Cas no 344298-88-0 (n-Propyl-d7-amine HCl)

n-Propyl-d7-amine HCl is a deuterium-labeled derivative of n-propylamine, where seven hydrogen atoms are replaced with deuterium, enhancing its utility in mass spectrometry and NMR studies. The isotopic labeling ensures minimal interference from background signals, making it ideal for use as an internal standard in quantitative analysis. Its high chemical purity and isotopic enrichment (>98%) guarantee reliable and reproducible results in tracer experiments and metabolic research. The hydrochloride salt form improves stability and solubility in aqueous and organic solvents, facilitating handling in synthetic and analytical applications. This compound is particularly valuable in pharmaceutical and biochemical research for tracking molecular pathways and kinetics with precision.
n-Propyl-d7-amine HCl structure
n-Propyl-d7-amine HCl structure
Product Name:n-Propyl-d7-amine HCl
CAS No:344298-88-0
MF:C3H10ClN
MW:95.5711998939514
CID:304728
PubChem ID:11165
Update Time:2025-10-31

n-Propyl-d7-amine HCl Chemical and Physical Properties

Names and Identifiers

    • 1-Propan-1,1,2,2,3,3,3-d7-amine,hydrochloride (9CI)
    • N-PROPYL-D7-AMINE HCL
    • n-Propyl-D7-amine Cl
    • N-PROPYL-D7-AMINE HYDROCHLORIDE
    • AKOS015950694
    • SY102035
    • 1-Aminopropane hydrochloride
    • PROPYLAMINE HYDROCHLORIDE [MI]
    • NSC210913
    • NSC 210913
    • Propylamine Hydrochloride, >/=98%
    • D74104
    • 1-Propanamine hydrochloride
    • MFCD00012911
    • N-Propylamine HCl
    • A1Z6OVY2HG
    • 1-Propanamine, hydrochloride (1:1)
    • PYNUOAIJIQGACY-UHFFFAOYSA-N
    • Propylamine hydrochloride, >=99%
    • n-Propylammonium chloride
    • n-Propylamine hydrochloride
    • propan-1-amine hydrochloride
    • 1-Propylammonium chloride
    • EINECS 209-129-9
    • FT-0693876
    • Propylammonium chloride
    • SB75356
    • CS-0079898
    • Propylamine, hydrochloride
    • AS-59473
    • Q27273520
    • PROPYLAMINE HYDROCHLORIDE
    • P0522
    • NSC-210913
    • Propan-1-amine;hydrochloride
    • 1-Propanamine, hydrochloride
    • n-PrNH2.HCl
    • UNII-A1Z6OVY2HG
    • DTXSID0060301
    • EN300-55115
    • 344298-88-0
    • 556-53-6
    • A870142
    • n-Propyl-d7-amine HCl
    • Inchi: 1S/C3H9N.ClH/c1-2-3-4;/h2-4H2,1H3;1H
    • InChI Key: PYNUOAIJIQGACY-UHFFFAOYSA-N
    • SMILES: Cl.NCCC

Computed Properties

  • Exact Mass: 102.09400
  • Monoisotopic Mass: 102.094
  • Isotope Atom Count: 7
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 5
  • Rotatable Bond Count: 1
  • Complexity: 7.2
  • 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
  • Topological Polar Surface Area: 26A^2

Experimental Properties

  • PSA: 26.02000
  • LogP: 1.85740

n-Propyl-d7-amine HCl Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
H953789-5mg
n-Propyl-d7-amine HCl
344298-88-0
5mg
$ 64.00 2023-09-07
TRC
H953789-10mg
n-Propyl-d7-amine HCl
344298-88-0
10mg
$ 81.00 2023-09-07
TRC
H953789-50mg
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$144.00 2023-05-18

Additional information on n-Propyl-d7-amine HCl

N-Propyl-d7-amine HCl: A Comprehensive Overview in Modern Chemical and Pharmaceutical Research

The compound with the CAS number 344298-88-0 is known as N-Propyl-d7-amine HCl, a deuterated derivative of N-propylamine that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, characterized by its specific isotopic labeling, finds utility in various applications ranging from analytical chemistry to drug development. The introduction of deuterium atoms (denoted by the suffix "-d7") not only provides a means for isotope labeling but also offers unique advantages in terms of metabolic stability and analytical precision.

In recent years, the demand for isotopically labeled compounds has surged due to their indispensable role in spectroscopic studies, particularly in nuclear magnetic resonance (NMR) spectroscopy. The deuterated version of N-propylamine, N-Propyl-d7-amine HCl, serves as an excellent internal standard or reference compound. Its high purity and stability make it an ideal candidate for complex molecular structure elucidation and dynamic studies. The use of such isotopically labeled compounds enhances the sensitivity and resolution of NMR spectra, enabling researchers to gain deeper insights into the structural and dynamic properties of molecules.

The pharmaceutical industry has also embraced the use of deuterated compounds like N-Propyl-d7-amine HCl for drug development. Deuteration can alter the pharmacokinetic properties of a drug, potentially leading to improved bioavailability, reduced metabolism, and enhanced therapeutic efficacy. For instance, studies have shown that deuterated amine groups can slow down the metabolic degradation of drugs, thereby extending their half-life in the body. This property is particularly valuable in the development of long-acting medications where sustained release is crucial.

Moreover, N-Propyl-d7-amine HCl has found applications in the synthesis of complex organic molecules. Its role as a building block in organic synthesis allows chemists to construct more intricate molecular frameworks with precision. The deuterated atoms provide a unique handle for tracking reaction pathways and intermediates, facilitating the development of novel synthetic strategies. This capability is especially useful in multi-step syntheses where regioselectivity and stereoselectivity are critical.

Recent advancements in mass spectrometry (MS) have further highlighted the importance of isotopically labeled compounds like N-Propyl-d7-amine HCl. Deuterated compounds can be effectively used for quantitative analysis and metabolite identification in biological samples. The distinct mass-to-charge ratio of deuterium allows for clear differentiation between labeled and unlabeled species, enhancing the accuracy and reliability of MS-based analyses. This application is particularly relevant in clinical diagnostics and environmental monitoring, where precise quantification is essential.

The chemical properties of N-Propyl-d7-amine HCl make it a versatile reagent in various chemical transformations. Its amine functionality can participate in nucleophilic substitution reactions, forming new C-N bonds with electrophiles such as acyl chlorides or alkyl halides. Additionally, its deuterated nature provides a means to study reaction kinetics under controlled isotopic conditions, offering valuable insights into reaction mechanisms.

In conclusion, N-Propyl-d7-amine HCl (CAS number 344298-88-0) is a multifaceted compound with significant implications in both academic research and industrial applications. Its role as an NMR standard, drug development aid, synthetic intermediate, and MS analyte underscores its versatility and importance. As research continues to evolve, the utility of isotopically labeled compounds like this one is expected to expand even further, driving innovation across multiple scientific disciplines.

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