4-Nitroaniline-2,3,5,6-D4

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4-Nitroaniline-2,3,5,6-D4 is a remarkable chemical compound that bears a distinctive molecular structure, with four deuterium atoms strategically substituted within its nitroaniline framework. This isotopically labeled molecule plays a crucial role in various scientific applications, particularly in research involving isotope tracing, chemical kinetics, and environmental studies. Its unique isotopic composition provides valuable insights into the behavior and reactions of similar compounds, making it a valuable tool for elucidating complex chemical processes and mechanisms.

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Chemical Properties: 4-Nitroaniline-2,3,5,6-D4


Chemical Name 4-Nitroaniline-2,3,5,6-D4
Alternate Names Aniline Stable Isotopes, Stable Isotopes of Aniline
CAT No. CS-T-59322
CAS Registry# 64164-08-5
Category Stable Isotopes
Stock IN-Stock
Mol. Wt. 142.15 g/mol
Mol. For. C₆H₂D₄N₂O₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Aniline
Smileys [O-][N+](C(C([2H])=C1[2H])=C(C([2H])=C1N)[2H])=O
Canonical Smiles C1=CC(=CC=C1N)[N+](=O)[O-]
InchIKey TYMLOMAKGOJONV-RHQRLBAQSA-N
Inchl InChI=1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2/i1D,2D,3D,4D
IUPAC 2,3,5,6-tetradeuterio-4-nitroaniline
Controlled No
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4-Nitroaniline-2,3,5,6-D4 is a deuterated derivative of 4-nitroaniline, which is a yellow crystalline solid that is primarily used as an intermediate in the production of dyes, pigments, and pharmaceuticals. The deuterated form, 4-Nitroaniline-2,3,5,6-D4, is a labeled compound that has four deuterium atoms substituted for the hydrogen atoms in the molecule, and is used in a variety of research applications. One of the primary uses of 4-Nitroaniline-2,3,5,6-D4 is as a tracer in metabolic studies, where it is used to track the fate of the parent compound in biological systems. This is because the deuterium-labeled compound is chemically identical to the non-labeled compound, but can be distinguished from it using mass spectrometry, allowing for precise measurements of metabolic pathways. In addition to its use as a metabolic tracer, 4-Nitroaniline-2,3,5,6-D4 is also used in analytical chemistry as a standard for quantitative analysis of the non-labeled compound. This is because the deuterium-labeled compound can be accurately measured and used to calibrate analytical instruments. Chemically, 4-Nitroaniline-2,3,5,6-D4 is an aromatic amine that contains a nitro group (-NO2) attached to the aromatic ring. The deuterium atoms in the molecule are all located on the amino group (-NH2), and are chemically equivalent to the hydrogen atoms they replace. The compound is stable under normal conditions, but may be reactive under certain conditions, such as at high temperatures or in the presence of strong acids or bases.

How is 4-Nitroaniline-2,3,5,6-D4 used ?


4-Nitroaniline-2,3,5,6-D4 is primarily used in Pharmaceutical Industry and Drug Discovery.



Synonyms


    • Deuterated 4-Nitroaniline
    • Isotopically Substituted 4-Nitroaniline
    • 2,3,5,6-Tetradeuterio-4-nitroaniline
    • 4-Nitroaniline with Deuterium Substitution
    • Heavy 4-Nitroaniline
    • 4-Nitroaniline-D4
    • 4-Nitroaniline with Deuterium Labeling

Related Compounds

tert-Butyl-d9-amine | Acetophenone D5 | Acetone D6 | Isopropanol D7 | Acetylaniline D5 | Dimethylamine D6 Hydrochloride | Phenyl-D5-boronic acid | Benzaldehyde D5 | Bromocyclopentane D9 | Dibromomethane D2 | Ammoninum D4 Deuteroxide | Aniline D5 | Benzene-d6 | Ethylene-d4 Glycol | Phenol D5 | Benzene D6 D-Atom 99.5% | Deuterium Bromide | Methyl-D3 Amine Hydrochloride | Tert-butyl Alcohol-OD | Methyl Alcohol D4 | Deuterium Chloride | Tert-butanol-d10 | Acetic Acid D4 | Catechol D4 | Chlorobenzene D5 | Trifluoroacetic acid-D | Diethyl Methyl-d3-malonate | tert-Butanol-d9 | Sodium Deuteroxide solution | Phenethylamine D4 HCl | Ethanol-OD | Nitrobenzene D5 | Bromobenzene D5 | Iodomethane-d3 | Sulfuric Acid D2 | Formic Acid-d2 | Benzoic Acid D5 |

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