An internal standard for the quantification of 4-nitrophenylhydrazine
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13C6-4-Nitrophenylhydrazine (hydrochloride)

Item No. 40479

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
(4-nitrophenyl-1,2,3,4,5,6-13C6-4-)hydrazine, monohydrochloride
Synonyms
  • 13C6-4-NPH
  • 13C6-p-Nitrophenylhydrazine
  • 13C6-para-Nitrophenylhydrazine
Molecular Formula
[13C]6H7N3O2 • HCl
Formula Weight
195.6
Purity
≥95%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
Methanol: Soluble
SMILES
NN[13C]1=[13CH][13CH]=[13C]([N+]([O-])=O)[13CH]=[13CH]1.Cl
InChi Code
InChI=1S/C6H7N3O2.ClH/c7-8-5-1-3-6(4-2-5)9(10)11;/h1-4,8H,7H2;1H/i1+1,2+1,3+1,4+1,5+1,6+1;
InChi Key
ZWWXDCOPVYATOQ-BVNCJLROSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Cayman Chemical
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    Product Description

    13C6-4-Nitrophenylhydrazine is intended for use as an internal standard for the quantification of 4-nitrophenylhydrazine by GC- or LC-MS. 13C6-4-Nitrophenylhydrazine is a byproduct in the synthesis of 13C6-3-nitrophenylhydrazine (Item No. 20744). 4-Nitrophenylhydrazine has been used as an intermediate in the synthesis of benzo-indazole derivatives with anti-uterotrophic activity in vivo and pyrazolobenzothiazine derivatives with antiviral activity in vitro.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ragab, M.A., Elagawany, M., Daabees, H., et al. Structure-based design and synthesis of conformationally constrained derivatives of methyl-piperidinopyrazole (MPP) with estrogen receptor (ER) antagonist activity. Bioorg. Chem. 119, 105554 (2022).

    2. Barreca, M.L., Manfroni, G., Leyssen, P., et al. Structure-based discovery of pyrazolobenzothiazine derivatives as inhibitors of hepatitis C virus replication. J. Med. Chem. 56(6), 2270-2282 (2013).