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Catalog Number:
03154
CAS Number:
3483-82-7
Benzoyl-L-tyrosine ethyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Bz-L-Tyr-OEt
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Product Information

Benzoyl-L-tyrosine ethyl ester is a versatile compound known for its applications in pharmaceuticals and biochemistry. This ester derivative of L-tyrosine features a benzoyl group that enhances its lipophilicity, making it an excellent candidate for drug formulation and delivery systems. Its unique structure allows for improved bioavailability and stability, which are critical factors in the development of effective therapeutic agents. Researchers have utilized Benzoyl-L-tyrosine ethyl ester in the synthesis of various bioactive molecules, particularly in the design of peptide-based drugs and as a building block in organic synthesis.

In addition to its pharmaceutical relevance, this compound is also explored in the field of cosmetic formulations due to its antioxidant properties, which can help protect skin cells from oxidative stress. Its ability to enhance the solubility of active ingredients makes it a valuable component in skincare products. Overall, Benzoyl-L-tyrosine ethyl ester stands out for its multifunctional applications, offering significant advantages in both research and industrial settings.

Synonyms
Bz-L-Tyr-OEt
CAS Number
3483-82-7
Purity
≥ 98% (HPLC)
Molecular Formula
C18H19NO4
Molecular Weight
313.4
MDL Number
MFCD00002388
PubChem ID
253239
Melting Point
119 - 124 °C
Appearance
White to off-white crystal
Optical Rotation
[a]D20 = -28 ± 2 º (C=1 in EtOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Bz-L-Tyr-OEt
CAS Number
3483-82-7
Purity
≥ 98% (HPLC)
Molecular Formula
C18H19NO4
Molecular Weight
313.4
MDL Number
MFCD00002388
PubChem ID
253239
Melting Point
119 - 124 °C
Appearance
White to off-white crystal
Optical Rotation
[a]D20 = -28 ± 2 º (C=1 in EtOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Benzoyl-L-tyrosine ethyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a precursor in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to cross the blood-brain barrier.
  • Cosmetic Formulations: It is incorporated into skincare products for its antioxidant properties, helping to protect the skin from oxidative stress and improve overall skin health.
  • Biochemical Research: Researchers use it as a model compound to study enzyme interactions and protein synthesis, aiding in the understanding of metabolic pathways.
  • Food Industry: The compound is explored for its potential as a natural preservative, offering an alternative to synthetic additives while enhancing flavor profiles.
  • Material Science: It is investigated for its role in developing biodegradable polymers, contributing to more sustainable materials in various applications.

Citations