Dolex Company Profile

Aggregated data from the web about Dolex

Company Name	Dolex
Website	https://www.dolex.com
Snippet	The verification code entered did not match the code sent to your phone.
KEGG	D00217 Y, C06804
UNII	362O9ITL9D
ChEBI	CHEBI:46195 Y
ChEMBL	ChEMBL112 Y
Country	united states
Density	1.263 g/cm3
Formula	C8H9NO2
Website	dolex.fr
ATC code	N02BE01 (WHO) N02BE51 (WHO) N02BE71 (WHO)
DrugBank	DB00316 Y
Industry	consumer electronics
linkedin	linkedin.com/company/dolex-inc
Excretion	Urine (85–90%)[3]
CAS Number	103-90-2 Y
ChemSpider	1906 Y
Drug class	Analgesics and antipyretics
IUPHAR/BPS	5239
Metabolism	Predominantly in the liver[3]
Molar mass	151.163 g·mol−1
PDB ligand	TYL (PDBe, RCSB PDB)
size_range	1 - 10
MedlinePlus	a681004
Metabolites	APAP gluc, APAP sulfate, APAP GSH, APAP cys, NAPQI[6]
Other names	N-acetyl-para-aminophenol (APAP), acetaminophen (USAN US)
PubChem CID	1983
PubChem SID	46506142
Trade names	Tylenol, Panadol, others[2]
display_url	dolex.fr
Headquarters	chamblee, georgia, united states
Legal status	AU: S4 (Rx), OTC, and unscheduled, UK: General sales list (GSL, OTC), US: OTC / Rx-only
License data	US DailyMed: Acetaminophen, US FDA: Acetaminophen
Boiling point	420 °C (788 °F)
ECHA InfoCard	100.002.870
Melting point	169 °C (336 °F) [10][11]
Pronunciation	Paracetamol: /ˌpærəˈsiːtəmɒl/Acetaminophen: /əˌsiːtəˈmɪnəfɪn/ (listen)
AHFS/Drugs.com	Monograph
Bioavailability	63–89%[4]:73
Onset of action	Pain relief onset by route:By mouth – 37 minutes[7]Buccal – 15 minutes[7]Intravenous – 8 minutes[7]
Protein binding	10–25%[5]
3D model (JSmol)	Interactive image
Pregnancycategory	AU: A [1], US: N (Not classified yet) [1],
Solubility in water	7.21 g/kg (0 °C)[9], 8.21 g/kg (5 °C)[9], 9.44 g/kg (10 °C)[9], 10.97 g/kg (15 °C)[9], 12.78 g/kg (20 °C)[9], ~14 mg/ml (20 °C)
Elimination half-life	2–2.5 hours[8]
CompTox Dashboard (EPA)	DTXSID2020006
Routes ofadministration	By mouth, through the cheek, rectal, intravenous (IV)

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