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Available Variants500 g
CHA.56821-500g
Price
€148.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 g | CHA.56821-500g | €148.00 |
ChiPros®, produced by BASF, 99%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | C6H5CH(OH)CO2H |
|---|---|
| CAS Number | 611-71-2 |
| Molecular Weight | 152.15 |
| UNSPSC Code | 12352106 |
| NACRES | NA.22 |
| PubChem Substance ID | 329764292 |
| EC Number | 210-276-6 |
| Beilstein/REAXYS Number | 2691094 |
| MDL number | MFCD00064251 |
| Assay | ≥98.5%, 99% |
| Form | crystals |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H318 |
| pcodes | P280 - P305 + P351 + P338 |
| Hazard Classifications | Eye Dam. 1 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 1 |
| flash_point_f | >374.0 °F |
| flash_point_c | > 190 °C |
Technical Overview & Applications Use-case context
(R)-(−)-Mandelic acid, with the CAS number 611-71-2, is a naturally occurring organic compound that belongs to the family of alpha-hydroxy acids. It is an optically active compound, existing as a single enantiomer, and is commonly used as a resolving agent in the separation of racemic mixtures. (R)-(−)-Mandelic acid is also utilized as a precursor in the synthesis of various pharmaceuticals and fine chemicals, taking advantage of its chiral center to introduce asymmetry into target molecules. The compounds unique properties make it a valuable tool in asymmetric synthesis, and its applications continue to expand in the fields of medicinal chemistry and chemical synthesis. Additionally, (R)-(−)-Mandelic acid has been investigated for its potential antibacterial and antifungal activities, further highlighting its versatility and potential uses.
