ChemicalBook > CAS DataBase List > Methylphenidate hydrochloride

Methylphenidate hydrochloride

Product Name
Methylphenidate hydrochloride
CAS No.
298-59-9
Chemical Name
Methylphenidate hydrochloride
Synonyms
METHYLPHENIDATE HCL;Concerta;methylphenidate hydrochloride methanol*solution;Equasym;Metadate;Centedin;Centedrin;Centedrine;NSC 169868;Ciba 4311b
CBNumber
CB0188559
Molecular Formula
C14H20ClNO2
Formula Weight
269.77
MOL File
298-59-9.mol
More
Less

Methylphenidate hydrochloride Property

Melting point:
196-198?C
Flash point:
9℃
storage temp. 
Store at RT
solubility 
Freely soluble in water, soluble in ethanol (96 per cent), slightly soluble in methylene chloride.
form 
Powder
pka
8.9(at 25℃)
Water Solubility 
Soluble to 50 mM in water and to 100 mM in ethanol
BCS Class
2
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents, alkalies, barbiturates.
InChI
InChI=1S/C14H19NO2.ClH/c1-17-14(16)13(11-7-3-2-4-8-11)12-9-5-6-10-15-12;/h2-4,7-8,12-13,15H,5-6,9-10H2,1H3;1H
InChIKey
JUMYIBMBTDDLNG-UHFFFAOYSA-N
SMILES
C(C(=O)OC)(C1NCCCC1)C1C=CC=CC=1.Cl
CAS DataBase Reference
298-59-9(CAS DataBase Reference)
EPA Substance Registry System
Methylphenidate hydrochloride (298-59-9)
More
Less

Safety

Hazard Codes 
Xn,T,F
Risk Statements 
22-42-39/23/24/25-23/24/25-11
Safety Statements 
22-26-36-45-36/37-16
RIDADR 
3249
WGK Germany 
3
RTECS 
TM3850000
HazardClass 
6.1(b)
PackingGroup 
III
Toxicity
LD50 orally in mice: 190 mg/kg (Greenblatt, Osterberg)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P284Wear respiratory protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
M2892
Product name
Methylphenidate hydrochloride
Packaging
100mg
Price
$246
Updated
2024/03/01
Sigma-Aldrich
Product number
M-083
Product name
Methylphenidate hydrochloride solution
Purity
(Racemic mixture), ampule of 1?mL, 1.0?mg/mL in methanol (as free base), certified reference material, Cerilliant?
Packaging
1mL
Price
$27.7
Updated
2024/03/01
Sigma-Aldrich
Product number
M2892
Product name
Methylphenidate hydrochloride
Packaging
500mg
Price
$725
Updated
2024/03/01
Tocris
Product number
1812
Product name
Threo-methylphenidatehydrochloride
Purity
≥99%(HPLC)
Packaging
50
Price
$112
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003340
Product name
METHYLPHENIDATE HYDROCHLORIDE
Purity
95.00%
Packaging
25MG
Price
$750.75
Updated
2021/12/16
More
Less

Methylphenidate hydrochloride Chemical Properties,Usage,Production

Chemical Properties

white crystalline powder

Originator

Ritalin,Ciba,US,1958

Uses

Controlled substance (stimulant). CNS stimulant. Four isomers of Methylphenidate are known to exist. One pair of threo isomers and one pair of erythro are distinguished, from which only d-threo-Methyl phenidate exhibits the pharmacologically usually desired effects.

Uses

antiinflammatory

Uses

Methylphenidate (a.k.a., Ritalin) is a schedule II drug in the United States commonly used as a psychostimulant for the treatment of attention-deficit hyperactivity disorder. It blocks dopamine and norepinephrine transporters as well as facilitates NMDA-receptor mediated synaptic transmission through σ1 receptors via PLC/PKC signaling. This interaction with the σ1 receptor has been suggested to underlie methylphenidate’s considerable abuse potential and potential psychiatric side effects. This product is intended for forensic and biological research applications.[Cayman Chemical]

