D-THREO-METHYLPHENIDATE HYDROCHLORIDE

D-THREO-METHYLPHENIDATE HYDROCHLORIDE Structure
CAS No.
19262-68-1
Chemical Name:
D-THREO-METHYLPHENIDATE HYDROCHLORIDE
Synonyms
D03721;Focalin;Focalin (tn);D-METHYLPHENIDATE;Dexmethylphenidate HCl;d-threo-Methylphenidate;d-threo-Form hydrochloride;DEXMETHYLPHENIDATE HYDROCHLORIDE;Methylphenidate-d6 hydrochloride;DexaMethylphenedate Hydrochloride
CBNumber:
CB8490337
Molecular Formula:
C14H20ClNO2
Molecular Weight:
269.77
MOL File:
19262-68-1.mol
Modify Date:
2023/5/15 10:44:00

D-THREO-METHYLPHENIDATE HYDROCHLORIDE Properties

Melting point 218-220°C
storage temp. Controlled Substance, -20°C Freezer
solubility Methanol (Slightly), Water (Slightly)
form Solid
color White to Off-White

SAFETY

Risk and Safety Statements

Hazard Codes  Xn
Risk Statements  22
RTECS  TM3850000

D-THREO-METHYLPHENIDATE HYDROCHLORIDE Chemical Properties,Uses,Production

Description

Dexmethylphenidate, the pharmacologically effective enantiomer of d,l-methyl phenidate (Ritalin?) was developed as an improved treatment for attention deficit hyperactivity disorder (ADHD) in children. Dexmethylphenidate acts via the inhibition of reuptake of dopamine (by binding to dopamine transporter) and nor-adrenaline. It is thought to block dopamine and noradrenaline reuptake into the presynaptic neuron and increase neurotmnsmitter release into the extraneuronal space. Dexmethytphenidate, at half the usual dose of racemic methylphenidate, improved the symptoms of attention deficit hyperactivity disorder to a similar extent to methylphenidate in both home and school settings (SNAP-ADHD scores) at 3 h post dosing. Moreover, some studies showed that dexmethylphenidate has a statistically significant longer duration of action than the racemic form as measured by a behavioral scale at 6 h post dosing compared to placebo. In patients with ADHD, plasma dexmethylphenidate concentrations increased rapidly, reaching a maximum in the fasted state at approximately l-l.5 h post-dose. The mean plasma half-life for dexmethylphenidate is approximately 2.2 h. Dexmethylphenidate is metabolized to d-α-phenyl-piperidine acetic acid, its main urinary metabolite which has negligible pharmacological activity. In vitro studies showed that dexmethylphenidate did not inhibit cytochrome P450 isozymes. Dexmethylphenidate was well tolerated; the most commonly reported adverse events (abdominal pain, headache, anorexia, insomnia) were mild in severity and consistent with those known to be associated with agents containing methylphenidate. Current labeling states that dexmethylphenidate should be administered twice daily with an interval of at least 4 hours between doses. Stimulant medications have been used for over sixty years and remain, until now, the first line pharmacological therapy for children with ADHD, demonstrating effectiveness in roughly 70% of patients.

Chemical Properties

White Solid

Uses

Controlled substance. CNS stimulant. More potent enantiomer

D-THREO-METHYLPHENIDATE HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

(2R)-2-Phenyl-2-[(R)-2-piperidinyl]acetic acid methyl ester (R)-[(2R)-Hexahydropyridine-2-yl]phenylacetic acid methyl ester (R)-2-Phenyl-2-[(R)-2-piperidinyl]acetic acid methyl ester [(αR,2R)-α-Phenyl-2β-piperidineacetic acid]methyl ester d-threo-Methylphenidate D03721 Dexmethylphenidate hydrochloride (usan) Focalin Focalin (tn) D-erythro-Methylphenidate Hydrochloride DexaMethylphenedate Hydrochloride d-threo-Form hydrochloride DEXMETHYLPHENIDATE HYDROCHLORIDE D-THREO-METHYLPHENIDATE HYDROCHLORIDE D-METHYLPHENIDATE (2R,2’R)-(+)-threo-Methyl a-Phenyl-a-(2-piperidyl)acetate Hydrochloride Dexmethylphenidate HCl (R)-methyl 2-phenyl-2-((R)-piperidin-2-yl)acetate hydrochloride D-threo-Methylphenidate Hydrochloride (1.0mg/ml in Methanol) Dexmethylphenidate HydrochlorideQ: What is Dexmethylphenidate Hydrochloride Q: What is the CAS Number of Dexmethylphenidate Hydrochloride Q: What is the storage condition of Dexmethylphenidate Hydrochloride methyl (R)-2-phenyl-2-((R)-piperidin-2-yl)acetate Methylphenidate-d6 hydrochloride 19262-68-1 Aromatics Chiral Reagents Intermediates & Fine Chemicals Pharmaceuticals