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CYCLANDELATE

CAS No.
456-59-7
Chemical Name:
CYCLANDELATE
Synonyms
bs572;Cydel;Natil;andeL;BS 572;Capilan;Anaspat;Lejopan;Dilatan;Novodil
CBNumber:
CB8668024
Molecular Formula:
C17H24O3
Molecular Weight:
276.37
MDL Number:
MFCD00056623
MOL File:
456-59-7.mol
MSDS File:
SDS
Last updated:2024-11-19 20:33:22

CYCLANDELATE Properties

Melting point 55.0-56.5°
Boiling point bp14 192-194°
Density 1.0535 (rough estimate)
refractive index 1.5490 (estimate)
storage temp. Sealed in dry,Room Temperature
Water Solubility Insoluble in water
solubility Chloroform (Slightly), Methanol (Slightly, Sonicated)
form powder to crystal
pka 12.13±0.20(Predicted)
color White to Almost white
Merck 14,2704
FDA UNII 4139O1OAY2
ATC code C04AX01
EPA Substance Registry System Benzeneacetic acid, .alpha.-hydroxy-, 3,3,5-trimethylcyclohexyl ester (456-59-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P
RTECS  OO8200000
HS Code  2918191350
Toxicity LD50 oral in rat: 5gm/kg

CYCLANDELATE price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical M0821 3,3,5-Trimethylcyclohexyl Mandelate (mixture of isomers) >94.0%(GC) 456-59-7 25g $130 2024-03-01 Buy
TRC C987625 Cyclandelate(>85%) 456-59-7 5g $870 2021-12-16 Buy
American Custom Chemicals Corporation API0002007 CICLOSPASMOL 95.00% 456-59-7 500G $1550 2021-12-16 Buy
American Custom Chemicals Corporation API0002007 CICLOSPASMOL 95.00% 456-59-7 250G $1900 2021-12-16 Buy
AK Scientific C403 Cyclandelate,mixtureofisomers 456-59-7 100g $201 2021-12-16 Buy
Product number Packaging Price Buy
M0821 25g $130 Buy
C987625 5g $870 Buy
API0002007 500G $1550 Buy
API0002007 250G $1900 Buy
C403 100g $201 Buy

CYCLANDELATE Chemical Properties,Uses,Production

Description

Almond (Amygdalus communis L) is a kind of nut from Xinjiang, China. Traditional Chinese medicine believes that almond can promote blood circulation to dispel blood stasis, lubricate bowels to relieve constipation, and relieve cough and asthma. The indications include amenorrhea, fever, wind arthralgia, malaria, blood stasis and pain, injuries, and blood stasis with constipation.

Physical properties

Appearance: white or almost white amorphous powder, special smell, and bitter taste. Solubility: very soluble in ethanol or acetone and almost insoluble in water. Melting point: 50–62 °C.

Originator

Cyclospasmol,Ives,US,1958

History

The chemical synthesis of cyclandelate was first synthesized by Funcke et al. from Elan Corporation in Ireland using a-hydroxyphenylacetic acid and cis-3,3,5-cycloalkyl cyclohexanol. The raw material of mandelic acid was obtained by hydrolysis after benzaldehyde reacted to sodium cyanide. However, sodium cyanide is hypertoxic, and because of its unique structure of a-hydroxy acid, it is easy to decompose under the acid condition, which leads to more by-products and low yield. A series of improved methods have been developed, which can reduce the environmental pollution under the premise of ensuring the yield of Zn/HCOONH4/ C2H5OH system . The method was used to synthesize cyclandelate since then. However, this drug has not yet been approved by the Food and Drug Administration in the United States, Canada, and other countries because it easily causes white blood cell deficiency. It has been withdrawn from the market after drug approval in Japan, France, and other countries in the 1970s.

Uses

vasodilator

Definition

ChEBI: The ester obtained by formal condensation of mandelic acid and 3,3,5-tricyclohexanol. It is a direct-acting smooth muscle relaxant used to dilate blood vessels.

