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  • 1224048-26-3 Structure
  • Basic information

    1. Product Name: ala-NTBC
    2. Synonyms:
    3. CAS NO:1224048-26-3
    4. Molecular Formula:
    5. Molecular Weight: 400.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1224048-26-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ala-NTBC(CAS DataBase Reference)
    10. NIST Chemistry Reference: ala-NTBC(1224048-26-3)
    11. EPA Substance Registry System: ala-NTBC(1224048-26-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1224048-26-3(Hazardous Substances Data)

1224048-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224048-26-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,0,4 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1224048-26:
(9*1)+(8*2)+(7*2)+(6*4)+(5*0)+(4*4)+(3*8)+(2*2)+(1*6)=113
113 % 10 = 3
So 1224048-26-3 is a valid CAS Registry Number.

1224048-26-3Upstream product

1224048-26-3Downstream Products

1224048-26-3Relevant articles and documents

Identification of NTBC metabolites in urine from patients with hereditary tyrosinemia type 1 using two different mass spectrometric platforms: Triple stage quadrupole and LTQ-Orbitrap

Herebian, Diran,Lamshoeft, Marc,Mayatepek, Ertan,Spiekerkoetter, Ute

, p. 791 - 800 (2010)

The objective of our work was to identify known and unknown metabolites of the drug NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione) in urine from patients during the treatment of hereditary tyrosinemia type 1 (HT-1) disease, a severe inborn error of tyrosine metabolism. Two different mass spectrometric techniques, a triple stage quadrupole and an LTQ-Orbitrap (Fourier transform mass spectrometry (FTMS)), were used for the identification and the structural elucidation of the detected metabolites. Initially, the mass spectrometric (MS) approach consisted of the precursor ion scan detection of the selected product ions, followed by the corresponding collision-induced dissociation (CID) fragmentation analysis (MS2) for the targeted selected reaction monitoring (SRM) mode. Subsequently, accurate and high-resolution full scan and MS/MS measurements were performed on the possible metabolites using the LTQ-Orbitrap. Final confirmation of the identified metabolites was achieved by measuring commercially supplied or laboratory-synthesized standards. Altogether six metabolites, including NTBC itself, were extracted, detected and identified. In addition, two new NTBC metabolites were unambiguously identified as amino acid conjugates, namely glycine-NTBC and b-alanine-NTBC. These identifications were based on their characteristics of chromatographic retention times, protonated molecular ions, elemental compositions, product ions (using CID and higher-energy C-trap dissociation (HCD) techniques) and synthesized references. The applied MS strategy, based on two different MS platforms (LC/MS/MS and FTMS), allowed the rapid identification analysis of the drug metabolites from human extracts and could be used for pharmaceutical research and drug development.

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