Cas no 6006-65-1 (N,N-Dimethylformamide dipropyl acetal)

N,N-Dimethylformamide dipropyl acetal (CAS: 118440-14-1) is a versatile reagent commonly employed in organic synthesis as a protecting group for aldehydes and ketones. Its key advantages include high reactivity under mild conditions, enabling selective protection without affecting other functional groups. The compound is particularly useful in multistep syntheses due to its stability and ease of deprotection under acidic conditions. Additionally, it serves as a precursor in the preparation of formamidines and other nitrogen-containing intermediates. Its dipropyl acetal structure enhances solubility in nonpolar solvents, facilitating reactions in diverse media. This reagent is valued for its reliability in complex transformations, making it a practical choice for synthetic chemists.
N,N-Dimethylformamide dipropyl acetal structure
6006-65-1 structure
Product Name:N,N-Dimethylformamide dipropyl acetal
CAS No:6006-65-1
MF:C9H21NO2
MW:175.26854300499
MDL:MFCD00009374
CID:46326
PubChem ID:24850754
Update Time:2025-11-02

N,N-Dimethylformamide dipropyl acetal Chemical and Physical Properties

Names and Identifiers

    • N,N-Dimethylformamide dipropyl acetal
    • 1,1-Dipropoxytrimethylamine
    • N,N-Dimethylformamide di-n-propyl acetal
    • N,N-Dimethylforamide di-n-propyl acetal (for esterification)
    • N,N-Dimethylformamide Dipropyl Acetal [for Esterification]
    • N,N-dimethyl-1,1-dipropoxymethanamine
    • 1,1-Dipropoxy-N,N-dimethylmethylamine
    • N,N-DIMETHYLFORMAMIDEDIPROPYLACETAL
    • AKOS024348828
    • NS00047032
    • CS-0099674
    • D1301
    • (dipropoxymethyl)dimethylamine
    • dimethylformamide dipropyl acetal
    • N,N-Dimethylformamide dipropyl acetal, for GC derivatization
    • Methanamine, N,N-dimethyl-1,1-dipropoxy-
    • FT-0629540
    • n,n-dimethylformamide dipropylacetal
    • MFCD00009374
    • N,N-Dimethylformamide dipropyl acetal, 97%
    • SCHEMBL132624
    • EINECS 227-855-4
    • InChI=1/C9H21NO2/c1-5-7-11-9(10(3)4)12-8-6-2/h9H,5-8H2,1-4H3
    • DTXSID60208787
    • N,N-Dimethyl(dipropoxy)methanamine #
    • N,N-Dimethylformamide dipropyl acetal for gc derivatization
    • 6006-65-1
    • W-105281
    • NSLGQFIDCADTAS-UHFFFAOYSA-
    • N,N -Dimethylformamide Dipropyl Acetal [for Esterification]
    • DB-053523
    • G69986
    • MDL: MFCD00009374
    • Inchi: 1S/C9H21NO2/c1-5-7-11-9(10(3)4)12-8-6-2/h9H,5-8H2,1-4H3
    • InChI Key: NSLGQFIDCADTAS-UHFFFAOYSA-N
    • SMILES: O(CCC)C(N(C)C)OCCC
    • BRN: 1098524

Computed Properties

  • Exact Mass: 175.15700
  • Monoisotopic Mass: 175.157
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 7
  • Complexity: 88.5
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2
  • Topological Polar Surface Area: 21.7A^2

Experimental Properties

  • Color/Form: Not determined
  • Density: 0.854?g/mL?at 25?°C(lit.)
  • Boiling Point: 67-68?°C/14?mmHg(lit.)
  • Flash Point: Fahrenheit: 114.8 ° f
    Celsius: 46 ° c
  • Refractive Index: n20/D 1.409(lit.)
  • Water Partition Coefficient: It hydrolyzes with water.
  • PSA: 21.70000
  • LogP: 1.68480
  • Solubility: Not determined
  • Sensitiveness: Moisture Sensitive
  • Vapor Pressure: 1.1±0.3 mmHg at 25°C

N,N-Dimethylformamide dipropyl acetal Security Information

  • Symbol: GHS02 GHS07
  • Prompt:warning
  • Signal Word:Warning
  • Hazard Statement: H226-H315-H319-H335
  • Warning Statement: P261-P305+P351+P338
  • Hazardous Material transportation number:UN 1993 3/PG 3
  • WGK Germany:3
  • Hazard Category Code: 36/37/38
  • Safety Instruction: S26-S36
  • Hazardous Material Identification: Xi
  • Packing Group:III
  • Hazard Level:3
  • Safety Term:3
  • Packing Group:III
  • Risk Phrases:R36/37/38
  • HazardClass:3
  • PackingGroup:III
  • Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)

N,N-Dimethylformamide dipropyl acetal Customs Data

  • HS CODE:29225000
  • Customs Data:

    China Customs Code:

    2922199090

    Overview:

    2922199090. Other amino alcohols and their ethers,Esters and their salts(Except those containing more than one oxygen-containing group). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Summary:

    2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

N,N-Dimethylformamide dipropyl acetal Pricemore >>

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N,N-Dimethylformamide dipropyl acetal Related Literature

Additional information on N,N-Dimethylformamide dipropyl acetal

N,N-Dimethylformamide Dipropyl Acetal (CAS 6006-65-1): A Versatile Chemical Reagent for Modern Applications

N,N-Dimethylformamide dipropyl acetal (CAS 6006-65-1), often abbreviated as DMF dipropyl acetal, is a specialized organic compound that has garnered significant attention in synthetic chemistry and industrial applications. This chemical reagent belongs to the class of acetals, which are widely used as protecting groups for carbonyl compounds and as intermediates in organic synthesis. With the increasing demand for efficient and selective chemical transformations, N,N-dimethylformamide dipropyl acetal has emerged as a valuable tool for researchers and manufacturers alike.

