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Catalog Number:
31341
CAS Number:
31938-11-1
O-Tritylhydroxylamine
Purity:
≥ 99% (HPLC)
Synonym(s):
O-(Triphenylmethyl)hydroxylamine
Documents
$65.40 /1G
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Product Information

O-Tritylhydroxylamine is a versatile chemical compound widely recognized for its utility in organic synthesis and pharmaceutical applications. This compound serves as a valuable reagent in the preparation of amines and can be utilized in the synthesis of various nitrogen-containing compounds. Its unique trityl protecting group enhances stability and solubility, making it an ideal choice for researchers looking to streamline their synthetic pathways. O-Tritylhydroxylamine is particularly beneficial in the development of pharmaceuticals, agrochemicals, and fine chemicals, where precision and efficiency are paramount.

In addition to its role in synthesis, O-Tritylhydroxylamine is also employed in the field of analytical chemistry, where it can aid in the detection and quantification of specific compounds. Its ability to form stable derivatives allows for improved analytical performance, making it a preferred choice among chemists. With its broad range of applications and notable advantages over similar compounds, O-Tritylhydroxylamine stands out as a crucial tool for professionals in the chemical and pharmaceutical industries.

Synonyms
O-(Triphenylmethyl)hydroxylamine
CAS Number
31938-11-1
Purity
≥ 99% (HPLC)
Molecular Formula
C19H17NO
Molecular Weight
275.34
MDL Number
MFCD00042818
PubChem ID
3015602
Melting Point
83-88 °C
Appearance
White crystal
Conditions
Store at 2-8 °C
General Information
Synonyms
O-(Triphenylmethyl)hydroxylamine
CAS Number
31938-11-1
Purity
≥ 99% (HPLC)
Molecular Formula
C19H17NO
Molecular Weight
275.34
MDL Number
MFCD00042818
PubChem ID
3015602
Melting Point
83-88 °C
Appearance
White crystal
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

O-Tritylhydroxylamine is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly for the synthesis of amines and other nitrogen-containing compounds, making it invaluable for chemists developing new pharmaceuticals.
  • Protecting Group Strategy: It acts as a protecting group for hydroxylamine, allowing chemists to selectively modify other functional groups without affecting the amine, which is crucial in complex organic synthesis.
  • Analytical Chemistry: O-Tritylhydroxylamine is used in the derivatization of carbonyl compounds, enhancing their detection and quantification in various analytical techniques, including chromatography.
  • Biochemical Applications: In biochemistry, it is employed to modify biomolecules, aiding in the study of enzyme mechanisms and interactions, which is essential for drug discovery and development.
  • Material Science: This compound is also explored in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties that enhance material performance.

Citations