Cas no 3424-21-3 (Tris(isopropylamine))

Tris(isopropylamine) structure
Tris(isopropylamine) structure
Product Name:Tris(isopropylamine)
CAS No:3424-21-3
MF:C9H21N
MW:143.26974272728
CID:307538
PubChem ID:61924
Update Time:2025-04-23

Tris(isopropylamine) Chemical and Physical Properties

Names and Identifiers

    • 2-Propanamine,N,N-bis(1-methylethyl)-
    • N,N-di(propan-2-yl)propan-2-amine
    • Tri Isopropyl Amine
    • Triisopropyl-amine
    • Caswell No. 892
    • EINECS 222-317-5
    • N,N,N-triisopropylamine
    • Triisopropylamine
    • EPA Pesticide Chemical Code 004210
    • 2-Propanamine, N,N-bis(1-methylethyl)-
    • N,N-diisopropylpropane-2-amine
    • Q8214065
    • J-019518
    • AKOS006275559
    • thisopropylamine
    • tri-iso-propylamine
    • Tris(isopropylamine)
    • NS00029628
    • RKBCYCFRFCNLTO-UHFFFAOYSA-N
    • N,N-Bis(1-methylethyl)-2-propanamine
    • 3424-21-3
    • Y67CF9Z56L
    • tri-isopropylamin
    • UNII-Y67CF9Z56L
    • SCHEMBL22407
    • DTXSID1042493
    • N,N-diisopropylpropan-2-amine
    • DTXCID9022493
    • DB-210677
    • MDL: MFCD00674009
    • Inchi: 1S/C9H21N/c1-7(2)10(8(3)4)9(5)6/h7-9H,1-6H3
    • InChI Key: RKBCYCFRFCNLTO-UHFFFAOYSA-N
    • SMILES: N(C(C)C)(C(C)C)C(C)C

Computed Properties

  • Exact Mass: 143.16700
  • Monoisotopic Mass: 143.167
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 65.7
  • 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
  • Topological Polar Surface Area: 3.2A^2
  • XLogP3: 2.7

Experimental Properties

  • Density: 0.772
  • Boiling Point: 131.8°C at 760 mmHg
  • Flash Point: 21.9°C
  • Refractive Index: 1.424
  • PSA: 3.24000
  • LogP: 2.51360
  • Vapor Pressure: 9.1±0.2 mmHg at 25°C

Tris(isopropylamine) Security Information

Tris(isopropylamine) Customs Data

  • HS CODE:2921199090
  • Customs Data:

    China Customs Code:

    2921199090

    Overview:

    2921199090 Other acyclic monoamines and their derivatives and salts.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

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Additional information on Tris(isopropylamine)

Introduction to 2-Propanamine,N,N-bis(1-methylethyl)- (CAS No. 3424-21-3)

2-Propanamine,N,N-bis(1-methylethyl)-, identified by its Chemical Abstracts Service (CAS) number 3424-21-3, is a significant compound in the realm of organic chemistry and pharmaceutical research. This tertiary amine, characterized by its bulky isopropyl groups, exhibits unique structural and functional properties that make it a valuable intermediate in synthetic chemistry and drug development.

The molecular structure of 2-Propanamine,N,N-bis(1-methylethyl)- consists of a central nitrogen atom coordinated to two isopropyl groups, each derived from isobutane. This arrangement imparts steric hindrance, which influences its reactivity and solubility characteristics. The compound’s high boiling point and moderate solubility in organic solvents further enhance its utility in industrial and laboratory applications.

In recent years, 2-Propanamine,N,N-bis(1-methylethyl)- has garnered attention in the pharmaceutical industry due to its role as a building block for more complex molecules. Its tertiary amine functionality allows for facile participation in nucleophilic substitution reactions, making it a versatile precursor for synthesizing various pharmacologically active agents. For instance, researchers have explored its use in the preparation of novel antiviral and anti-inflammatory compounds, leveraging its ability to form stable complexes with biological targets.

One of the most compelling aspects of 2-Propanamine,N,N-bis(1-methylethyl)- is its stability under a range of chemical conditions. This stability is particularly advantageous in multi-step synthesis protocols where harsh reagents or elevated temperatures are employed. Additionally, the compound’s resistance to hydrolysis makes it suitable for long-term storage and transport, reducing the likelihood of degradation during handling.

The synthesis of 2-Propanamine,N,N-bis(1-methylethyl)- typically involves the reaction of isobutylene with ammonia in the presence of a suitable catalyst. This process, often conducted under controlled conditions to maximize yield and purity, highlights the compound’s industrial relevance. Recent advancements in catalytic systems have improved the efficiency of this synthesis, making it more cost-effective and environmentally friendly.

From an applications perspective, 2-Propanamine,N,N-bis(1-methylethyl)- finds use not only in pharmaceuticals but also in agrochemicals and specialty chemicals. Its ability to act as a chiral auxiliary in asymmetric synthesis has been explored for producing enantiomerically pure compounds, which are crucial in many drug formulations. Furthermore, its role as a surfactant and stabilizer in polymer formulations underscores its versatility across different chemical domains.

The safety profile of 2-Propanamine,N,N-bis(1-methylethyl)- is another critical consideration. While it does not exhibit acute toxicity at typical exposure levels, proper handling procedures must be followed to prevent skin and eye irritation. Personal protective equipment (PPE), such as gloves and safety goggles, is recommended when working with this compound. As with any chemical substance, adequate ventilation and storage away from incompatible materials are essential to ensure safe usage.

Recent research has also delved into the environmental impact of 2-Propanamine,N,N-bis(1-methylethyl)-. Studies indicate that while it does not readily biodegrade, its persistence in aquatic environments is relatively low. Efforts are ongoing to develop greener synthetic routes that minimize waste generation and reduce environmental footprints. These initiatives align with broader industry trends toward sustainable chemistry practices.

In conclusion,2-Propanamine,N,N-bis(1-methylethyl)- (CAS No. 3424-21-3) is a multifaceted compound with significant implications in synthetic chemistry and pharmaceutical development. Its unique structural features, reactivity patterns, and broad applicability make it an indispensable tool for researchers and industrial chemists alike. As scientific understanding advances, new uses for this compound are likely to emerge, further solidifying its importance in modern chemical science.

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