The molecular structure of N,N-dimethylformamide dipropyl acetal features a dimethylformamide moiety coupled with a dipropyl acetal group, making it a unique reagent for various chemical reactions. Its CAS number 6006-65-1 serves as a unique identifier in chemical databases, ensuring accurate referencing in scientific literature and regulatory documents. The compound's stability under mild conditions and its ability to participate in diverse reactions have made it a subject of interest in both academic and industrial settings.

One of the most prominent applications of DMF dipropyl acetal is its use as a protecting group in organic synthesis. Protecting groups are essential for temporarily masking reactive functional groups during multi-step syntheses, and N,N-dimethylformamide dipropyl acetal offers distinct advantages in this regard. Its compatibility with a wide range of reaction conditions and its ease of removal under specific circumstances make it a preferred choice for synthetic chemists working on complex molecular architectures.

In recent years, the growing interest in green chemistry and sustainable synthetic methods has led researchers to explore the potential of N,N-dimethylformamide dipropyl acetal in environmentally friendly processes. The compound's ability to facilitate reactions under mild conditions often reduces energy consumption and minimizes waste generation, aligning with the principles of green synthesis. This aspect has become particularly relevant as industries worldwide strive to meet increasingly stringent environmental regulations and consumer demands for sustainable products.

The pharmaceutical industry has shown considerable interest in CAS 6006-65-1 due to its utility in drug discovery and development. DMF dipropyl acetal serves as a valuable building block in the synthesis of various drug candidates, particularly those containing sensitive functional groups that require protection during synthetic sequences. Its application in the preparation of active pharmaceutical ingredients (APIs) has been documented in several patent applications, highlighting its importance in modern medicinal chemistry.

Material science represents another field where N,N-dimethylformamide dipropyl acetal finds significant application. The compound's unique properties make it suitable for modifying polymer structures and creating specialized materials with tailored characteristics. Researchers have utilized DMF dipropyl acetal in the development of advanced materials for electronics, coatings, and specialty adhesives, where precise control over molecular architecture is crucial for achieving desired performance properties.

From a commercial perspective, the market for N,N-dimethylformamide dipropyl acetal has shown steady growth, driven by increasing demand from research institutions and chemical manufacturers. Suppliers of CAS 6006-65-1 typically offer the compound in various purity grades to meet different application requirements, from laboratory-scale research to industrial production. The global supply chain for this specialty chemical remains robust, with manufacturers implementing strict quality control measures to ensure consistency and reliability.

Handling and storage of DMF dipropyl acetal require standard laboratory precautions. While not classified as hazardous under normal conditions, proper storage in sealed containers away from moisture and strong oxidizing agents is recommended to maintain its stability and shelf life. These handling considerations make N,N-dimethylformamide dipropyl acetal a practical choice for various laboratory and industrial settings where safety and ease of use are important factors.

The analytical characterization of CAS 6006-65-1 typically involves standard techniques such as nuclear magnetic resonance (NMR) spectroscopy, infrared spectroscopy, and mass spectrometry. These methods allow for precise identification and purity assessment of N,N-dimethylformamide dipropyl acetal, ensuring its suitability for sensitive applications. Quality control protocols often include these analytical techniques to guarantee batch-to-batch consistency in commercial products.

Recent advancements in synthetic methodology have expanded the potential applications of DMF dipropyl acetal. Novel catalytic systems and reaction conditions continue to be developed that leverage the unique properties of this compound, opening new possibilities in organic synthesis. These developments align with current trends in chemical research that emphasize atom economy, selectivity, and process efficiency – all areas where N,N-dimethylformamide dipropyl acetal can contribute significantly.

Looking to the future, research on CAS 6006-65-1 is expected to focus on expanding its synthetic utility and exploring new applications in emerging technologies. Areas such as renewable energy materials, nanotechnology, and biomedical engineering may benefit from the unique properties of N,N-dimethylformamide dipropyl acetal. As chemical science continues to evolve, this versatile reagent is likely to maintain its importance in both fundamental research and industrial applications.

For researchers and professionals seeking information about DMF dipropyl acetal, reliable sources include peer-reviewed journals, chemical databases, and reputable suppliers' technical documentation. The compound's CAS number 6006-65-1 serves as a key identifier when searching for specific information, ensuring accurate retrieval of relevant data from scientific literature and material safety resources.

In conclusion, N,N-dimethylformamide dipropyl acetal (CAS 6006-65-1) represents a valuable chemical reagent with diverse applications across multiple scientific and industrial domains. Its unique properties as a protecting group and synthetic intermediate, combined with its compatibility with modern green chemistry principles, ensure its continued relevance in contemporary chemical research and production. As new applications emerge and synthetic methodologies advance, DMF dipropyl acetal is poised to remain an important tool in the chemist's repertoire.

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