{ "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": "60ed6580-5bd3-2574-ead0-3aeca62e63ed", "code": "138059634", "type": "PRIMARY", "url": "https://pubchem.ncbi.nlm.nih.gov/compound/138059634", "code_system": "PUBCHEM", "references": [ "3338d6bf-1db2-e1c6-1171-b3c0f943dede" ] }, { "uuid": "a112474e-a86d-4c72-afde-f7549d15f03a", "code": "N358T8719L", "type": "PRIMARY", "code_system": "FDA UNII" } ], "substance_class": "chemical", "names": [ { "uuid": "7a709210-5848-45ed-a2de-3e537f13fc4b", "name": "COLATERIC DLB", "stdName": "COLATERIC DLB", "type": "bn", "languages": [ "en" ], "preferred": false, "references": [ "00e43ca6-3a3f-4db9-89bf-ade5bc96cd8c", "eef15109-d03a-43c2-b71c-be5ed82e5845" ], "display_name": false }, { "uuid": "f1764d2c-7bd8-4767-9b61-3807e7c4285e", "name": "DIMER DILINOLEAMIDOPROPYL DIBETAINE", "stdName": "DIMER DILINOLEAMIDOPROPYL DIBETAINE", "type": "of", "languages": [ "en" ], "preferred": false, "references": [ "00e43ca6-3a3f-4db9-89bf-ade5bc96cd8c", "ac5213a5-c04a-4e65-b969-2f69d3f36a38", "eef15109-d03a-43c2-b71c-be5ed82e5845" ], "display_name": true, "domains": [ "cosmetic" ], "name_orgs": [ { "uuid": "4af6c209-ee3f-4003-a840-299d84ca7c69", "name_org": "INCI" } ] } ], "references": [ { "uuid": "eef15109-d03a-43c2-b71c-be5ed82e5845", "citation": "PCPC-DB", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN", "PUBLIC_DOMAIN_RELEASE", "AUTO_SELECTED" ] }, { "uuid": "00e43ca6-3a3f-4db9-89bf-ade5bc96cd8c", "citation": "PERSONAL CARE PRODUCTS COUNCIL", "doc_type": "PERSONAL CARE PRODUCTS COUNCIL", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "81a7dd6c-f622-4a53-9c56-c9927fe410c4", "citation": "SRS import [N358T8719L]", "url": "http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=N358T8719L", "doc_type": "SRS", "public_domain": true, "document_date": 1493392605000, "tags": [ "NOMEN" ] }, { "uuid": "e9a5ada4-c71c-4708-a315-35b7c0d8c36d", "citation": "http://colonialchem.com/admin/uploads/COLATERIC%20DLB.pdf", "url": "http://colonialchem.com/admin/uploads/COLATERIC%20DLB.pdf", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "ac5213a5-c04a-4e65-b969-2f69d3f36a38", "citation": "DIMER DILINOLEAMIDOPROPYL DIBETAINE [INCI]", "doc_type": "SRS_LOCATOR", "public_domain": true }, { "uuid": "3338d6bf-1db2-e1c6-1171-b3c0f943dede", "citation": "PUBCHEM", "doc_type": "PUBCHEM", "public_domain": true } ], "definition_type": "PRIMARY", "moieties": [ { "uuid": "b2d5d898-44bc-4efb-b704-791e0b71e6e2", "id": "b2d5d898-44bc-4efb-b704-791e0b71e6e2", "molfile": "\n Marvin 01132109162D \n\n 60 60 0 0 0 0 999 V2000\n 8.8499 -20.5131 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.4316 -19.9281 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.2155 -19.1318 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.7971 -18.5467 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.5813 -17.7505 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.1628 -17.1654 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.9468 -16.3691 0.0000 C 0 0 0 0 0 0 0 0 0 3 0 0\n 9.1488 -16.1601 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.9333 -15.3619 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.5144 -14.7789 0.0000 C 0 0 0 0 0 0 0 0 0 3 0 0\n 9.2989 -13.9805 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.8806 -13.3953 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.6646 -12.5992 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.8473 -12.0744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.8863 -11.2504 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.1920 -10.8048 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.2309 -9.9806 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5367 -9.5350 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.8036 -9.9133 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5757 -8.7109 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 6.8815 -8.2652 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.9203 -7.4411 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.2261 -6.9953 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.2650 -6.1712 0.0000 N 0 3 0 0 0 0 0 0 0 3 0 0\n 6.4465 -5.3663 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.0826 -6.2818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.4791 -5.9203 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.3034 -5.1142 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.5174 -4.8633 