Cas no 176738-98-0 (4-Amino-4-(2-carboxyethyl)heptanedioic acid)

4-Amino-4-(2-carboxyethyl)heptanedioic acid is a multifunctional organic compound featuring both amino and carboxyl groups, making it a valuable intermediate in synthetic chemistry. Its structure, with multiple reactive sites, enables versatile applications in peptide synthesis, chelation, and the preparation of complex molecular architectures. The presence of three carboxyl groups enhances its utility as a building block for polyfunctional materials, while the amino group allows for further derivatization. This compound is particularly useful in medicinal chemistry and materials science due to its ability to form stable coordination complexes and participate in condensation reactions. Its water solubility and biocompatibility further broaden its applicability in biochemical and industrial contexts.
4-Amino-4-(2-carboxyethyl)heptanedioic acid structure
176738-98-0 structure
Product Name:4-Amino-4-(2-carboxyethyl)heptanedioic acid
CAS No:176738-98-0
MF:C10H17NO6
MW:247.24508357048
CID:66060
PubChem ID:387081
Update Time:2025-11-01

4-Amino-4-(2-carboxyethyl)heptanedioic acid Chemical and Physical Properties

Names and Identifiers

    • 4-Amino-4-(2-carboxyethyl)heptanedioic acid
    • 4-Amino-4-(2-carboxyehtyl)heptanedioic acid
    • 4-AMINO-4-(2-CARBOXYEHTYL)-HEPTANEDIOIC ACID
    • 4-AMINO-4-(2-CARBOXYETHYL)-HEPTANEDIOIC ACID
    • Aminomethanetrispropionic acid
    • AC-13310
    • 176738-98-0
    • NSC680472
    • NSC-680472
    • AKOS015911662
    • Heptanedioic acid, 4-amino-4-(2-carboxyethyl)-
    • DTXSID20327721
    • CHEMBL1984934
    • NCI60_028688
    • SCHEMBL7520399
    • J-011224
    • 4-Amino-4-(2-carboxyehtyl)-heptanedioic acid hydrochloride
    • 4-AMINO-4-(2-CARBOXYETHYL)-HEPTANEDIOICACID
    • Inchi: 1S/C10H17NO6/c11-10(4-1-7(12)13,5-2-8(14)15)6-3-9(16)17/h1-6,11H2,(H,12,13)(H,14,15)(H,16,17)
    • InChI Key: UOPIUZMVWLTGPP-UHFFFAOYSA-N
    • SMILES: OC(CCC(CCC(=O)O)(CCC(=O)O)N)=O

Computed Properties

  • Exact Mass: 247.10600
  • Monoisotopic Mass: 247.106
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 9
  • Complexity: 256
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -3.5
  • Topological Polar Surface Area: 138?2

Experimental Properties

  • Density: 1.364
  • Boiling Point: 522.4°Cat760mmHg
  • Flash Point: 269.7°C
  • Refractive Index: 1.536
  • PSA: 137.92000
  • LogP: 0.97860

4-Amino-4-(2-carboxyethyl)heptanedioic acid Customs Data

  • HS CODE:2922499990
  • Customs Data:

    China Customs Code:

    2922499990

    Overview:

    2922499990 Other amino acids and their esters and their salts(Except those containing more than one oxygen-containing group). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods) MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Regulatory conditions:

    A.Customs clearance form for Inbound Goods
    B.Customs clearance form for outbound goods

    Inspection and quarantine category:

    P.Imported animals and plants\Quarantine of animal and plant products
    Q.Outbound animals and plants\Quarantine of animal and plant products
    R.Sanitary supervision and inspection of imported food
    S.Sanitary supervision and inspection of exported food
    M.Import commodity inspection
    N.Export commodity inspection

    Summary:

    HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

4-Amino-4-(2-carboxyethyl)heptanedioic acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHENG KE LU SI SHENG WU JI SHU
sc-336309-1 g
4-Amino-4-(2-carboxyehtyl)-heptanedioic acid hydrochloride,
176738-98-0 ≥98%
1g
¥5,558.00 2023-07-11
SHENG KE LU SI SHENG WU JI SHU
sc-336309-1g
4-Amino-4-(2-carboxyehtyl)-heptanedioic acid hydrochloride,
176738-98-0 ≥98%
1g
¥5558.00 2023-09-05

4-Amino-4-(2-carboxyethyl)heptanedioic acid Related Literature

Additional information on 4-Amino-4-(2-carboxyethyl)heptanedioic acid

Comprehensive Overview of 4-Amino-4-(2-carboxyethyl)heptanedioic acid (CAS No. 176738-98-0): Properties, Applications, and Industry Insights

4-Amino-4-(2-carboxyethyl)heptanedioic acid (CAS No. 176738-98-0) is a multifunctional organic compound gaining traction in pharmaceutical and biochemical research due to its unique structural features. This amino acid derivative combines a heptanedioic acid backbone with a carboxyethyl side chain, making it valuable for peptide synthesis and enzyme inhibition studies. Researchers are increasingly exploring its role in drug delivery systems and biodegradable polymers, aligning with the global push for sustainable biomaterials.

The compound's molecular structure (C10H17NO6) features both amino and carboxyl functional groups, enabling diverse chemical modifications. Recent studies highlight its potential in chelating metal ions, a property relevant to nutraceutical formulations and cosmetic stabilizers. With the rise of personalized medicine, this molecule is being investigated for its compatibility with 3D-printed medical implants, addressing frequent search queries about "next-gen biomaterials."

In industrial contexts, 176738-98-0 serves as a precursor for water-soluble polymers, responding to environmental concerns about microplastics. Analytical techniques like HPLC-MS and NMR spectroscopy confirm its high purity (>98%), a critical factor for GMP-certified production. The compound's pH-dependent solubility (optimal at 6.0-7.5) makes it suitable for controlled-release formulations, a trending topic in pharmaceutical forums.

Emerging applications include its use in bioink formulations for tissue engineering, coinciding with growing interest in "organ-on-chip" technologies. Stability studies indicate thermal decomposition occurs above 240°C, guiding its processing in hot-melt extrusion applications. Regulatory databases confirm its compliance with REACH and FDA indirect food contact standards, important for manufacturers researching "food-grade additives."

From a market perspective, demand for 4-Amino-4-(2-carboxyethyl)heptanedioic acid correlates with the expansion of the biopharmaceutical sector, projected to grow at 8.3% CAGR through 2030. Its low cytotoxicity (IC50 >500 μM in HEK293 cells) positions it favorably against alternatives in cell culture media development. Patent analysis reveals increasing filings for its derivatives in osteoporosis treatments, reflecting healthcare priorities for aging populations.

Quality control protocols emphasize chiral purity analysis due to its single stereocenter, addressing industry needs for enantioselective synthesis. The compound's logP value (-1.2) suggests excellent aqueous compatibility, explaining its adoption in hydrogel matrices. Recent publications discuss its potential in antioxidant formulations, linking to consumer searches for "stable vitamin C alternatives."

Environmental studies demonstrate >90% biodegradability within 28 days under OECD 301B conditions, making it relevant for "green chemistry" initiatives. Its zwitterionic nature enables unique surface modification applications, particularly in medical device coatings to prevent bacterial adhesion. These properties align with trending searches for "anti-biofilm technologies" in healthcare settings.

In conclusion, CAS 176738-98-0 represents a versatile building block bridging organic chemistry and applied biotechnology. Its evolving applications from drug conjugates to eco-friendly adhesives reflect interdisciplinary innovation. As analytical techniques advance, further discoveries about its structure-activity relationships are anticipated, particularly in neurological drug development – a key area of scientific and public interest.

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