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Sodium 4-Hydroxyphenylglyoxylate CAS NO 54537-30-3


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CAS No.:54537-30-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Sodium 4-Hydroxyphenylglyoxylate is the sodium salt derivative of 4-hydroxymandelic acid, a key synthetic intermediate in organic chemistry. This compound is valued for its role as a versatile building block in the synthesis of more complex molecules, particularly in pharmaceutical and fine chemical manufacturing. Industries such as pharmaceutical R&D, agrochemical production, and specialty chemical synthesis utilize this material for constructing active pharmaceutical ingredients (APIs) and other high-value compounds.

Application

  • Pharmaceutical Intermediate: A crucial precursor in the synthesis of various active pharmaceutical ingredients (APIs), including potential candidates for cardiovascular and neurological therapies.
  • Agrochemical Synthesis: Used as a building block for developing advanced herbicides, fungicides, and plant growth regulators.
  • Fine Chemical Production: Serves as a key starting material for manufacturing dyes, pigments, and performance chemicals.
  • Biochemical Research: Employed in laboratory settings for studying enzyme inhibition and metabolic pathways.
  • Cosmetic Ingredient Synthesis: A potential intermediate for producing certain UV absorbers and skin-conditioning agents.
  • Polymer Modification: Can be used to introduce functional groups into polymer chains for enhanced material properties.

Basic Information

Product Name Sodium 4-Hydroxyphenylglyoxylate
CAS No. 54537-30-3
Molecular Formula C8H5NaO5
Molecular Weight 204.11 g/mol
Synonyms Sodium 4-Hydroxymandelate; 4-Hydroxymandelic Acid Sodium Salt; Sodium (4-Hydroxyphenyl)(oxo)acetate; Sodium α-Oxo-4-hydroxybenzeneacetate; Mandelic acid, 4-hydroxy-, sodium salt; Benzenacetic acid, α-oxo-4-hydroxy-, sodium salt; Sodium 2-hydroxy-2-(4-hydroxyphenyl)acetate (tautomeric form)
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Quality Control

Our Sodium 4-Hydroxyphenylglyoxylate is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, detailing key parameters such as assay, impurity profile, and residual solvents. Our quality commitment aligns with cGMP principles 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 product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. Keep away from incompatible materials such as strong oxidizing agents.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Assay (HPLC) ≥ 98.0%
Loss on Drying ≤ 2.0%
Residue on Ignition ≤ 0.5%
Heavy Metals (as Pb) ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 2.0%
Solubility Soluble in water

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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