| Identification | More |  [Name]
  N,N-Dimethylformamide dimethyl acetal |  [CAS]
  4637-24-5 |  [Synonyms]
  1,1-DIMETHOXY-N,N-DIMETHYL METHANAMINE 1,1-DIMETHOXY-N,N-DIMETHYLMETHYLAMINE 1,1-DIMETHOXYTRIMETHYLAMINE AURORA KA-683 DIMETHYLFORMAMIDEDIMETHYLACETAL DMF-DIMETHYLACETAL DMF-DMA METHYL-8 METHYL-8 REAGENT METHYL-8(R) REAGENT N-DIMETHOXYMETHYL-N,N-DIMETHYLAMINE N,N-DIMETHYLDIMETHOXYMETHYLAMINE N,N-DIMETHYLFORMAMIDE DIMETHYL ACETAL 1,1-dimethoxy-n,n-dimethyl-methanamin Dimethoxy(dimethylamino)methane Dimethoxy-N,N-dimethylmethanamine N-(Dimethoxymethyl)dimethylamine N,N-Dimethylfirmanmidedimethylacetal Trimethylamine, 1,1-dimethoxy- DMFDMA (DMFA) |  [EINECS(EC#)]
  225-063-3 |  [Molecular Formula]
  C5H13NO2 |  [MDL Number]
  MFCD00008482 |  [Molecular Weight]
  119.16 |  [MOL File]
  4637-24-5.mol |  
 | Chemical Properties | Back Directory |  [Appearance]
  clear colourless liquid |  [Melting point ]
  -85°C |  [Boiling point ]
  102-103 °C/720 mmHg (lit.) |  [density ]
  0.897 g/mL at 25 °C(lit.) 
 |  [vapor pressure ]
  34.5hPa at 20℃ |  [refractive index ]
  n20/D 1.396(lit.) 
 |  [Fp ]
  45 °F 
 |  [storage temp. ]
  Flammables area |  [solubility ]
  Miscible with most organic solvents. |  [form ]
  Solid |  [pka]
  5.00±0.50(Predicted) |  [color ]
  White to off-white |  [PH]
  7 (H2O) |  [explosive limit]
  1.3-17.7%(V) |  [Water Solubility ]
  hydrolysis |  [Sensitive ]
  Moisture Sensitive |  [Detection Methods]
  GC,NMR |  [BRN ]
  506020 |  [Exposure limits]
  ACGIH: TWA 200 ppm; STEL 250 ppm (Skin) OSHA: TWA 200 ppm(260 mg/m3) NIOSH: IDLH 6000 ppm; TWA 200 ppm(260 mg/m3); STEL 250 ppm(325 mg/m3) |  [LogP]
  0.750 (est) |  [CAS DataBase Reference]
  4637-24-5(CAS DataBase Reference) |  [NIST Chemistry Reference]
  Methanamine, 1,1-dimethoxy-N,N-dimethyl-(4637-24-5) |  [Storage Precautions]
  Moisture sensitive |  [EPA Substance Registry System]
  4637-24-5(EPA Substance) |  
 | Safety Data | Back Directory |  [Hazard Codes ]
  F,Xn,Xi |  [Risk Statements ]
  R11:Highly Flammable. R22:Harmful if swallowed. R36/37/38:Irritating to eyes, respiratory system and skin . R36/38:Irritating to eyes and skin . R20:Harmful by inhalation. R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . R10:Flammable. |  [Safety Statements ]
  S16:Keep away from sources of ignition-No smoking . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37:Wear suitable protective clothing and gloves . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S33:Take precautionary measures against static discharges . S29:Do not empty into drains . S7/9:Keep container tightly closed and in a well-ventilated place . |  [RIDADR ]
  UN 3271 3/PG 2 
 |  [WGK Germany ]
  1 
 |  [F ]
  21 |  [Autoignition Temperature]
  155 °C |  [TSCA ]
  Yes |  [HazardClass ]
  3 |  [PackingGroup ]
  II |  [HS Code ]
  29225000 |  [Toxicity]
  LD50 orally in Rabbit: > 5000 mg/kg |  
 | Hazard Information | Back Directory |  [Chemical Properties]
  clear colourless liquid |  [Uses]
  1,1-Dimethoxy-N,N-dimethylmethanamine is used as a reagent in the formation of pyridine derivatives that exhibit inhibition against PI3 kinase p110α enzymes. |  [Definition]
  ChEBI: An acetal obtained by formal condensation of N,N-dimethylformamide with methanol. N,N-dimethylformamide dimethyl acetal is a derivatisation agent used in gas-chromatography applica
ions |  [General Description]
 
 Esterate M (N,N-Dimethylformamide dimethyl acetal, DMFDMA) is an methylating reagent. It has been used in methyl esterification of carboxylic acid and also in one-step derivatization of amino acids into N,N-Dimethylaminomethylene methyl esters.  |  [Flammability and Explosibility]
  Highlyflammable |  [reaction suitability]
  reagent type: derivatization reagent reaction type: Acylations reagent type: derivatization reagent reaction type: Esterifications |  [Synthesis]
 
 A method for synthesizing N,N-dimethylformamide dimethyl acetal, comprising the steps of (1) heating N,N-dimethylformamide to 70°C, mixing with dimethyl sulfate in a molar ratio of 1:1 and reacting for 4 hours after the end of dropwise addition to obtain the imine complex, and then cooling to room temperature; (2) adding solid sodium methanol to 200 solvent oil, dispersing it by ultrasonication, adjusting the temperature to 25 ℃ and maintained, dropwise addition of the imine complex, the reaction for 2 hours and then filtered, the filtrate often pressure fractionation, collection of 105-108 ℃ fraction, to obtain N,N-dimethylformamide dimethyl acetal, the yield was 75.3%, purity of 97%; wherein the molar ratio of sodium methanol to the imine complex is 1:1. The synthesis of the N,N-dimethylformamide dimethyl acetal of Example 6 is the same as that of Example 2, the The difference is that the organic solvent of this embodiment is a mixed solvent oil: D40 solvent oil, D60 solvent oil and 260 solvent oil, with a volume ratio of 2:1:1, to obtain N,N-dimethylformamide dimethyl acetal with a yield of 85.4% and a purity of 97%.  |  [References]
  [1] Patent: CN106083611,  2016,  A. Location in patent: Paragraph 0034-0037; 0048-0049 |  
  
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