4-amino-2,5,3,6-d4-phenol

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4-Amino-2,5,3,6-d4-phenol is a chemically modified compound that bears a striking resemblance to its parent molecule, phenol, yet stands out due to the presence of four deuterium atoms strategically incorporated within its structure. This isotopic substitution imparts unique properties to the compound, making it valuable in various scientific and industrial applications. With its distinctive isotopic signature, 4-amino-2,5,3,6-d4-phenol serves as a versatile tool in research and chemistry, allowing for precise tracing and investigation of reaction pathways and molecular interactions.

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Chemical Properties: 4-amino-2,5,3,6-d4-phenol


Chemical Name 4-amino-2,5,3,6-d4-phenol
CAT No. CS-O-33121
CAS Registry# 70237-44-4
Category Stable Isotopes
Stock IN-Stock
Mol. Wt. 113.15 g/mol
Mol. For. C₆H₃D₄NO
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys NC(C([2H])=C1[2H])=C(C([2H])=C1O)[2H]
Controlled No
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4-amino-2,5,3,6-d4-phenol, also known as 4-amino-2,5,3,6-tetra deuterophenol, is a deuterated derivative of the phenol molecule. It is an organic compound that is used in several applications in the pharmaceutical and chemical industries. This compound is primarily used as a starting material for the synthesis of other organic compounds, including pharmaceuticals and agrochemicals. It is also used as a building block for the preparation of various chemicals, such as dyes, pigments, and polymers. Chemically, 4-amino-2,5,3,6-d4-phenol is a substituted phenol, which means it contains an amino group (-NH2) and a deuterium atom (-D) in addition to the hydroxyl group (-OH) present in the phenol molecule. The presence of deuterium in this compound makes it useful in isotope labeling studies, which can provide insights into chemical reactions and metabolic pathways. In terms of safety, 4-amino-2,5,3,6-d4-phenol is considered to be a low toxicity compound. However, it is still important to handle this compound with care and to follow proper safety protocols when working with it in a laboratory setting. Overall, this compound plays an important role in the synthesis of various organic chemicals and is a valuable tool for researchers in the pharmaceutical and chemical industries.

How is 4-amino-2,5,3,6-d4-phenol used ?


4-amino-2,5,3,6-d4-phenol is primarily used in Pharmaceutical Industry and Drug Discovery.



Synonyms


    • Deuterated 4-aminophenol
    • Isotopically labeled 4-aminophenol
    • 4-Hydroxy-2,5,3,6-tetra-deuterophenylamine
    • Deuterium-substituted 4-aminophenol
    • 4-Amino-2,5,3,6-dideuterophenol
    • D4-4-aminophenol
    • Isotope-tagged 4-aminophenol

Related Compounds

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

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