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Catalog Number:
37533
CAS Number:
870991-68-7
1S,2S-1,2-Bis(2-hydroxyphenyl)ethylenediamine
Purity:
≥ 97% (T)(HPLC)
Synonym(s):
(1S,2S-1,2-Diamino-1,2-bis(2-hydroxyphenyl)ethane, 2,2'-[(1S,2S-1,2-Diaminoethylene]bisphenol
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Product Information

(1S,2S)-1,2-Bis(2-hydroxyphenyl)ethylenediamine is a versatile compound recognized for its unique chelating properties, making it particularly valuable in various industrial and research applications. This compound, also known as bis(2-hydroxyphenyl)ethylenediamine, is primarily utilized in the synthesis of advanced materials and as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions enhances its utility in catalysis and material science, particularly in the development of novel catalysts for organic reactions and in the formulation of high-performance polymers.

Researchers and industry professionals appreciate this compound for its effectiveness in stabilizing metal ions, which can lead to improved efficiency in catalytic processes. Additionally, its antioxidant properties make it a candidate for applications in pharmaceuticals and cosmetics, where it can help protect formulations from oxidative degradation. The compound's dual functionality as both a ligand and an antioxidant positions it as a valuable tool in various fields, including organic synthesis, materials science, and biochemistry.

Synonyms
(1S,2S-1,2-Diamino-1,2-bis(2-hydroxyphenyl)ethane, 2,2'-[(1S,2S-1,2-Diaminoethylene]bisphenol
CAS Number
870991-68-7
Purity
≥ 97% (T)(HPLC)
Molecular Formula
C14H16N2O2
Molecular Weight
244.29
PubChem ID
164408
Melting Point
159 °C (dec.)
Appearance
White to Light yellow to Light orange pow
Optical Rotation
[α]20D = -64 to -68 ° (C=1, CHCl3)
Conditions
Store at RT
General Information
Synonyms
(1S,2S-1,2-Diamino-1,2-bis(2-hydroxyphenyl)ethane, 2,2'-[(1S,2S-1,2-Diaminoethylene]bisphenol
CAS Number
870991-68-7
Purity
≥ 97% (T)(HPLC)
Molecular Formula
C14H16N2O2
Molecular Weight
244.29
PubChem ID
164408
Melting Point
159 °C (dec.)
Appearance
White to Light yellow to Light orange pow
Optical Rotation
[α]20D = -64 to -68 ° (C=1, CHCl3)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(1S,2S)-1,2-Bis(2-hydroxyphenyl)ethylenediamine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chemical Synthesis: It is used as a ligand in coordination chemistry, facilitating the formation of metal complexes that are essential for catalysis in organic reactions.
  • Analytical Chemistry: The compound acts as a reagent in analytical methods, enhancing the detection of specific analytes in complex mixtures, which is crucial in quality control processes.
  • Biochemical Research: It plays a role in studying enzyme interactions and mechanisms, providing insights into biochemical pathways that can lead to new therapeutic targets.
  • Material Science: This chemical is explored for its potential in developing advanced materials, such as polymers with enhanced thermal and mechanical properties, benefiting industries like aerospace and automotive.

Citations