Manufacturing Process

As described in US Patent 2,507,631, 80 g of pulverized sodium amide are gradually added, while stirring and cooling, to a solution of 117 g of phenylacetonitrile and 113 g of 2-chloropyridine in 400 cc of absolute toluene. The mixture is then slowly heated to 110° to 120°C and maintained at this temperature for 1 hour. Water is added thereto after cooling, the toluene solution is shaken with dilute hydrochloric acid and the hydrochloric acid extracts are made alkaline with concentrated caustic soda solution. A solid mass is separated thereby which is taken up in acetic ester and distilled, αphenyl-α-pyridyl-(2)-acetonitrile passing over at 150° to 155°C under 0.5 mm pressure. When recrystallized from ethyl acetate it melts at 88° to 89°C, the yield amounting to 135 g.
100 g of α-phenyl-α-pyridyl-(2)-acetonitrile are introduced into 400 cc of concentrated sulfuric acid, allowed to stand overnight at room temperature, poured into ice and rendered alkaline with sodium carbonate. α-Phenyl-αpyridyl-(2)-acetamide is precipitated thereby which melts at 134°C after recrystallization from ethyl acetate.
100g of the resulting α-phenyl-α-pyridyl-(2)-acetamide, when dissolved in one liter of methyl alcohol and treated for 6 hours at water-bath temperature with hydrogen chloride, and after concentrating, diluting with water and rendering alkaline with sodium carbonate, yield 90 g of the α-phenyl-α-pyridyl-(2)-acetic acid methylester of MP 74° to 75°C (from alcohol of 50% strength).
The α-phenyl-α-piperidyl-(2)-acetic acid methylester of BP 135° to 137°C under 0.6 mm pressure is obtained in theoretical yield by hydrogenation of 50 g of α-phenyl-α-pyridyl(2)-acetic acid methylester in glacial acetic acid in the presence of 1 g of platinum catalyst at room temperature, while taking up 6 hydrogen atoms. Reaction with HCl gives the hydrochloride. Resolution of stereoisomers is described in US Patent 2,957,880.

Therapeutic Function

Psychostimulant

General Description

Because methylphenidate (Ritalin) has two asymmetriccenters, there are four possible isomers. The threo racemateis the marketed compound and is about 400 times aspotent as the erythro racemate.The absolute configurationof each of the threo-methylphenidate isomers has beendetermined.Considering that the structure is fairly complex(relative to amphetamine), it is likely that one of thetwo components of the threo racemate contains most of theactivity. Evidence indicates that the (+) -(2R,2'R)threoisomer is involved principally in the behavioral andpressor effects of the racemate.As is likely with many central psychomotor stimulants, there are multiple modesof action.
Methylphenidate, probably largely via its p-hydroxymetabolite, blocks NE reuptake, acts as a postsynapticagonist, depletes the same NE pools as reserpine, and haseffects on dopaminergic systems, such as blocking DAreuptake.
Methylphenidate is a potent CNS stimulant. Indicationsinclude narcolepsy and attention-deficit disorder.

General Description

Odorless white crystalline powder. Metallic taste. Solutions are acid to litmus. Absence of general acid/base catalysis.

Air & Water Reactions

Water soluble.

Reactivity Profile

Methylphenidate hydrochloride is incompatible with alkalis and solutions of barbiturates . Undergoes typical ester hydrolysis in aqueous solutions at 176°F.

Fire Hazard

Flash point data for Methylphenidate hydrochloride are not available; however, Methylphenidate hydrochloride is probably combustible.

Biological Activity

Psychomotor stimulant. Inhibitor of dopamine and noradrenalin transporters that increases the extracellular concentration of dopamine and noradrenalin. Increases locomotor activity in vivo .

Veterinary Drugs and Treatments

Methylphenidate may be useful for treating cataplexy/narcolepsy or hyperactivity in dogs.

storage

Store at RT

Methylphenidate hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Methylphenidate hydrochloride Suppliers

Hefei Lifeon Pharmaceutical Co.Ltd.
Tel
0551-65328450 18956095011
Fax
0551-65324089
Email
sales@lifeon.cn
Country
China
ProdList
23
Advantage
58
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15848
Advantage
69
Clearsynth Labs Limited
Tel
+91-22-26355700
Fax
+91-22-26355701
Email
info@clearsynth.com
Country
India
ProdList
9685
Advantage
58
Shanghai TaoSu Biochemical Technology Co., Ltd.
Tel
021-33632979
Fax
021-34692979
Email
info@tsbiochem.com
Country
China
ProdList
8073
Advantage
58
Shanghai Meishui Chemical Technology Co., Ltd
Tel
021-60549325 18616193163
Fax
021-33250306
Country
China
ProdList
4528
Advantage
56
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
D&C Chemicals
Tel
+86-21-58447131
Fax
+86-21-61642470
Email
1724405207@qq.com
Country
China
ProdList
472
Advantage
55
EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8449
Advantage
60
Shanghai Rechem science Co., Ltd.
Tel
21-31433387 15618786686
Fax
QQ:1369748377
Email
sales@rechemscience.com
Country
China
ProdList
2987
Advantage
58
Shanghai Chaolan Chemical Technology Center
Tel
QQ:65489617 15618227136
Fax
21-5161 9052
Email
info@SuperLan-chem.com
Country
China
ProdList
9365
Advantage
58
More
Less

