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perhexiline

Product Name
perhexiline
CAS No.
6621-47-2
Chemical Name
perhexiline
Synonyms
perhexilene;perhexiline;Perhexilline;Perhexiline USP/EP/BP;Perhexiline (Mixture of Diastereomers);(S)-2-(2,2-Dicyclohexylethyl)piperidine;(R)-2-(2,2-Dicyclohexylethyl)piperidine;(2S)-2-(2,2-Dicyclohexylethyl)piperidine;(2R)-2-(2,2-Dicyclohexylethyl)piperidine
CBNumber
CB0875583
Molecular Formula
C19H35N
Formula Weight
277.49
MOL File
6621-47-2.mol
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perhexiline Property

Boiling point:
340.0±10.0 °C(Predicted)
Density 
0.926±0.06 g/cm3(Predicted)
pka
pKa 10.36 ± 0.06(40% EtOH,t =25,) (Uncertain)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0013549
Product name
PERHEXILINE
Purity
95.00%
Packaging
5MG
Price
$504.88
Updated
2021/12/16
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perhexiline Chemical Properties,Usage,Production

Originator

Pexid, Merrell-Tourade ,France ,1973

Uses

Vasodilator (coronary).

Definition

ChEBI: Perhexiline is a member of piperidines. It has a role as a cardiovascular drug.

Manufacturing Process

1,1-Dicyclohexyl-2-(2'-pyridyl)ethanol hydrochloride (5 grams) was dehydrated by heating with 25 ml of concentrated hydrochloric acid at steam bath temperature for 10 minutes. 70 ml of water were added to the reaction mixture to give the crystalline hydrochloride salt. The product, 1,1dicyclohexyl-2-(2'-pyridyl)ethylene hydrochloride, was recrystallized from methanol-ethyl acetate to yield a white solid melting at 150°-151.5°C.
1,1-Dicyclohexyl-2-(2'-pyridyl)ethylene hydrochloride (15 grams) in 150 ml of ethanol was hydrogenated in the presence of platinum oxide at about 60 pounds per square inch of hydrogen pressure. The product, 1,1-dicyclohexyl2-(2'-piperidyl)ethane hydrochloride, crystallized from a mixture of methanol and methyl ethyl ketone as a white solid melting at 243° to 245.5°C.
The hydrochloride salt was neutralized with 10% sodium hydroxide solution and the free base so produced was dissolved in ether. The ether solution was dried over anhydrous magnesium sulfate. Addition of an excess of maleic acid in methanol to the solution yielded the acid maleate salt which melted at 188.5°-191°C.
The starting material was obtained by reacting ethyl formate with cyclohexylmagnesium bromide to give dicyclohexylcarbinol. That is oxidized to dicyclohexylketone and then reacted with α-picoline.

brand name

Pexid (Marion Merrell Dow).

Therapeutic Function

Coronary vasodilator

Enzyme inhibitor

This calcium-blocking vasodilator (FW = 277.49 g/mol; CAS 6621-47-2; typically supplied as the maleate or HCl salt), also known as Pexid? and 2- (2,2-dicyclohexylethyl)piperidine, is used to treat angina. It does so by targetting carnitine palmitoyltransferase-1 (CPT-1), an enzyme that controls the access of long chain fatty acids to the mitochondrial site of b-oxidation, showing concentration-dependent inhibition in vitro, using rat cardiac mitochondria, IC50 = 77 μM, and hepatic mitochondria, IC50 = 148 μM. Amiodarone, another drug with anti-anginal properties, likewise inhibits cardiac CPT-1 (IC50 = 228 μM). The rank order of potency for inhibition was malonyl-CoA > 4-hydroxyphenylglyoxylate = perhexiline > amiodarone = monohydroxy-perhexiline. Inhibition was competitive with respect to palmitoyl-CoA but non-competitive inhibition with respect to carnitine. This shifts myocardial metabolism from fatty acid to glucose utilisation which results in increased ATP production for the same O2 consumption and consequently increases myocardial efficiency. (See also Meldonium) Other Target(s): CYP2D6; glutathione S-transferase; Mg2+-ATPase; NADH dehydrogenase; Na+ /K+ -exchanging ATPase; b-oxidation; oxidative phosphorylation; and succinate dehydrogenase.

perhexiline Preparation Products And Raw materials

Raw materials

Preparation Products

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perhexiline Suppliers

BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
14059
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65
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9926
Advantage
65
Chongqing Chemieliva Pharmaceutical Co., Ltd.
Tel
023-67770219
Fax
+86 (23) 6777-0220
Email
jessica.hu@chemieliva.com
Country
China
ProdList
1426
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60
Wuhan Magic Biological Technology Co., Ltd.
Tel
18872289958、027-52304252、3400508168
Fax
027-52304252
Email
3400508168@qq.com
Country
China
ProdList
1910
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Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
28761
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-89586680 +86-18192503167
Fax
+86-29-88380327
Email
1026@dideu.com
Country
China
ProdList
9126
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58
CONIER CHEM AND PHARMA LIMITED
Tel
+8618523575427
Email
sales@conier.com
Country
China
ProdList
49391
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58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24024
Advantage
58
Shaanxi Dideu Newmaterial Co., Ltd.
Tel
029-63373950 15353716720
Email
1052@dideu.com
Country
China
ProdList
10011
Advantage
58
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View Lastest Price from perhexiline manufacturers

Dideu Industries Group Limited
Product
Perhexiline
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons min
Release date
2021-08-06

6621-47-2, perhexilineRelated Search:


  • perhexilene
  • (2R)-2-(2,2-Dicyclohexylethyl)piperidine
  • (R)-2-(2,2-Dicyclohexylethyl)piperidine
  • (2S)-2-(2,2-Dicyclohexylethyl)piperidine
  • perhexiline
  • (S)-2-(2,2-Dicyclohexylethyl)piperidine
  • Perhexilline
  • Perhexiline (Mixture of Diastereomers)
  • Perhexiline USP/EP/BP
  • 6621-47-2
  • C19H35N