{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "codes": [
        {
          "uuid": "9fca830e-e420-43d7-a0e7-cecbd0132cf9",
          "code": "58200-64-9",
          "type": "PRIMARY",
          "url": "https://commonchemistry.cas.org/detail?cas_rn=58200-64-9",
          "code_system": "CAS",
          "references": [
            "153f1d77-f5fc-43dc-90c9-27d0ad9ddf80",
            "cc8ff2b7-dc22-42fc-a49c-4a7912703490"
          ]
        },
        {
          "uuid": "a8b16c70-2bcd-4ad3-824b-5e78ea9c48ba",
          "code": "91864449",
          "type": "PRIMARY",
          "url": "https://pubchem.ncbi.nlm.nih.gov/compound/91864449",
          "code_system": "PUBCHEM",
          "references": [
            "153f1d77-f5fc-43dc-90c9-27d0ad9ddf80"
          ]
        },
        {
          "uuid": "c832eca9-fc6a-46b1-8c92-69a8b99bc26d",
          "code": "3H9QKO17ON",
          "type": "PRIMARY",
          "code_system": "FDA UNII"
        }
      ],
      "substance_class": "chemical",
      "names": [
        {
          "uuid": "f0032392-afb1-43f8-84e3-92485cb876ab",
          "name": "1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, 1,2,3-TRIS(2-HEXYLDECYL) ESTER",
          "stdName": "1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, 1,2,3-TRIS(2-HEXYLDECYL) ESTER",
          "type": "sys",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "be6fcc45-b717-459a-a765-a9372442e06c",
            "71b35dbd-e7da-40e9-824d-dfa0c036db31"
          ],
          "display_name": false
        },
        {
          "uuid": "8c412598-3e47-42b2-bcae-c2e9a29e07b1",
          "name": "TRIHEXYLDECYL CITRATE",
          "stdName": "TRIHEXYLDECYL CITRATE",
          "type": "of",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "b7c4e882-7881-4bd5-ae4e-cafeecaad71f",
            "be6fcc45-b717-459a-a765-a9372442e06c",
            "97119423-e24e-410b-8847-3350f1687ffc",
            "71b35dbd-e7da-40e9-824d-dfa0c036db31"
          ],
          "display_name": true,
          "domains": [
            "cosmetic"
          ],
          "name_orgs": [
            {
              "uuid": "2eaed272-1794-448e-ad55-9a7cd703a177",
              "name_org": "INCI"
            }
          ]
        }
      ],
      "references": [
        {
          "uuid": "b7c4e882-7881-4bd5-ae4e-cafeecaad71f",
          "citation": "pcpc",
          "doc_type": "SRS",
          "public_domain": true,
          "tags": [
            "NOMEN",
            "PUBLIC_DOMAIN_RELEASE",
            "AUTO_SELECTED"
          ]
        },
        {
          "uuid": "71b35dbd-e7da-40e9-824d-dfa0c036db31",
          "citation": "PERSONAL CARE PRODUCTS COUNCIL",
          "doc_type": "PERSONAL CARE PRODUCTS COUNCIL",
          "public_domain": true,
          "tags": [
            "NOMEN"
          ]
        },
        {
          "uuid": "be6fcc45-b717-459a-a765-a9372442e06c",
          "citation": "STN",
          "doc_type": "SRS",
          "public_domain": true,
          "tags": [
            "NOMEN"
          ]
        },
        {
          "uuid": "153f1d77-f5fc-43dc-90c9-27d0ad9ddf80",
          "citation": "SRS CODE IMPORT",
          "doc_type": "SRS",
          "public_domain": true,
          "document_date": 1493393004000,
          "tags": [
            "NOMEN"
          ]
        },
        {
          "uuid": "25e4d1d5-f985-45e8-8266-34a464156b0f",
          "citation": "SRS import [3H9QKO17ON]",
          "url": "http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=3H9QKO17ON",
          "doc_type": "SRS",
          "public_domain": true,
          "document_date": 1493393004000,
          "tags": [
            "NOMEN"
          ]
        },
        {
          "uuid": "97119423-e24e-410b-8847-3350f1687ffc",
          "citation": "TRIHEXYLDECYL CITRATE [INCI]",
          "doc_type": "SRS_LOCATOR",
          "public_domain": true
        },
        {
          "uuid": "cc8ff2b7-dc22-42fc-a49c-4a7912703490",
          "citation": "STN",
          "doc_type": "STN (SCIFINDER)",
          "public_domain": true
        }
      ],
      "definition_type": "PRIMARY",
      "moieties": [
        {
          "uuid": "10ef46e2-299c-4744-b652-4187efc3789c",
          "id": "10ef46e2-299c-4744-b652-4187efc3789c",
          "molfile": "\n  Marvin  01132101062D          \n\n 61 60  0  0  0  0            999 V2000\n   16.7900  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0742  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3582  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6469  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9309  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2151  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4991  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7831  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  3  0  0\n   11.0674  -11.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7727  -12.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7727  -13.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -13.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -14.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7727  -14.