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0\n 5.9137 -4.5589 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 10.3123 -14.9880 0.0000 C 0 0 0 0 0 0 0 0 0 3 0 0\n 10.8935 -14.4049 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.6915 -14.6139 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.2726 -14.0308 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.0706 -14.2397 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.6521 -13.6546 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.4501 -13.8635 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.0311 -13.2804 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.8113 -13.8165 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 16.5559 -13.4612 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 17.2359 -13.9285 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 17.1712 -14.7510 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 17.9805 -13.5732 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 18.6604 -14.0405 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 19.4051 -13.6852 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 20.0850 -14.1525 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 20.8296 -13.7973 0.0000 N 0 3 0 0 0 0 0 0 0 3 0 0\n 21.5012 -13.3181 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 20.4108 -13.0864 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 21.3654 -14.4246 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 22.1767 -14.2741 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 22.4520 -13.4964 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0\n 22.7126 -14.9014 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 10.5284 -15.7840 0.0000 C 0 0 0 0 0 0 0 0 0 3 0 0\n 11.3265 -15.9930 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.5419 -16.7913 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.3398 -17.0002 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.5553 -17.7986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.3534 -18.0076 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5688 -18.8059 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 54 7 1 0 0 0 0\n 8 9 2 0 0 0 0\n 10 9 1 0 0 0 0\n 11 10 1 0 0 0 0\n 31 10 1 0 0 0 0\n 12 11 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 2 0 0 0 0\n 18 20 1 0 0 0 0\n 21 20 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 24 26 1 0 0 0 0\n 24 27 1 0 0 0 0\n 27 28 1 0 0 0 0\n 28 29 1 0 0 0 0\n 28 30 2 0 0 0 0\n 31 32 1 0 0 0 0\n 31 54 1 0 0 0 0\n 33 32 2 3 0 0 0\n 34 33 1 0 0 0 0\n 35 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 2 0 0 0 0\n 41 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 48 47 1 0 0 0 0\n 49 47 1 0 0 0 0\n 47 50 1 0 0 0 0\n 50 51 1 0 0 0 0\n 52 51 1 0 0 0 0\n 53 51 2 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\nM CHG 4 24 1 29 -1 47 1 52 -1\nM END", "smiles": "CCCCCCC1C=CC(CCCCCCCC(=O)NCCC[N+](C)(C)CC(=O)[O-])C(C=CCCCCCCCC(=O)NCCC[N+](C)(C)CC(=O)[O-])C1CCCCCC", "formula": "C50H92N4O6", "atropisomerism": "No", "charge": 0, "count": 1, "stereochemistry": "MIXED", "count_amount": { "type": "MOL RATIO", "average": 1, "units": "MOL RATIO", "uuid": "7a091095-acf3-4dc6-9c7f-fc9287f97f96" }, "defined_stereo": 0, "ez_centers": 0, "molecular_weight": "845.2906", "optical_activity": "UNSPECIFIED", "stereo_centers": 4 } ], "definition_level": "REPRESENTATIVE", "uuid": "e869c869-ea0f-4d1f-9b5c-45da6582fcb5", "version": "6", "structure": { "id": "16d4c72f-e9f5-495d-bda6-cd7faadb1a76", "molfile": "\n Marvin 01132101232D \n\n 60 60 0 0 0 0 999 V2000\n 22.1767 -14.2741 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 22.4520 -13.4964 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0\n 21.3654 -14.4246 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 20.8296 -13.7973 0.0000 N 0 3 0 0 0 0 0 0 0 0 0 0\n 21.5012 -13.3181 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 20.4108 -13.0864 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 20.0850 -14.1525 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 19.4051 -13.6852 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 18.6604 -14.0405 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 17.9805 -13.5732 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 17.2359 -13.9285 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 17.1712 -14.7510 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 16.5559 -13.4612 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.8113 -13.8165 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.0311 -13.2804 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.4501 -13.8635 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.6521 -13.6546 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.0706 -14.2397 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.2726 -14.0308 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.6915 -14.6139 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.8935 -14.4049 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.3123 -14.9880 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.5144 -14.7789 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.2989 -13.9805 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.8806 -13.3953 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.6646 -12.5992 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.8473 -12.0744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.8863 -11.2504 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.1920 -10.8048 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.2309 -9.9806 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5367 -9.5350 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.8036 -9.9133 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5757 -8.7109 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 6.8815 -8.2652 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.9203 -7.4411 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.2261 -6.9953 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.2650 -6.1712 0.0000 N 0 3 0 0 0 0 0 0 0 0 0 0\n 5.4791 -5.9203 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.3034 -5.1142 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.5174 -4.8633 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.9137 -4.5589 0.0000 O 0 5 0 0 0 0 0 0 0 0 0 0\n 6.4465 -5.3663 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.0826 -6.2818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.9333 -15.3619 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.1488 -16.1601 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.9468 -16.3691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.1628 -17.1654 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.5813 -17.7505 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.7971 -18.5467 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.2155 -19.1318 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.4316 -19.9281 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.8499 -20.5131 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.5284 -15.7840 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.3265 -15.9930 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.5419 -16.7913 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.3398 -17.0002 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.5553 -17.7986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.3534 -18.0076 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5688 -18.8059 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 22.7126 -14.9014 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 2 1 1 0 0 0 0\n 3 1 1 0 0 0 0\n 4 3 1 0 0 0 0\n 5 4 1 0 0 0 0\n 6 4 1 0 0 0 0\n 7 4 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 11 12 2 0 0 0 0\n 13 11 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 18 19 1 0 0 0 0\n 19 20 1 0 0 0 0\n 20 21 2 3 0 0 0\n 22 21 1 0 0 0 0\n 22 23 1 0 0 0 0\n 24 23 1 0 0 0 0\n 25 24 1 0 0 0 0\n 25 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 29 30 1 0 0 0 0\n 30 31 1 0 0 0 0\n 31 32 2 0 0 0 0\n 31 33 1 0 0 0 0\n 34 33 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 2 0 0 0 0\n 39 41 1 0 0 0 0\n 37 42 1 0 0 0 0\n 37 43 1 0 0 0 0\n 23 44 1 0 0 0 0\n 45 44 2 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 53 46 1 0 0 0 0\n 22 53 1 0 0 0 0\n 53 54 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 60 1 2 0 0 0 0\nM CHG 4 2 -1 4 1 37 1 41 -1\nM END", "smiles": "CCCCCCC1C=CC(CCCCCCCC(=O)NCCC[N+](C)(C)CC(=O)[O-])C(C=CCCCCCCCC(=O)NCCC[N+](C)(C)CC(=O)[O-])C1CCCCCC", "formula": "C50H92N4O6", "atropisomerism": "No", "charge": 0, "count": 1, "stereochemistry": "MIXED", "defined_stereo": 0, "ez_centers": 0, "molecular_weight": "845.2906", "optical_activity": "UNSPECIFIED", "references": [ "e9a5ada4-c71c-4708-a315-35b7c0d8c36d", "81a7dd6c-f622-4a53-9c56-c9927fe410c4" ], "stereo_centers": 4 }, "unii": "N358T8719L" } ] }