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About This Item
Empirical Formula (Hill Notation):
C13H17NO2
CAS Number:
Molecular Weight:
219.28
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
243-020-7
MDL number:
Assay:
99% (CP)
InChI key
INGSNVSERUZOAK-UHFFFAOYSA-N
InChI
1S/C13H17NO2/c15-13(16)12(10-6-2-1-3-7-10)11-8-4-5-9-14-11/h1-3,6-7,11-12,14H,4-5,8-9H2,(H,15,16)
SMILES string
OC(=O)C(C1CCCCN1)c2ccccc2
assay
99% (CP)
Quality Level
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Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A Solans et al.
Journal of chromatography. B, Biomedical applications, 658(2), 380-384 (1994-08-19)
Two analytical methods for the simultaneous detection in urine of methylphenidate and its main metabolite, ritalinic acid, are described. Both procedures are based on solid-phase extraction of urine samples on Bond Elut Certify columns, and capillary gas chromatographic-mass spectrometric detection
Ragnar Thomsen et al.
Journal of analytical toxicology, 36(8), 560-568 (2012-07-27)
A chiral liquid chromatography tandem mass spectrometry (LC-MS-MS) method was developed and validated for quantifying methylphenidate and its major metabolite ritalinic acid in blood from forensic cases. Blood samples were prepared in a fully automated system by protein precipitation followed
C L DeVane et al.
Journal of clinical psychopharmacology, 20(3), 347-349 (2000-06-01)
Six adults phenotyped as either extensive (N = 4) or poor (N = 2) metabolizers for cytochrome P450 (CYP) 2D6 were given a 10-mg oral dose of methylphenidate (MPH) on two separate occasions with and without quinidine, a potent CYP2D6
J S Markowitz et al.
Journal of clinical psychopharmacology, 19(4), 362-366 (1999-08-10)
Methylphenidate is the most commonly prescribed psychostimulant in clinical use today. Known methylphenidate metabolites include ritalinic acid, corresponding lactams, and p-hydroxymethylphenidate. Recent in vitro work using rat liver preparations has indicated that the methylphenidate ethyl ester, ethylphenidate, is formed upon
Martin Josefsson et al.
Journal of pharmaceutical and biomedical analysis, 55(5), 1050-1059 (2011-04-19)
A validated, accurate and sensitive LC-MS/MS method for determination of racemic methylphenidate and its metabolite ritalinic acid has been developed. The analytes were quantified by tandem mass spectrometry operating in positive electrospray ionization mode with multiple reaction monitoring. Blood, plasma
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