Indications

The indications of cyclandelate are arteriosclerosis obliterans, acrocyanosis, cerebral arteriosclerosis, cerebral insufficiency, cerebrovascular disease, brain trauma, and post-traumatic brain syndrome.

Manufacturing Process

50 g of dl-mandelic acid are heated for 6 hours at approximately 100°C with 50 g of 3,3,5-trimethylcyclohexanol (mixture of cis and trans isomers), while passing dry hydrochloric acid gas as a catalyst through the mixture. The reaction product is subsequently poured out into water. After neutralization with potassium bicarbonate the ester is extracted with ether. The ether extract is dried with sodium sulfate, the ether is distilled off and the residue is distilled in vacuo. The fraction, which has a boiling point of 192° to 194°C at 14 mm, consists of the 3,3,5-trimethylcyclohexyl ester of mandelic acid, which is obtained in a yield of about 70%. The liquid solidifies to a colorless solid substance having a melting point of 50° to 53°C, according to US Patent 2,707,193. It has been found that crude cyclandelate may be purified by the following procedure. Crude cyclandelate is dissolved in a solvent chosen for convenience from the class of saturated hydrocarbons. The crude cyclandelate solution is stirred for a suitable interval, typically 1 to 5 hours, with an aqueous solution of sodium borohydride (NaBH4) at temperatures ranging from 25° to 65°C. The preferred temperature range is 40° to 50°C. The pH of the solution may be adjusted to any desired level in the range between 2.5 to 11.5. The preferred pH range is 8.0 to 11.0 because at lower pH levels borohydride is unstable and decomposes rapidly. The amount of sodium borohydride used ranges from about 0.5 to 2.0 wt % of the amount of cyclandelate present. At the end of the stirring period cyclandelate is recovered by well-known procedures. For instance, the aqueous organic layers may be separated gravimetrically and the product organic layer washed with an appropriate solvent and then distilled, according to US Patent 3,663,597.

brand name

Cyclospasmol (Wyeth-Ayerst).

Therapeutic Function

Spasmolytic

World Health Organization (WHO)

Cyclandelate is a papaverine type spasmolytic and vasodilating drug intended for symptomatic treatment of various peripheral vascular disorders, such as intermittent claudication in arteriosclerosis obliterans as well as a treatment for cognitive dysfunction in patients suffering from senile dementia of the multi-infarct or Alzheimer's type. Cyclandelate remains registered in several countries.

Pharmacology

The chemical structure and effect of cyclandelate are similar to papaverine. It can directly relax vascular smooth muscle and relieve the spasm of ileum and uterus smooth muscle induced by acetylcholine, histamine, and barium chloride in guinea pig. This effect is three to five times stronger than papaverine. Cyclandelate can also expand the cardiovascular, cerebrovascular, and renal blood vessels and limb peripheral vascular and coronary artery, increase blood flow, and promote blood circulation . It can also increase the tolerance to hypoxia, but the effect on human cerebral blood flow has not been confirmed. It was reported that cyclandelate can promote collateral circulation but has little effect on respiration, blood pressure, cardiac output, and myocardial oxygen consumption. It is safe for long-term administration .

Clinical Use

Cyclandelate can be used for clinical treatment of cerebral arteriosclerosis, cerebral vascular accident and its sequelae, post-traumatic brain syndrome, coronary arteriosclerosis, hypertensive heart disease, Raynaud’s disease, thromboangiitis obliterans, acrocyanosis, and Meniere’s disease .

