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Girard's Reagent T
[CAS# 123-46-6]

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Identification
Classification Catalysts and additives
Name Girard's Reagent T
Synonyms (Carboxymethyl)trimethylammonium chloride hydrazide; 2-Hydrazino-N,N,N-trimethyl-2-oxo-ethanaminium chloride
Molecular Structure CAS # 123-46-6, Girard's Reagent T, (Carboxymethyl)trimethylammonium chloride hydrazide, 2-Hydrazino-N,N,N-trimethyl-2-oxo-ethanaminium chloride
Molecular Formula C5H14N3O.Cl
Molecular Weight 167.64
CAS Registry Number 123-46-6
EC Number 204-629-3
SMILES C[N+](C)(C)CC(=O)NN.[Cl-]
Properties
Melting point 188-192 ºC
Water solubility soluble
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
Girard's Reagent T, chemically known as 2,4-dinitrophenylhydrazine hydrochloride, is a specialized reagent used primarily for the detection and identification of carbonyl compounds, such as aldehydes and ketones. The discovery of Girard's Reagent T dates back to the mid-20th century when it was developed by the chemist Henri Girard. Girard's innovative approach aimed to create a selective reagent that could facilitate the analysis of carbonyl functionalities in organic compounds, thus enhancing the efficiency of chemical analysis in laboratories.

The structure of Girard's Reagent T features a hydrazine moiety that is particularly reactive toward carbonyl groups. When a carbonyl compound reacts with Girard's Reagent T, it forms a stable hydrazone derivative. This reaction not only helps in the identification of the carbonyl compound but also enhances its stability for subsequent analysis. The formation of these derivatives allows for easier purification and characterization of the target compounds through various techniques such as chromatography and spectrometry.

Girard's Reagent T is widely utilized in organic synthesis and analytical chemistry. One of its primary applications is in the qualitative and quantitative analysis of aldehydes and ketones in complex mixtures. For instance, in environmental chemistry, it is often employed to detect carbonyl pollutants in air and water samples. The reagent’s ability to form colored derivatives with carbonyls allows for straightforward visual or spectrophotometric determination of these compounds, making it a valuable tool in environmental monitoring.

Moreover, Girard's Reagent T plays a significant role in the pharmaceutical industry, where it is used in the synthesis and characterization of various drug intermediates. The formation of hydrazone derivatives can aid in purifying active pharmaceutical ingredients (APIs) by facilitating their separation from reaction mixtures. Additionally, the stability of these derivatives enhances the handling and storage of reactive carbonyl-containing compounds, which are otherwise prone to decomposition.

In recent years, the applications of Girard's Reagent T have expanded into proteomics and biomolecular research. It has been utilized for the labeling of carbonyl groups in proteins, which can help in studying post-translational modifications and protein interactions. This capability is particularly useful in understanding the biochemical pathways involved in various diseases, as it allows researchers to track changes in protein structure and function.

Furthermore, ongoing research continues to explore the potential of Girard's Reagent T in new areas, such as drug discovery and nanotechnology. Its unique reactivity toward carbonyl compounds positions it as a potential candidate for developing targeted delivery systems or novel therapeutic agents.

In conclusion, Girard's Reagent T is a crucial chemical reagent with extensive applications in analytical chemistry, organic synthesis, and biochemistry. Its ability to selectively react with carbonyl compounds has made it an invaluable tool in various scientific fields, from environmental analysis to pharmaceutical development. The continued exploration of its properties and applications is likely to yield new insights and innovations in chemical research.
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