Description

Allyl 1-(4-Hydroxymethyl-2-Nitrophenyl)-2,3,4-Tri-o-Allyloxycarbonyl-β-D-Glucuronate is a sophisticated, multi-functional chemical intermediate designed for advanced synthetic applications. This compound matters for its role as a key building block in the synthesis of complex molecules, particularly in the development of light-sensitive probes and specialty polymers. It is primarily needed by R&D chemists and process development scientists in the pharmaceutical, agrochemical, and advanced materials industries for creating novel active ingredients and functional materials.

Application

• Photolabile Protecting Group Intermediate: A critical precursor in the synthesis of caged compounds and photoactivatable reagents for biochemical and pharmacological research.
• Specialty Polymer Synthesis: Used in the development of advanced polymers with tailored degradation profiles or light-responsive properties for coatings and biomedical devices.
• Pharmaceutical Intermediate: Serves as a key synthon in the multi-step synthesis of complex drug candidates, particularly those requiring precise spatial and temporal control of activity.
• Agrochemical Research: Employed in the development of novel, targeted agrochemicals where controlled release mechanisms are advantageous.
• Material Science Research: Utilized in creating novel organic materials for optoelectronics and sensor technology due to its nitroaromatic and glucuronate moieties.
• Bioconjugation Chemistry: The allyl and hydroxymethyl groups offer handles for further functionalization and conjugation to biomolecules like proteins or peptides.

Basic Information

Product Name	Allyl 1-(4-Hydroxymethyl-2-Nitrophenyl)-2,3,4-Tri-o-Allyloxycarbonyl-β-D-Glucuronate
CAS No.	1353003-35-6
Molecular Formula	C28H31NO13
Molecular Weight	589.55 g/mol
Synonyms	Allyl 2,3,4-Tri-O-allyloxycarbonyl-1-O-(4-hydroxymethyl-2-nitrophenyl)-β-D-glucopyranuronate; 1-(4-Hydroxymethyl-2-nitrophenyl)-2,3,4-tri-O-(allyloxycarbonyl)-β-D-glucopyranuronic Acid Allyl Ester; β-D-Glucopyranuronic Acid, 1-(4-(hydroxymethyl)-2-nitrophenyl)-2,3,4-tris-O-[(2-propen-1-yloxy)carbonyl]-, 1-(2-propen-1-yl) Ester; Photolabile Glucuronate Intermediate; Nitrophenyl-Glucuronate Allyl Ester; Light-sensitive Glucuronate Synthon.
EINECS	Contact for details

Quality Control

Our production of Allyl 1-(4-Hydroxymethyl-2-Nitrophenyl)-2,3,4-Tri-o-Allyloxycarbonyl-β-D-Glucuronate adheres to stringent quality protocols to ensure batch-to-batch consistency and high purity for research and development. Each lot is characterized using advanced analytical techniques including NMR, HPLC, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to support your regulatory and quality documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is light-sensitive (store away from light) and should be handled under appropriate conditions to prevent decomposition. Keep the container tightly sealed in a dry environment to minimize exposure to moisture.

Specification

Item	Specification
Appearance	Off-white to light yellow solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH guidelines

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