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Catalog Number:
24590
CAS Number:
611-71-2
Ácido R -(-)-mandélico
Purity:
≥ 99,75 % (HPLC, pureza quiral)
Synonym(s):
Ácido (R)-α-hidroxifenilacético
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Product Information

(R)-(-)-Mandelic acid is a versatile organic compound known for its unique properties and applications in various fields. This chiral molecule, characterized by its hydroxyl and carboxylic acid functional groups, is widely recognized for its role in the pharmaceutical industry, particularly in the synthesis of optically active intermediates. Its ability to act as a chiral building block makes it invaluable in the production of enantiomerically pure drugs, enhancing the efficacy and safety profiles of pharmaceutical formulations. Additionally, (R)-(-)-Mandelic acid is utilized in cosmetic formulations due to its gentle exfoliating properties, promoting skin renewal and improving overall texture.

Researchers and industry professionals appreciate (R)-(-)-Mandelic acid for its low toxicity and biocompatibility, making it suitable for various applications, including the development of antimicrobial agents and as a potential treatment for urinary tract infections. Its unique features, such as its ability to inhibit bacterial growth, further underscore its relevance in both medicinal and cosmetic applications. With its broad range of uses and benefits, (R)-(-)-Mandelic acid stands out as a crucial compound for innovation in the chemical and pharmaceutical sectors.

Synonyms
Ácido (R)-α-hidroxifenilacético
CAS Number
611-71-2
Purity
≥ 99,75 % (HPLC, pureza quiral)
Molecular Formula
C8H8O3
Molecular Weight
152.15
MDL Number
MFCD00064251
PubChem ID
1292
Melting Point
131-134 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 30 : ≥ -148,5º (C=2 en H 2 O)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido (R)-α-hidroxifenilacético
CAS Number
611-71-2
Purity
≥ 99,75 % (HPLC, pureza quiral)
Molecular Formula
C8H8O3
Molecular Weight
152.15
MDL Number
MFCD00064251
PubChem ID
1292
Melting Point
131-134 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 30 : ≥ -148,5º (C=2 en H 2 O)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-(-)-Mandelic acid is widely utilized in research focused on

  • Pharmaceutical Development: It serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of antibiotics and anti-inflammatory drugs.
  • Cosmetic Formulations: This compound is often incorporated into skincare products for its gentle exfoliating properties, helping to improve skin texture and reduce acne.
  • Analytical Chemistry: Used as a chiral resolving agent, it aids in the separation of enantiomers in complex mixtures, which is crucial for quality control in drug manufacturing.
  • Food Industry: It acts as a flavoring agent and preservative, contributing to the stability and taste of various food products.
  • Biotechnology: Its role in biocatalysis is significant, as it can enhance the efficiency of enzymatic reactions, making it valuable in the production of fine chemicals.

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