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Catalog Number:
29855
CAS Number:
51-35-4
trans-L-4-Hydroxyproline, Non-animal origin
Purity:
99.0-101.0% (Assay, dry basis)
Synonym(s):
L-Hyp-OH, (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid, H-Hyp-OH
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Product Information

trans-L-4-Hydroxyproline, a non-animal origin amino acid derivative, is recognized for its unique structural properties that make it an invaluable asset in various applications. This compound is particularly significant in the fields of pharmaceuticals and cosmetics, where it is utilized for its ability to enhance collagen stability and promote skin hydration. Researchers have found that trans-L-4-Hydroxyproline can improve the mechanical properties of collagen-based materials, making it a popular choice in the formulation of anti-aging products and wound healing therapies. Its non-animal origin also appeals to the growing demand for vegan and cruelty-free ingredients in the beauty and health industries.

In addition to its cosmetic applications, trans-L-4-Hydroxyproline is gaining traction in biomedical research, particularly in studies focused on tissue engineering and regenerative medicine. Its role in collagen synthesis and stabilization positions it as a potential candidate for developing innovative treatments for various connective tissue disorders. With its multifunctional benefits and increasing relevance in both cosmetic and medical fields, trans-L-4-Hydroxyproline stands out as a versatile compound that meets the evolving needs of researchers and industry professionals alike.

Synonyms
L-Hyp-OH, (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid, H-Hyp-OH
CAS Number
51-35-4
Purity
99.0-101.0% (Assay, dry basis)
Molecular Formula
C5H9NO3
Molecular Weight
131.1
MDL Number
MFCD00064320
PubChem ID
825
Melting Point
273°C (dec)
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -75 ± 2º (C = 1 in H2O)
Conditions
Store at RT
General Information
Synonyms
L-Hyp-OH, (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid, H-Hyp-OH
CAS Number
51-35-4
Purity
99.0-101.0% (Assay, dry basis)
Molecular Formula
C5H9NO3
Molecular Weight
131.1
MDL Number
MFCD00064320
PubChem ID
825
Melting Point
273°C (dec)
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -75 ± 2º (C = 1 in H2O)
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

trans-L-4-Hydroxyproline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is used in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting collagen-related diseases, enhancing skin health and wound healing.
  • Cosmetic Formulations: Its ability to improve skin elasticity and hydration makes it a popular ingredient in anti-aging creams and serums, providing a natural alternative to synthetic compounds.
  • Food Industry: As a non-animal derived amino acid, it is incorporated into dietary supplements and functional foods aimed at enhancing collagen production, appealing to health-conscious consumers.
  • Biotechnology: Researchers utilize trans-L-4-Hydroxyproline in protein engineering and peptide synthesis, aiding in the development of novel biomaterials with enhanced properties.
  • Research on Fibrosis: It serves as a valuable tool in studies related to fibrosis and tissue repair, helping scientists understand and potentially mitigate scarring and tissue damage.

Citations