View Lastest Price from Methylphenidate hydrochloride manufacturers

Wuhan Xinhao Biotechnology Co., Ltd
Product
methylphenidate hydrochloride methanol*solution 298-59-9
Price
US $10.00-100.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000 Metric Ton/Month
Release date
2024-01-17
Anhui Zhongda Biotechnology Co., Ltd
Product
Methylphenidate hydrochloride 298-59-9
Price
US $0.00-0.00/g
Min. Order
1g
Purity
99%
Supply Ability
100000tons
Release date
2023-08-09
Anhui Yiao New Material Technology Co., Ltd
Product
methylphenidate hydrochloride methanol*solution 298-59-9
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1 ton
Release date
2023-11-02

298-59-9, Methylphenidate hydrochlorideRelated Search:


  • METHYLPHENIDATE HCL
  • METHYLPHENIDATE HYDROCHLORIDE
  • RITALIN HYDROCHLORIDE
  • 2-piperidineaceticacid,alpha-phenyl-,methylester,hydrochloride
  • meridilhydrochloride
  • 2-Piperidineaceticacid, a-phenyl-, Methyl ester,hydrochloride (1:1)
  • Methylphenidate hydrochloride solution
  • Ritalin (Methylphenidate Hcl)
  • METHYL 2-PHENYL-2-(PIPERIDIN-2-YL)ACETATE HCL
  • JUMYIBMBTDDLNG-UHFFFAOYSA-N
  • Methylphenidate(Ritalin)
  • methylalpha-phenyl-2-piperidineacetatehydrochloride
  • methylphenidate hydrochloride methanol*solution
  • METHYLPHENIDATE HYDROCHLORIDE--DEA*SCHED
  • METHYLPHENIDATE HYDROCHLORIDE(RITALIN HYDROCHLORIDE)
  • Concerta
  • threo-methyl α-phenyl-α-(2-piperidyl)acetate hydrochloride
  • METHYLPHENIDATEHYDROCHLORIDE,USP
  • 2-Piperidineacetic acid, a-phenyl-, methyl ester, hydrochloride (6CI, 8CI, 9CI)
  • Centedrin
  • Centedrine
  • Metadate CD
  • Methyl a-phenyl-2-piperidineacetate hydrochloride
  • NSC 169868
  • Ritalin hydrochloride, threo-Methyl α-phenyl-α-(2-piperidyl)acetate hydrochloride
  • a-Phenyl-2-piperidineacetic Acid Methyl Ester Hydrochloride
  • Ciba 4311b
  • Equasym
  • Metadate
  • Methyl Phenidylacetate Hydrochloride
  • Methylphenidan Hydrochloride
  • Methyl phenyl(piperidin-2-yl)acetate hydrochloride
  • Centedin
  • Methylphenidate hydrochloride (ritalin)
  • Metilfenidat hydrochloride
  • Methylphenidate Hydrochloride (4:1 mixture of DL-erythro and DL-threo)
  • Threo-methylphenidate hydrochloride
  • Threo-methylα-Phenyl-2-piperidineacetatehydrochloride
  • Methylphenidate HCl, 1.0 mg/mL as free base
  • Methylphenidate HCl (Racemic mixture)
  • Methylphenidate Hydrochloride (CII), USP
  • Methylphenidate Hydrochloride CII (125 mg)
  • Methylphenidate-d9 HCl
  • Ritalin Impurity 10
  • Methyl (2RS)-phenyl[(2RS)-piperidin-2-yl]acetate hydrochloride
  • Methylphenidate hydrochloride USP/EP/BP
  • Methylphenidate HydrochlorideQ: What is Methylphenidate Hydrochloride Q: What is the CAS Number of Methylphenidate Hydrochloride Q: What is the storage condition of Methylphenidate Hydrochloride Q: What are the applications of Methylphenidate Hydrochloride
  • Methyl (2RS)-phenyl[(2SR)-piperidin-2-yl]acetate Hydrochloride
  • Amylmetacresol Impurity 12
  • 298-59-9
  • C14H19NO2HCl
  • C14H19NO2ClH
  • Heterocyclic Compounds
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • ASACOL
  • 298-59-9