y pureza

≥98%, for esterfication

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504755279
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755279
• Sonrisas canónicas: CN(C)C(OC)OC
• IUPAC Name: 1,1-dimethoxy-N,N-dimethylmethanamine
• InChIKey: ZSXGLVDWWRXATF-UHFFFAOYSA-N
• INCHI: 1S/C5H13NO2/c1-6(2)5(7-3)8-4/h5H,1-4H3
• Isómeros SMILES: CN(C)C(OC)OC
• WGK Alemania: 2
• Número ONU: 1993
• Peso molecular: 119.16
• Beilstein: 506020
• Reaxy-Rn: 506020
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506020&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Orthocarboxylic acid derivatives
      • Subclass Carboxylic acid amide acetals

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Orthocarboxylic acid derivatives
• Subclass: Carboxylic acid amide acetals
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid amide acetals
• Alternative Parents: Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Amide acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acid amide acetals. These are carboxylic acid derivatives two hydroxyl groups attached to a carbon atom, which in turn is linked to a nitrogen atom(substituted or not).
• External Descriptors: tertiary amino compound - acetal

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

Propiedades químicas y físicas

• Sensibilidad: Moisture Sensitive
• Índice de refracción: 1.3972
• Punto de inflamación (°F): 42.8 °F
• Punto de inflamación (°C): 7℃
• Punto de ebullición (°C): 104-108°C
• Punto de fusión (°C): -85°C
• Peso molecular: 119.160 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 119.095 Da
• Monoisotopic Mass: 119.095 Da
• Topological Polar Surface Area: 21.700 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 52.400
• 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

Referencias

1. Hailin Zhang, Tingting Zhou, Xiangyu Li, Wenbiao Xu, Junyou Shi.  (2025)  Efficient green Pre-Treatment of coniferous biomass using Alkali-Assisted deep eutectic solvents for tall oil production and lignin component separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.131474]

2. Pengtao Yuan, Xi Jiang, Xintong Ni, Xusheng Shao, Xuhong Qian, Qing Yang.  (2025)  Discovery of conformation constrained tetracyclic compounds as potent chitinase OfChi-h inhibitors with a novel binding mode.  JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY,      [PMID:40619956] [10.1080/14756366.2025.2528056]

3. Lingyu Chen, Yunhong Liu, Xinyan Peng, Yuelan Wei, Ke Shao.  (2025)  Simultaneous hypercrosslinking and functionalization of porous polystyrene adsorbent for protein-bound uraemic toxins removal.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2025.106265]