ABT-438 Hydroxy (CHEM122141)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-06 09:51:03 UTC | ||||||||
| Update Date | 2026-08-28 18:15:31 UTC | ||||||||
| Accession Number | CHEM122141 | ||||||||
| Identification | |||||||||
| Common Name | ABT-438 Hydroxy | ||||||||
| Class | Small Molecule | ||||||||
| Description | ABT-438 Hydroxy is an organic compound with the formula C16H16N2O2S and an average molecular weight of 300.40 g/mol. ABT-438 Hydroxy belongs to the 2,5-disubstituted thiophenes, a subclass of thiophenes within the organic compounds. It is further classified under the superclass of organoheterocyclic compounds. The compound has been identified in or released from 13 recorded sources across several diverse sectors. Within the electrical and electronic equipment sector, it is associated with capacitors, cell phones, batteries, printed circuit boards, wires and cables, and one additional source. It is found in healthcare, pharmaceuticals and veterinary products via medical devices, and in food, food processing and cookware through food packaging. In the energy, oil and gas sector as well as industrial manufacturing and chemical processing, it is present in lubricants. Additionally, it is found in textiles, leather and furnishings, specifically in synthetic textiles and carpets and rugs, along with one other sector. Recorded routes of exposure for ABT-438 Hydroxy include oral, inhalation, and touch. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type |
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| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C16H16N2O2S | ||||||||
| Average Molecular Mass | Not Available | ||||||||
| Monoisotopic Mass | 300.093 g/mol | ||||||||
| CAS Registry Number | Not Available | ||||||||
| IUPAC Name | 4-[5-[hydroxy(phenyl)methyl]thiophen-2-yl]but-3-yn-2-ylurea | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | CC(C#CC1=CC=C(S1)C(C2=CC=CC=C2)O)NC(=O)N | ||||||||
| InChI Identifier | InChI=1S/C16H16N2O2S/c1-11(18-16(17)20)7-8-13-9-10-14(21-13)15(19)12-5-3-2-4-6-12/h2-6,9-11,15,19H,1H3,(H3,17,18,20) | ||||||||
| InChI Key | HXOAUZPJYPAHKC-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
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| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
