Description

(1,1-Dioxothiomorpholino)Acetic Acid Monohydrate is a high-purity, specialized organic compound featuring a thiomorpholine dioxide moiety. This compound is valued as a crucial building block and intermediate in advanced synthetic chemistry, particularly for the development of novel active pharmaceutical ingredients (APIs). It is primarily sought by pharmaceutical research and development organizations and fine chemical manufacturers engaged in the synthesis of complex molecules.

Application

• Pharmaceutical Intermediate: Key synthetic precursor in the research and production of new drug candidates, particularly those targeting neurological and metabolic pathways.
• Organic Synthesis Building Block: Utilized in the construction of complex molecular architectures due to its reactive carboxylic acid and heterocyclic functionalities.
• Ligand and Catalyst Development: Serves as a starting material for creating novel ligands used in asymmetric catalysis and metal complexation.
• Bioconjugation Chemistry: Potential use in developing linkers for antibody-drug conjugates (ADCs) or other bioconjugation applications.
• Agrochemical Research: Intermediate in the synthesis of novel herbicides, fungicides, or plant growth regulators.
• Material Science Research: Used in the development of specialty polymers or functional materials with specific chemical properties.

Basic Information

Product Name	(1,1-Dioxothiomorpholino)Acetic Acid Monohydrate
CAS No.	155480-08-3
Molecular Formula	C6H11NO5S
Molecular Weight	209.22 g/mol
Synonyms	2-(1,1-Dioxo-1,4-thiomorpholin-4-yl)acetic acid monohydrate; Thiomorpholine-1,1-dioxide-4-acetic acid hydrate; 4-Carboxymethylthiomorpholine 1,1-dioxide monohydrate; (Thiomorpholino-1,1-dioxide-4-yl)acetic acid hydrate; Acetic acid, 2-(1,1-dioxido-4-thiomorpholinyl)-, monohydrate; 155480-08-3; (1,1-Dioxothiomorpholin-4-yl)acetic acid monohydrate
EINECS	Contact for details

Quality Control

Our (1,1-Dioxothiomorpholino)Acetic Acid Monohydrate is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with each shipment, which includes results from HPLC, NMR, and other relevant spectroscopic and chromatographic methods. Our quality commitment aligns with cGMP principles where applicable for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); ensure containers are kept sealed to prevent absorption of atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Water Content (KF)	7.0 - 9.0% (Theoretical for monohydrate: ~8.6%)
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.