116-02-9
611-73-4
456-59-7
Synthesis of CYCLANDELATE from 3,3,5-Trimethylcyclohexanol and Benzoylformic acid

CYCLANDELATE Preparation Products And Raw materials

Global( 171)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578 sales@hbmojin.com China 12839 58
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29881 58
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8810 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23541 58
AFINE CHEMICALS LIMITED
+86-0571-85134551 sales@afinechem.com China 15352 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com China 52849 58

View Lastest Price from CYCLANDELATE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cyclandelate pictures 2024-11-19 Cyclandelate
456-59-7
US $42.00 / mg 99.21% 10g TargetMol Chemicals Inc.
Cyclandelate pictures 2024-11-19 Cyclandelate
456-59-7
US $42.00 / mg 99.21% 10g TargetMol Chemicals Inc.
CYCLANDELATE pictures 2023-08-22 CYCLANDELATE
456-59-7
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
  • Cyclandelate pictures
  • Cyclandelate
    456-59-7
  • US $42.00 / mg
  • 99.21%
  • TargetMol Chemicals Inc.
  • Cyclandelate pictures
  • Cyclandelate
    456-59-7
  • US $42.00 / mg
  • 99.21%
  • TargetMol Chemicals Inc.
  • CYCLANDELATE pictures
  • CYCLANDELATE
    456-59-7
  • US $0.00 / KG
  • 99%
  • Hebei Mojin Biotechnology Co., Ltd
CYCLANDELATE 3,5,5-trimethylcyclohexylamygdalate 3,5,5-trimethylcyclohexylmandelate alpha-Hydroxybenzeneacetic acid 3,3,5-trimethylcyclohexyl ester alpha-hydroxybenzeneaceticacid3,3,5-trimethylcyclohexylester Arto-espasmol Benzeneacetic acid, alpha-hydroxy-, 3,3,5-trimethylcyclohexyl ester benzeneaceticacid,alpha-hydroxy-,3,3,5-trimethylcyclohexylester BS 572 bs572 Capilan 3,3,5-Trimethylcyclohexanol alpha-phenyl-alpha-hydroxyacetate 3,3,5-trimethylcyclohexanolalpha-phenyl-alpha-hydroxyacetate Ciclospasmol Clandilon MANDELIC ACID 3,3,5-TRIMETHYLCYCLOHEXYL ESTER 3,3,5-TRIMETHYLCYCLOHEXYL MANDELATE MANDELIC ACID 3,3,5-TRIMETHYLCYCLOHEXYL ESTER 98+% 3,3,5-Trimethylcyclohexanol α-phenyl-α-hydroxyacetate Benzeneacetic acid, α-hydroxy-, 3,3,5-trimethylcyclohexyl ester Cyclohexanol, 3,3,5-trimethyl-, mandelate (8CI) Mandelic acid, 3,3,5-trimethylcyclohexyl ester (6CI, 7CI, 8CI) Anaspat Ancyclin Cydel Lejopan (3,3,5-trimethylcyclohexyl) 2-hydroxy-2-phenylacetate (3,3,5-trimethylcyclohexyl) 2-hydroxy-2-phenyl-ethanoate 2-hydroxy-2-phenyl-acetic acid (3,3,5-trimethylcyclohexyl) ester Cyclandelate (200 mg) Cyclandelate, USP Cyclandelate Mandelic Acid 3,3,5-Trimethylcyclohexyl Ester 3,3,5-TriMethylcyclohexyl Mandelate (Mixture of isoMers) 3,3,5-Trimethylcyclohexyl hydroxy(phenyl)acetate 3,5,5-trimethylcyclohexanol,mandelicacidester 3,5,5-Trimethylcyclohexyl amygdalate Cyclandelate (mixture of isomers) Cyclergine Cyclobral Cyclolyt Cyclomandol Cyclospasmol Dilatan Natil Novodil Perebral Saiclate Sancyclan Sepyron Spasmione Spasmocyclon Spasmocyclone 5-Trimethylcyclohexyl mandelate 3,3,5-TrimethylcyclohexylMandelate(mixtureofisomers)> Trimethylcyclohexyl isomers andeL ate (mixture of isomers) CYCLANDELATE USP/EP/BP