Description

Rivipansel Sodium is a high-purity, investigational pharmaceutical compound with significant therapeutic potential. This compound is a glycomimetic drug candidate designed to target specific inflammatory pathways. It is primarily of interest to pharmaceutical R&D departments, contract research organizations (CROs), and manufacturers developing novel treatments for acute and chronic inflammatory conditions. The material is supplied under strict quality control to support pre-clinical and clinical development programs.

Application

• Pharmaceutical Research & Development (R&D): Serves as a key active pharmaceutical ingredient (API) or reference standard in the development of novel anti-inflammatory therapeutics.
• Pre-clinical Studies: Used in in vitro and in vivo studies to investigate efficacy, pharmacokinetics, and mechanism of action for conditions like ischemia-reperfusion injury.
• Clinical Trial Material (CTM) Manufacturing: Supplied as a GMP-grade intermediate for the production of drug products intended for Phase I-III clinical trials.
• Analytical Reference Standard: Provides a high-purity benchmark for method development, validation, and quality control testing in analytical laboratories.
• Biochemical Research: Used as a tool compound to study selectin-mediated cell adhesion and signaling processes in immunological research.

Basic Information

Product Name	Rivipansel Sodium
CAS No.	927881-99-0
Molecular Formula	C20H30NNaO15S2
Molecular Weight	619.57 g/mol
Synonyms	GMI-1070; Rivipansel; Sodium Rivipansel; (2S,3S,4R,5S,6R)-6-[[(2S,3R,4R,5R,6R)-3-Acetamido-5-[(2S,3S,4R,5R)-4,5-dihydroxy-3-[(1R,2R)-1,2,3-trihydroxypropyl]oxolan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-hydroxy-5-(2-sulfoethylamino)-2-(sulfomethyl)oxane-3-carboxylic acid sodium salt
EINECS	Contact for details

Quality Control

Our Rivipansel Sodium is manufactured and tested under a quality management system to ensure batch-to-batch consistency and reliability for critical research applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We can supply material suitable for research use (RUO) or under more stringent controls aligned with GMP guidelines for pre-clinical and clinical development. Specifications are designed to meet the rigorous demands of pharmaceutical development.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider desiccated conditions.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Water Content (KF)	≤5.0%
Residue on Ignition	≤1.0%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Individual impurity ≤0.5%; Total impurities ≤2.0%
Bacterial Endotoxins	<1.0 EU/mg (if applicable)

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