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3560  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6401  -11.1278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241   -9.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2083  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4923  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4923  -11.5402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7763  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0605  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0605   -9.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3445  -11.1278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6332  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  3  0  0\n    3.9172  -11.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2119  -12.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2119  -13.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -13.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -14.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2119  -14.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2014  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4855  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7695  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0559  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.3377  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.3736  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.0896  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8054  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4923   -9.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7763   -9.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2083   -9.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2083   -8.6482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  3  0  0\n    9.6295   -8.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3349   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0403   -8.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7457   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4511   -8.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1565   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241   -7.4108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6401   -6.9983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6401   -6.1733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3560   -5.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3560   -4.9312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674   -4.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674   -3.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7831   -3.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  2  1  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  1  0  0  0  0\n  6  5  1  0  0  0  0\n  7  6  1  0  0  0  0\n  8  7  1  0  0  0  0\n  9  8  1  0  0  0  0\n  9 10  1  0  0  0  0\n 16  9  1  0  0  0  0\n 10 11  1  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  1  0  0  0  0\n 13 14  1  0  0  0  0\n 14 15  1  0  0  0  0\n 17 16  1  0  0  0  0\n 18 17  1  0  0  0  0\n 18 19  2  0  0  0  0\n 20 18  1  0  0  0  0\n 21 20  1  0  0  0  0\n 21 22  1  0  0  0  0\n 23 21  1  0  0  0  0\n 21 43  1  0  0  0  0\n 24 23  1  0  0  0  0\n 24 25  2  0  0  0  0\n 24 26  1  0  0  0  0\n 26 27  1  0  0  0  0\n 27 28  1  0  0  0  0\n 28 29  1  0  0  0  0\n 28 35  1  0  0  0  0\n 29 30  1  0  0  0  0\n 30 31  1  0  0  0  0\n 31 32  1  0  0  0  0\n 32 33  1  0  0  0  0\n 33 34  1  0  0  0  0\n 35 36  1  0  0  0  0\n 36 37  1  0  0  0  0\n 37 38  1  0  0  0  0\n 38 39  1  0  0  0  0\n 39 40  1  0  0  0  0\n 40 41  1  0  0  0  0\n 41 42  1  0  0  0  0\n 43 44  2  0  0  0  0\n 43 45  1  0  0  0  0\n 45 46  1  0  0  0  0\n 46 47  1  0  0  0  0\n 47 48  1  0  0  0  0\n 47 54  1  0  0  0  0\n 48 49  1  0  0  0  0\n 49 50  1  0  0  0  0\n 50 51  1  0  0  0  0\n 51 52  1  0  0  0  0\n 52 53  1  0  0  0  0\n 54 55  1  0  0  0  0\n 55 56  1  0  0  0  0\n 56 57  1  0  0  0  0\n 57 58  1  0  0  0  0\n 58 59  1  0  0  0  0\n 59 60  1  0  0  0  0\n 60 61  1  0  0  0  0\nM  END",
          "smiles": "CCCCCCCCC(CCCCCC)COC(=O)CC(CC(=O)OCC(CCCCCC)CCCCCCCC)(C(=O)OCC(CCCCCC)CCCCCCCC)O",
          "formula": "C54H104O7",
          "atropisomerism": "No",
          "charge": 0,
          "count": 1,
          "stereochemistry": "MIXED",
          "count_amount": {
            "type": "MOL RATIO",
            "average": 1,
            "units": "MOL RATIO",
            "uuid": "d6392c0f-d110-41d9-9366-7073ef84a3ed"
          },
          "defined_stereo": 0,
          "ez_centers": 0,
          "molecular_weight": "865.4014",
          "optical_activity": "UNSPECIFIED",
          "stereo_centers": 3
        }
      ],
      "definition_level": "COMPLETE",
      "uuid": "3a3be73e-faaf-4cd2-a103-f667afea3915",
      "version": "3",
      "structure": {
        "id": "452ecd5c-f044-4b16-990c-990a9fd5f12c",
