Cas no 16883-45-7 (Tetramethylammonium borohydride)

Tetramethylammonium borohydride (TMABH) is a quaternary ammonium borohydride compound with the formula (CH?)?N[BH?]. It serves as a stable, soluble reducing agent, particularly useful in organic and inorganic synthesis. TMABH offers advantages such as high reactivity under mild conditions, selectivity in reducing carbonyl compounds, and compatibility with polar solvents like water and alcohols. Its ionic nature enhances solubility in various reaction media, facilitating homogeneous reactions. Additionally, TMABH is less hygroscopic compared to alkali metal borohydrides, improving handling and storage stability. These properties make it a valuable reagent for controlled reductions in pharmaceutical, materials, and fine chemical applications.
Tetramethylammonium borohydride structure
16883-45-7 structure
Product Name:Tetramethylammonium borohydride
CAS No:16883-45-7
MF:C4H12BN
MW:84.9557809829712
MDL:MFCD00011778
CID:50574
PubChem ID:87576685
Update Time:2025-06-08

Tetramethylammonium borohydride Chemical and Physical Properties

Names and Identifiers

    • Tetramethylammonium borohydride
    • Tetramethylammonium Borohydride [Reducing Reagent]
    • BISMUTH(III) SUBNITRATE
    • Tetra-methyl ammonium boron hydride
    • tetramethylammonium tetrahydroborate
    • tetramethyl-ammonium,tetrahydrido borate
    • Tetramethyl-ammonium,Tetrahydridoborat
    • tetramethylammoniumborohydrate
    • TMAB
    • NSC 164901
    • Tetramethylammonium Borohydride Tetramethylammonium borohydride,TMAB
    • Nsc164901
    • BISMUTH(III) SUBNITRATE 98%
    • Tetramethylammoniumborohydride,95%
    • TetraMethylaMMoniuM borohydride 95%
    • Tetramethylammonium borohydrate
    • Borohydride, polymer-supported
    • Tetramethylammonium tetrahydroborate(1-)
    • N,N,N-Trimethylmethanaminium tetrahydroborate(1-)
    • Tetramethylammonium tetrahydridoborate
    • AMMONIUM, TETRAMETHYL-, TETRAHYDROBORATE(1-)
    • Methanaminium, N,N,N-trimethyl-, tetrahydroborate(1-)
    • (Polystyrylmethyl)trimethylammonium borohydride
    • Met
    • DTXSID70937556
    • tetramethylazanium boranuide
    • Tetramethylammonium borohydride, 95%
    • TVQBZLPZXCVNEO-UHFFFAOYSA-N
    • EINECS 240-917-5
    • FT-0746664
    • N,N,N-Trimethylmethanaminium tetrahydroborate
    • AKOS025294695
    • J-010484
    • GS-5752
    • 16883-45-7
    • T0852
    • MDL: MFCD00011778
    • Inchi: 1S/C4H12N.B/c1-5(2,3)4;/h1-4H3;/q+1;-1
    • InChI Key: TVQBZLPZXCVNEO-UHFFFAOYSA-N
    • SMILES: [N+](C)(C)(C)C.[B-]

Computed Properties

  • Exact Mass: 88.12980
  • Monoisotopic Mass: 85.10628
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 6
  • Rotatable Bond Count: 0
  • Complexity: 19.1
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Topological Polar Surface Area: 0

Experimental Properties

  • Color/Form: Not determined
  • Density: 0.813(lit.)
  • Melting Point: 150°C (dec.)
  • Boiling Point: No data available
  • Flash Point: No data available
  • PSA: 0.00000
  • LogP: -0.86150
  • Sensitiveness: Moisture Sensitive
  • Solubility: Not determined
  • Vapor Pressure: No data available

Tetramethylammonium borohydride Security Information

Tetramethylammonium borohydride Pricemore >>

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Additional information on Tetramethylammonium borohydride

Comprehensive Guide to Tetramethylammonium Borohydride (CAS No. 16883-45-7): Properties, Applications, and Innovations

Tetramethylammonium borohydride (CAS No. 16883-45-7) is a versatile quaternary ammonium borohydride compound widely recognized for its role as a mild and selective reducing agent in organic synthesis. With the molecular formula (CH3)4N[BH4], this white crystalline solid exhibits unique solubility in polar solvents like water and methanol, making it indispensable in laboratories and industrial processes. Its low toxicity and high stability under controlled conditions have fueled its adoption in pharmaceuticals, materials science, and green chemistry initiatives.

Recent advancements in sustainable chemistry have spotlighted Tetramethylammonium borohydride as a eco-friendly alternative to traditional reductants like sodium borohydride. Researchers highlight its efficiency in asymmetric hydrogenation and catalytic transformations, addressing growing demand for precision synthesis in drug development. A 2023 study published in ACS Sustainable Chemistry & Engineering emphasized its potential to reduce waste in API (Active Pharmaceutical Ingredient) manufacturing, aligning with circular economy principles.

The compound’s thermal decomposition behavior and hydrogen storage capabilities have also garnered attention in energy research. Unlike volatile hydrides, 16883-45-7 releases hydrogen gas at moderate temperatures, prompting investigations into its use for fuel cell applications. Industry forums frequently discuss its integration with nanocatalysts to enhance reaction kinetics—a topic trending in AI-driven materials discovery platforms like MIT’s NanoHub.

From a commercial perspective, Tetramethylammonium borohydride suppliers emphasize batch consistency and GMP compliance to meet pharmaceutical standards. Analytical techniques such as FT-IR spectroscopy and X-ray diffraction are critical for verifying purity, as impurities can impact reaction yields in sensitive processes like peptide coupling. Regulatory databases like REACH and PubChem provide updated safety profiles, reinforcing its classification as a non-hazardous reagent when handled properly.

Emerging applications include its use in electronic materials deposition, where it serves as a reducing agent for copper interconnects in semiconductor fabrication. This aligns with the Internet of Things (IoT) sector’s demand for miniaturized components. Additionally, its role in synthesizing boron-doped graphene—a material explored for supercapacitors—has been cited in patents from IBM and Samsung.

For researchers optimizing cost-effective synthesis, Tetramethylammonium borohydride offers advantages over metal hydrides due to its lower corrosivity and easier byproduct management. Educational platforms like ScienceDirect feature protocols for its use in undergraduate chemistry labs, underscoring its pedagogical value. Meanwhile, patent analytics tools reveal a 40% increase in filings related to its derivatives since 2020, signaling robust R&D interest.

In summary, Tetramethylammonium borohydride (CAS No. 16883-45-7) bridges academic inquiry and industrial innovation. Its adaptability across green chemistry, energy storage, and advanced materials positions it as a future-forward chemical, while ongoing studies explore novel derivatives for biomedical imaging and carbon capture technologies.

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