{ "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": "ecfd70dc-0a0a-47df-99c7-7724ad8caab7", "code": "45322-31-4", "type": "PRIMARY", "url": "https://commonchemistry.cas.org/detail?cas_rn=45322-31-4", "code_system": "CAS", "references": [ "8f65236f-719a-43fc-8e29-ddec3a9702e4", "4cfc2c2c-3e2d-4e6c-8ac1-2667ff4a36ef" ] }, { "uuid": "ab2ca800-2159-48db-8c7e-cdd6b672066d", "code": "256-234-0", "type": "PRIMARY", "url": "https://echa.europa.eu/substance-information/-/substanceinfo/100.051.105", "code_system": "ECHA (EC/EINECS)", "references": [ "8f65236f-719a-43fc-8e29-ddec3a9702e4" ] }, { "uuid": "4b48a22a-5816-445d-b937-02ade9562a32", "code": "6365474", "type": "PRIMARY", "url": "https://pubchem.ncbi.nlm.nih.gov/compound/6365474", "code_system": "PUBCHEM", "references": [ "8f65236f-719a-43fc-8e29-ddec3a9702e4" ] }, { "uuid": "6c4fe5cc-ee2d-8068-6843-5f076fc3fa2b", "code": "DTXSID001316165", "type": "PRIMARY", "url": "https://comptox.epa.gov/dashboard/chemical/details/DTXSID001316165", "code_system": "EPA CompTox", "references": [ "6a83b0ba-17dc-57e0-5433-123283e39681" ] }, { "uuid": "ff9ca46a-39aa-4e59-a8b2-c33615b21afe", "code": "1IZ2U11X1E", "type": "PRIMARY", "code_system": "FDA UNII" } ], "substance_class": "chemical", "names": [ { "uuid": "f2404115-b0eb-4afe-8008-2693f55376db", "name": "2-BUTENEDIOIC ACID (2E)-, 1,4-DIDOCOSYL ESTER", "stdName": "2-BUTENEDIOIC ACID (2E)-, 1,4-DIDOCOSYL ESTER", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "2926e7a7-7ce3-4582-9fe0-194e1ff53f79" ], "display_name": false }, { "uuid": "fded65e7-4b35-46c6-9505-a6a8ab4e6d65", "name": "2-BUTENEDIOIC ACID (2E)-, DIDOCOSYL ESTER", "stdName": "2-BUTENEDIOIC ACID (2E)-, DIDOCOSYL ESTER", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "2926e7a7-7ce3-4582-9fe0-194e1ff53f79" ], "display_name": false }, { "uuid": "7d32c1e8-9f30-480c-b28d-522e70984d33", "name": "2-BUTENEDIOIC ACID (E)-, DIDOCOSYL ESTER", "stdName": "2-BUTENEDIOIC ACID (E)-, DIDOCOSYL ESTER", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "2926e7a7-7ce3-4582-9fe0-194e1ff53f79" ], "display_name": false }, { "uuid": "ea872a82-0ddb-4447-a3e0-197c676a283e", "name": "DIBEHENYL FUMARATE", "stdName": "DIBEHENYL FUMARATE", "type": "of", "languages": [ "en" ], "preferred": false, "references": [ "e70aa012-3048-443d-aa20-4d4c97e4a18a", "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "2926e7a7-7ce3-4582-9fe0-194e1ff53f79", "aa88999a-4721-4715-a2c7-c0c7e3a1d3a4" ], "display_name": true, "domains": [ "cosmetic" ], "name_orgs": [ { "uuid": "1594867a-196e-4ba2-86f1-e4140d0f0e3e", "name_org": "INCI" } ] }, { "uuid": "eabcc169-3648-4923-a4a9-534ee02f8385", "name": "DIDOCOSYL FUMARATE", "stdName": "DIDOCOSYL FUMARATE", "type": "sys", "languages": [ "en" ], "preferred": false, "references": [ "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "2926e7a7-7ce3-4582-9fe0-194e1ff53f79" ], "display_name": false }, { "uuid": "70c321c7-d073-41f5-9d96-a6dc930f9f63", "name": "MARRIX 222", "stdName": "MARRIX 222", "type": "bn", "languages": [ "en" ], "preferred": false, "references": [ "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "2926e7a7-7ce3-4582-9fe0-194e1ff53f79" ], "display_name": false } ], "references": [ { "uuid": "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "citation": "STN", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN", "PUBLIC_DOMAIN_RELEASE", "AUTO_SELECTED" ] }, { "uuid": "2926e7a7-7ce3-4582-9fe0-194e1ff53f79", "citation": "STN (SCIFINDER)", "doc_type": "STN (SCIFINDER)", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "e70aa012-3048-443d-aa20-4d4c97e4a18a", "citation": "PCPC", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "8f65236f-719a-43fc-8e29-ddec3a9702e4", "citation": "SRS CODE IMPORT", "doc_type": "SRS", "public_domain": true, "document_date": 1493391493000, "tags": [ "NOMEN" ] }, { "uuid": "82dfa224-3778-4f5b-9eb9-903939c2e916", "citation": "SRS import [1IZ2U11X1E]", "url": "http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=1IZ2U11X1E", "doc_type": "SRS", "public_domain": true, "document_date": 1493391493000, "tags": [ "NOMEN" ] }, { "uuid": "aa88999a-4721-4715-a2c7-c0c7e3a1d3a4", "citation": "DIBEHENYL FUMARATE [INCI]", "doc_type": "SRS_LOCATOR", "public_domain": true }, { "uuid": "4cfc2c2c-3e2d-4e6c-8ac1-2667ff4a36ef", "citation": "STN", "doc_type": "STN (SCIFINDER)", "public_domain": true }, { "uuid": "6a83b0ba-17dc-57e0-5433-123283e39681", "citation": "EPA CompTox", "doc_type": "EPA", "public_domain": true } ], "definition_type": "PRIMARY", "moieties": [ { "uuid": "ffca08da-a6b7-4441-9fe6-34012e78cde3", "id": "ffca08da-a6b7-4441-9fe6-34012e78cde3", "molfile": "\n Marvin 01132113142D \n\n 52 51 0 0 0 0 999 V2000\n 11.4437 4.9626 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.4437 4.1376 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.1581 3.7251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.1581 2.9001 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.8726 2.4876 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.8726 1.6626 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5871 1.2501 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5871 0.4251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.3015 0.0126 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.3015 -0.8124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.0160 -1.2249 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.0160 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.3015 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5871 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.8726 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.1581 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.4437 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.7292 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.0147 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.3003 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.5858 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.8713 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.1568 -2.4624 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.1568 -3.2874 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.8713 -3.6999 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.4423 -3.6999 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.4423 -4.5249 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.7279 -4.9374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -4.5250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.7279 -5.7624 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -6.1750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -7.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2989 -7.4124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2989 -8.2374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -8.6500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -9.4750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -9.8874 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -10.7124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1555 -11.1250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1556 -11.9500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 1.4411 -12.3624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 1.4411 -13.1874 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1556 -13.6000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1556 -14.4250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -14.8374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -15.6624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -16.0750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -16.9000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2990 -17.3125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2990 -18.1375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -18.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -19.3750 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 10 9 1 0 0 0 0\n 11 10 1 0 0 0 0\n 12 11 1 0 0 0 0\n 13 12 1 0 0 0 0\n 14 13 1 0 0 0 0\n 15 14 1 0 0 0 0\n 16 15 1 0 0 0 0\n 17 16 1 0 0 0 0\n 18 17 1 0 0 0 0\n 19 18 1 0 0 0 0\n 20 19 1 0 0 0 0\n 21 20 1 0 0 0 0\n 22 21 1 0 0 0 0\n 23 22 1 0 0 0 0\n 24 23 1 0 0 0 0\n 24 25 2 0 0 0 0\n 26 24 1 0 0 0 0\n 27 26 2 0 0 0 0\n 27 28 1 0 0 0 0\n 28 29 2 0 0 0 0\n 28 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 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 42 43 1 0 0 0 0\n 43 44 1 0 0 0 0\n 44 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\nM END", "smiles": "CCCCCCCCCCCCCCCCCCCCCCOC(=O)/C=C/C(=O)OCCCCCCCCCCCCCCCCCCCCCC", "formula": "C48H92O4", "atropisomerism": "No", "charge": 0, "count": 1, "stereochemistry": "ACHIRAL", "count_amount": { "type": "MOL RATIO", "average": 1, "units": "MOL RATIO", "uuid": "c524ac19-d2fa-4304-9e8b-fbb1d2bcf41d" }, "defined_stereo": 0, "ez_centers": 1, "molecular_weight": "733.2435", "optical_activity": "NONE", "stereo_centers": 0 } ], "definition_level": "COMPLETE", "uuid": "ca85f07c-0bc2-4853-a917-d68230b7d478", "version": "4", "structure": { "id": "e56d87ba-154e-446b-8a91-a52f842df766", "molfile": "\n