        "molfile": "\n  Marvin  01132103382D          \n\n 61 60  0  0  0  0            999 V2000\n    6.0605  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7763  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4923  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4923  -11.5402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4923   -9.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7763   -9.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2083   -9.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2083   -8.6482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241   -7.4108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6401   -6.9983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6401   -6.1733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3560   -5.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3560   -4.9312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674   -4.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674   -3.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7831   -3.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6295   -8.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3349   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0403   -8.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7457   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4511   -8.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1565   -8.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2083  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9241   -9.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6401  -11.1278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3560  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7831  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4991  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2151  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9309  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6469  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3582  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0742  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7900  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -11.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7727  -12.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7727  -13.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -13.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0674  -14.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7727  -14.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0605   -9.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3445  -11.1278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6332  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2014  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4855  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7695  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0559  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.3377  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.3736  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.0896  -10.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8054  -11.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -11.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2119  -12.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2119  -13.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -13.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9172  -14.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2119  -14.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  5  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  1  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  1  0  0  0  0\n 13 14  1  0  0  0  0\n 14 15  1  0  0  0  0\n 15 16  1  0  0  0  0\n 16 17  1  0  0  0  0\n  9 18  1  0  0  0  0\n 18 19  1  0  0  0  0\n 19 20  1  0  0  0  0\n 20 21  1  0  0  0  0\n 21 22  1  0  0  0  0\n 22 23  1  0  0  0  0\n  3 24  1  0  0  0  0\n 24 25  1  0  0  0  0\n 25 26  2  0  0  0  0\n 25 27  1  0  0  0  0\n 27 28  1  0  0  0  0\n 28 29  1  0  0  0  0\n 29 30  1  0  0  0  0\n 30 31  1  0  0  0  0\n 31 32  1  0  0  0  0\n 32 33  1  0  0  0  0\n 33 34  1  0  0  0  0\n 34 35  1  0  0  0  0\n 35 36  1  0  0  0  0\n 36 37  1  0  0  0  0\n 29 38  1  0  0  0  0\n 38 39  1  0  0  0  0\n 39 40  1  0  0  0  0\n 40 41  1  0  0  0  0\n 41 42  1  0  0  0  0\n 42 43  1  0  0  0  0\n  1 44  2  0  0  0  0\n  1 45  1  0  0  0  0\n 45 46  1  0  0  0  0\n 46 47  1  0  0  0  0\n 47 48  1  0  0  0  0\n 48 49  1  0  0  0  0\n 49 50  1  0  0  0  0\n 50 51  1  0  0  0  0\n 51 52  1  0  0  0  0\n 52 53  1  0  0  0  0\n 53 54  1  0  0  0  0\n 54 55  1  0  0  0  0\n 47 56  1  0  0  0  0\n 56 57  1  0  0  0  0\n 57 58  1  0  0  0  0\n 58 59  1  0  0  0  0\n 59 60  1  0  0  0  0\n 60 61  1  0  0  0  0\nM  END",
        "smiles": "CCCCCCCCC(CCCCCC)COC(=O)CC(CC(=O)OCC(CCCCCC)CCCCCCCC)(C(=O)OCC(CCCCCC)CCCCCCCC)O",
        "formula": "C54H104O7",
        "atropisomerism": "No",
        "charge": 0,
        "count": 1,
        "stereochemistry": "MIXED",
        "defined_stereo": 0,
        "ez_centers": 0,
        "molecular_weight": "865.4014",
        "optical_activity": "UNSPECIFIED",
        "references": [
          "b7c4e882-7881-4bd5-ae4e-cafeecaad71f",
          "25e4d1d5-f985-45e8-8266-34a464156b0f"
        ],
        "stereo_centers": 3
      },
      "unii": "3H9QKO17ON"
    }
  ]
}