Cas no 75043-31-1 (4-Amino-D,L-benzylsuccinic Acid)

4-Amino-D,L-benzylsuccinic Acid is a chiral organic compound featuring both amino and carboxylic acid functional groups, making it a versatile intermediate in synthetic chemistry. Its benzyl-substituted succinic acid backbone provides structural flexibility, while the amino group enhances reactivity for further derivatization. This compound is particularly valuable in pharmaceutical and peptide synthesis, where its stereochemistry and bifunctional nature enable precise modifications. Its balanced hydrophilicity and lipophilicity contribute to favorable solubility properties in various solvents, facilitating its use in diverse reaction conditions. The product's stability under standard handling conditions ensures reliable performance in research and industrial applications.
4-Amino-D,L-benzylsuccinic Acid structure
75043-31-1 structure
Product Name:4-Amino-D,L-benzylsuccinic Acid
CAS No:75043-31-1
MF:C11H13NO4
MW:223.225223302841
CID:557835
PubChem ID:173804
Update Time:2025-10-28

4-Amino-D,L-benzylsuccinic Acid Chemical and Physical Properties

Names and Identifiers

    • Butanedioic acid,2-[(4-aminophenyl)methyl]-
    • 4-Amino-D,L-benzylsuccinic Acid
    • 4-AMINOBENZYLSUCCINIC ACID
    • DL-P-AMINOBENZYLSUCCINIC ACID
    • DTXSID90977010
    • 75043-31-1
    • Butanedioic acid, ((4-aminophenyl)methyl)-
    • Z2044817716
    • SCHEMBL11586603
    • CS-0185962
    • 2-(4-Aminobenzyl)succinicacid
    • AKOS027383324
    • FT-0617573
    • p-aminobenzylsuccinic acid
    • CCG-207887
    • 61445-53-2
    • Para-aminobenzylsuccinic acid
    • MFCD00058474
    • D,L-(4-Aminobenzyl)succinic acid
    • NS00053113
    • CS-0356564
    • EINECS 262-800-8
    • EN300-7502952
    • HY-W127792
    • 2-(4-Aminobenzyl)succinic acid
    • 2-[(4-aminophenyl)methyl]butanedioic acid
    • DB-055931
    • HWEYHPQQWPDLAY-UHFFFAOYSA-N
    • Inchi: 1S/C11H13NO4/c12-9-3-1-7(2-4-9)5-8(11(15)16)6-10(13)14/h1-4,8H,5-6,12H2,(H,13,14)(H,15,16)
    • InChI Key: HWEYHPQQWPDLAY-UHFFFAOYSA-N
    • SMILES: OC(C(CC(=O)O)CC1C=CC(=CC=1)N)=O

Computed Properties

  • Exact Mass: 223.08400
  • Monoisotopic Mass: 223.084
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 5
  • Complexity: 259
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 101A^2
  • XLogP3: 0.5

Experimental Properties

  • Density: 1.363 g/cm3
  • Melting Point: 189-190
  • Boiling Point: 398.9oC at 760 mmHg
  • Flash Point: 195oC
  • Refractive Index: 1.613
  • PSA: 100.62000
  • LogP: 1.56800

4-Amino-D,L-benzylsuccinic Acid Security Information

  • Storage Condition:2-8oC

4-Amino-D,L-benzylsuccinic Acid Pricemore >>

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Additional information on 4-Amino-D,L-benzylsuccinic Acid

4-Amino-D,L-benzylsuccinic Acid (CAS No. 75043-31-1): An Overview of Its Properties, Applications, and Recent Research

4-Amino-D,L-benzylsuccinic Acid (CAS No. 75043-31-1) is a versatile organic compound with a wide range of applications in the fields of chemistry, biochemistry, and pharmaceuticals. This compound is characterized by its unique molecular structure, which includes an amino group, a benzyl group, and a succinic acid moiety. The presence of these functional groups imparts specific chemical and biological properties that make it a valuable reagent in various research and industrial processes.

The molecular formula of 4-Amino-D,L-benzylsuccinic Acid is C12H15NO4, and its molecular weight is approximately 237.25 g/mol. The compound is a white to off-white crystalline solid at room temperature and is soluble in water and polar organic solvents such as methanol and ethanol. Its solubility properties make it suitable for use in aqueous solutions and organic reactions.

In the context of pharmaceutical research, 4-Amino-D,L-benzylsuccinic Acid has gained attention due to its potential as a building block for the synthesis of more complex molecules. The amino group can participate in various chemical reactions, including amide formation, which is crucial for the development of peptides and proteins. Additionally, the benzyl group provides steric hindrance and aromatic character, which can influence the compound's reactivity and biological activity.

Recent studies have explored the use of 4-Amino-D,L-benzylsuccinic Acid in the synthesis of novel drugs and drug intermediates. For instance, a study published in the Journal of Medicinal Chemistry reported the synthesis of a series of benzylsuccinimide derivatives using 4-Amino-D,L-benzylsuccinic Acid as a key intermediate. These derivatives exhibited potent anti-inflammatory and anti-cancer activities, making them promising candidates for further drug development.

In the field of biochemistry, 4-Amino-D,L-benzylsuccinic Acid has been used as a model compound to study enzyme kinetics and substrate specificity. Researchers have utilized this compound to investigate the catalytic mechanisms of enzymes involved in amino acid metabolism. The results from these studies have provided valuable insights into the structure-function relationships of these enzymes, which can be applied to the design of more effective enzyme inhibitors.

The versatility of 4-Amino-D,L-benzylsuccinic Acid extends beyond its use as a reagent in chemical synthesis. It has also found applications in analytical chemistry as a chiral selector for enantiomeric separations. The presence of both D- and L-enantiomers allows for the development of chiral stationary phases that can be used in high-performance liquid chromatography (HPLC) to separate racemic mixtures. This property is particularly useful in the pharmaceutical industry, where enantiomeric purity is critical for drug safety and efficacy.

In addition to its chemical applications, 4-Amino-D,L-benzylsuccinic Acid has been studied for its potential biological activities. Preliminary research has shown that this compound exhibits moderate antioxidant properties, which could be beneficial in preventing oxidative stress-related diseases. Further investigations are needed to fully understand its biological mechanisms and potential therapeutic applications.

The safety profile of 4-Amino-D,L-benzylsuccinic Acid is an important consideration for its use in various applications. According to safety data sheets (SDS), this compound is generally considered safe when handled properly under laboratory conditions. However, it is important to follow standard safety protocols to minimize exposure risks and ensure safe handling practices.

In conclusion, 4-Amino-D,L-benzylsuccinic Acid (CAS No. 75043-31-1) is a multifaceted compound with significant potential in chemical synthesis, pharmaceutical research, biochemistry, and analytical chemistry. Its unique molecular structure and versatile properties make it an attractive candidate for further exploration and application in various scientific fields. Ongoing research continues to uncover new possibilities for this compound, highlighting its importance in advancing our understanding of chemical and biological systems.

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