Marvin 01132111532D \n\n 52 51 0 0 0 0 999 V2000\n 6.4423 -3.6999 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.1568 -3.2874 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.1568 -2.4624 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.8713 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.5858 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.3003 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.0147 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.7292 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.4437 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.1581 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.8726 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5871 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.3015 -2.4624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.0160 -2.0499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.0160 -1.2249 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.3015 -0.8124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.3015 0.0126 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5871 0.4251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5871 1.2501 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.8726 1.6626 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.8726 2.4876 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.1581 2.9001 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.1581 3.7251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.4437 4.1376 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.4437 4.9626 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.8713 -3.6999 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -4.5250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -19.3750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -18.5500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2990 -18.1375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2990 -17.3125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -16.9000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -16.0750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -15.6624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -14.8374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1556 -14.4250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1556 -13.6000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 1.4411 -13.1874 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 1.4411 -12.3624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1556 -11.9500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.1555 -11.1250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -10.7124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 2.8700 -9.8874 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -9.4750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.5845 -8.6500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2989 -8.2374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2989 -7.4124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -7.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0134 -6.1750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.7279 -5.7624 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.7279 -4.9374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.4423 -4.5249 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 4 5 1 0 0 0 0\n 5 6 1 0 0 0 0\n 6 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 17 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 23 24 1 0 0 0 0\n 24 25 1 0 0 0 0\n 2 26 2 0 0 0 0\n 51 27 2 0 0 0 0\n 29 28 1 0 0 0 0\n 30 29 1 0 0 0 0\n 31 30 1 0 0 0 0\n 32 31 1 0 0 0 0\n 33 32 1 0 0 0 0\n 34 33 1 0 0 0 0\n 35 34 1 0 0 0 0\n 36 35 1 0 0 0 0\n 37 36 1 0 0 0 0\n 38 37 1 0 0 0 0\n 39 38 1 0 0 0 0\n 40 39 1 0 0 0 0\n 41 40 1 0 0 0 0\n 42 41 1 0 0 0 0\n 43 42 1 0 0 0 0\n 44 43 1 0 0 0 0\n 45 44 1 0 0 0 0\n 46 45 1 0 0 0 0\n 47 46 1 0 0 0 0\n 48 47 1 0 0 0 0\n 49 48 1 0 0 0 0\n 50 49 1 0 0 0 0\n 51 50 1 0 0 0 0\n 52 51 1 0 0 0 0\n 52 1 2 0 0 0 0\nM END", "smiles": "CCCCCCCCCCCCCCCCCCCCCCOC(=O)/C=C/C(=O)OCCCCCCCCCCCCCCCCCCCCCC", "formula": "C48H92O4", "atropisomerism": "No", "charge": 0, "count": 1, "stereochemistry": "ACHIRAL", "defined_stereo": 0, "ez_centers": 1, "molecular_weight": "733.2435", "optical_activity": "NONE", "references": [ "6e69638c-8d5a-4cd2-94a4-0b1809260d33", "82dfa224-3778-4f5b-9eb9-903939c2e916" ], "stereo_centers": 0 }, "unii": "1IZ2U11X1E" } ] }