Cas no 851377-62-3 (1-sec-Butylhydrazine Hydrochloride)

1-sec-Butylhydrazine Hydrochloride structure
851377-62-3 structure
Product Name:1-sec-Butylhydrazine Hydrochloride
CAS No:851377-62-3
MF:C4H13ClN2
MW:124.612419843674
CID:1838907
PubChem ID:43819151
Update Time:2025-11-01

1-sec-Butylhydrazine Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • sec-Butylhydrazine hydrochloride (1:1)
    • BS-22325
    • CS-0210628
    • Hydrazine, (1-methylpropyl)-, monohydrochloride
    • sec-Butylhydrazine hydrochloride(1:x)
    • AB8698
    • AKOS026676559
    • sec-butylhydrazine hydrochloride
    • sec-Butylhydrazinehydrochloride(1:x)
    • SEC-BUTYLHYDRAZINE HCL
    • 851377-62-3
    • EN300-175545
    • Butan-2-ylhydrazine hydrochloride
    • 1672653-21-2
    • DB-191346
    • butan-2-ylhydrazine;hydrochloride
    • AB92365
    • (butan-2-yl)hydrazine hydrochloride
    • F8880-3601
    • SCHEMBL2075807
    • Butan-2-ylhydrazine HCl
    • 1-Sec-butylhydrazine hydrochloride
    • 1-sec-Butylhydrazine Hydrochloride
    • MDL: MFCD13806973
    • Inchi: 1S/C4H12N2.ClH/c1-3-4(2)6-5;/h4,6H,3,5H2,1-2H3;1H
    • InChI Key: MAOHZRUELSGCPI-UHFFFAOYSA-N
    • SMILES: Cl.N(C(C)CC)N

Computed Properties

  • Exact Mass: 124.077
  • Monoisotopic Mass: 124.077
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 2
  • Complexity: 28.7
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 38A^2

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1-sec-Butylhydrazine Hydrochloride Related Literature

Additional information on 1-sec-Butylhydrazine Hydrochloride

Comprehensive Overview of 1-sec-Butylhydrazine Hydrochloride (CAS No. 851377-62-3): Properties, Applications, and Industry Insights

1-sec-Butylhydrazine Hydrochloride (CAS No. 851377-62-3) is a specialized organic compound widely recognized for its unique chemical properties and versatile applications in pharmaceutical and agrochemical research. This compound, characterized by its hydrazine derivative structure, has garnered significant attention due to its role as a key intermediate in synthetic chemistry. With the growing demand for high-purity chemical intermediates, researchers and manufacturers are increasingly focusing on optimizing its synthesis and applications.

The molecular formula of 1-sec-Butylhydrazine Hydrochloride reflects its secondary butyl group, which contributes to its stability and reactivity in various chemical reactions. Its CAS No. 851377-62-3 serves as a critical identifier in global chemical databases, ensuring accurate classification and regulatory compliance. Recent trends in green chemistry and sustainable synthesis have spurred innovations in the production of such intermediates, aligning with the industry's shift toward environmentally friendly practices.

In pharmaceutical applications, 1-sec-Butylhydrazine Hydrochloride is often utilized as a building block for active pharmaceutical ingredients (APIs). Its ability to form stable bonds with other functional groups makes it invaluable in designing novel drug candidates. For instance, it has been explored in the development of central nervous system (CNS) therapeutics, a rapidly growing sector driven by increasing neurological disorder cases worldwide. Researchers are also investigating its potential in cancer research, particularly in the synthesis of targeted therapies.

The agrochemical industry leverages 1-sec-Butylhydrazine Hydrochloride for formulating crop protection agents. Its structural features enable the creation of compounds with enhanced efficacy against pests while minimizing environmental impact. As the demand for sustainable agriculture solutions rises, this compound's role in developing biodegradable pesticides has become a focal point. Regulatory agencies emphasize the need for safer alternatives, further driving research into derivatives of hydrazine-based compounds.

From a technical perspective, the synthesis of 1-sec-Butylhydrazine Hydrochloride involves precise control of reaction conditions to ensure high yield and purity. Advanced techniques such as flow chemistry and catalytic hydrogenation are being adopted to improve efficiency. Analytical methods like HPLC and NMR spectroscopy are critical for quality assurance, addressing the stringent standards required in industrial and academic settings.

Market dynamics for 1-sec-Butylhydrazine Hydrochloride reflect broader trends in the fine chemicals sector. With Asia-Pacific emerging as a hub for chemical manufacturing, supply chain resilience and cost-effective production are key considerations. Companies are investing in process optimization and scale-up technologies to meet global demand while adhering to REACH and other regulatory frameworks.

Safety and handling protocols for 1-sec-Butylhydrazine Hydrochloride emphasize proper storage and handling to maintain stability. While not classified as hazardous under standard conditions, best practices include using personal protective equipment (PPE) and ensuring adequate ventilation in laboratory environments. These precautions align with industry-wide efforts to enhance workplace safety in chemical research and production.

Future prospects for 1-sec-Butylhydrazine Hydrochloride are closely tied to advancements in precision medicine and smart farming. As interdisciplinary research expands, its applications in material science and nanotechnology are also being explored. Collaborative efforts between academia and industry will likely unlock new functionalities, reinforcing its importance in modern chemistry.

In summary, 1-sec-Butylhydrazine Hydrochloride (CAS No. 851377-62-3) represents a critical component in the toolkit of synthetic chemists. Its multifaceted applications, coupled with ongoing innovations in production and utilization, position it as a compound of enduring relevance. As industries evolve toward sustainability and efficiency, this hydrazine derivative will continue to play a pivotal role in shaping the future of chemical research and development.

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