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Xanthinol nicotinate

CAS No.
437-74-1
Chemical Name:
Xanthinol nicotinate
Synonyms
xavin;vedrin;sk331a;sadamin;contamex;teonicol;angiomin;stenalgil;complamin;complamex
CBNumber:
CB2255507
Molecular Formula:
C19H26N6O6
Molecular Weight:
434.45
MDL Number:
MFCD00058342
MOL File:
437-74-1.mol
Last updated:2024-04-23 16:18:34

Xanthinol nicotinate Properties

Melting point 180°
storage temp. Inert atmosphere,Room Temperature
solubility Water (Slightly)
form Solid
color White to Off-White
Water Solubility Water: 250 mg/mL (575.44 mM)
CAS DataBase Reference 437-74-1(CAS DataBase Reference)
FDA UNII 8G60H12X2D
ATC code C04AD02

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317-H319
Precautionary statements  P280-P305+P351+P338
WGK Germany  2
RTECS  QT1500000
HazardClass  IRRITANT

Xanthinol nicotinate price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC X499960 XanthinolNicotinate 437-74-1 10mg $85 2021-12-16 Buy
American Custom Chemicals Corporation API0004619 XANTHINOL NICOTINATE 95.00% 437-74-1 5G $123.9 2021-12-16 Buy
Matrix Scientific 059744 7-(2-Hydroxy-3-((2-hydroxyethyl)(methyl)amino)propyl)-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione nicotinate 437-74-1 500mg $199 2021-12-16 Buy
AK Scientific J54310 Xanthinolniacinate 437-74-1 1g $395 2021-12-16 Buy
AHH MT-60443 Xantinolnicotinate 98% 437-74-1 500g $450 2021-12-16 Buy
Product number Packaging Price Buy
X499960 10mg $85 Buy
API0004619 5G $123.9 Buy
059744 500mg $199 Buy
J54310 1g $395 Buy
MT-60443 500g $450 Buy

Xanthinol nicotinate Chemical Properties,Uses,Production

Uses

Sedative, Hypnotic

Uses

Xanthinol Nicotinate is a therapeutic agent that acts as a vasodilator.

Manufacturing Process

To a well-stirred solution of 740 parts by weight of epichlorohydrin in 200 parts by volume of isopropyl alcohol are added 600 parts by weight of methylaminoethanol during about 3 hours at 15°C to 20°C. The heat generated by the condensation is removed by means of a cooling bath. After the addition of the total quantity of methylaminoethanol, stirring is continued for 1 hour at 25°C. The condensation reaction is completed when development of heat reaction can no longer be observed. The solution thus produced of the raw 1-chloro-3-(methylhydroxyethylamino)-propanol-2 in isopropyl alcohol is a colorless viscous liquid which is used without further purification for the subsequent condensation with theophylline.
320 parts by weight of caustic soda are dissolved in 200 parts by weight of water and diluted with 6,000 parts by weight of isopropyl alcohol. 1,584 parts by weight of theophylline-hydrate are added to the well-stirred alcoholic caustic soda solution having a temperature between 50°C to 60°C. As a result, most of the theophylline sodium salt is precipitated and a doughy or pasty white reaction product is formed. While being stirred and heated to the boiling point of alcohol, the solution of the afore-described 1-chloro-3- (methylhydroxyethylamino)-propanol-2 is added dropwise into the reaction vessel during about 3 hours. After further cooking for 2 hours, the alcoholic solution of deposited sodium chloride is filtered off. By vaporizing the alcohol, the 3-(methylhydroxyethylamino)-2-hydroxypropyltheophylline can be obtained as a very viscous oil which contains impurities in the form of by- products.
For purpose of purification, the hot alcoholic solution is mixed with 975 parts by weight of nicotinic acid while being stirred and heated until the nicotinic acid is completely dissolved.
The 3-(methylhydroxyethylamino)-2-hydroxypropyltheophylline-nicotinate separates, while still being warm, in the form of shiny, thin, small sheets. After cooling, the crystallization product is sucked off from the mother liquor and recrystallized from 85% isopropyl alcohol.
The melting point of the pure nicotinic acid salt is 180°C and the yield is 75% to 80% related to the used theophylline. The substance has a nearly neutral reaction and is very readily soluble in water.

Therapeutic Function

Vasodilator

Xanthinol nicotinate Preparation Products And Raw materials

Global( 214)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12456 58
Ouhuang Engineering Materials (Hubei) Co., Ltd
+8617702722807 admin@hbouhuang.com China 1696 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282 alice@crovellbio.com China 8823 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5909 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387 1057@dideu.com China 3586 58

View Lastest Price from Xanthinol nicotinate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Xanthinol Nicotinate pictures 2024-04-23 Xanthinol Nicotinate
437-74-1
US $15.00 / kg 1kg 99.912% 10ton Ouhuang Engineering Materials (Hubei) Co., Ltd
Xanthinol nicotinate pictures 2023-07-01 Xanthinol nicotinate
437-74-1
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
Xanthinol nicotinate pictures 2021-09-29 Xanthinol nicotinate
437-74-1
US $0.00 / KG 1KG 98.5% 100kg/month WUHAN FORTUNA CHEMICAL CO., LTD
complamin contamex icotinicacid methoxylin,compd.withnicotinicacid nicotinicacid,compd.with3,7-dihydro-7-(2-hydroxy-3-((2-hydroxyethyl)methyl sadamin sk331a stenalgil teonicol vedrin xanthinolniacinate xavin 7-[2-hydroxy-3-(2-hydroxyethyl-methyl-amino)propyl]-1,3-dimethyl-purine-2,6-dione pyridine-3-carboxylic acid XANTINOL NICOTINATE XANTHINOL NICOTINATE 7-(2-hydroxy-3-((2-hydroxyethyl)methylamino)propyl)theophylline nicotinate XANTINOL NICOTINATEXANTHINOL NICOTINATE UV 3,7-Dihydro-7-[2-hydroxy-3-[(2-hydroxyethyl)methylamino]propyl]-1,3-dimethyl-1H-purine-2,6-dione (1:1) 7-[2-Hydroxy-3-[N-(2-hydroxyethyl)-N-methylamino]propyl]-1,3-dimethylxanthine pyridine-3-carboxylate 7-[2-Hydroxy-3-[N-methyl-N-(2-hydroxyethyl)amino]-propyl]-theophylline nicotinate 7-[3-(Methyl-2-hydroxyethylamino)-2-hydroxypropyl)]theophylline nicotinate 7-[2-hydroxy-3-[2-hydroxyethyl(methyl)amino]propyl]-1,3-dimethyl-purine-2,6-dione 7-[2-hydroxy-3-[2-hydroxyethyl(methyl)amino]propyl]-1,3-dimethylpurine-2,6-dione 7-[2-hydroxy-3-[2-hydroxyethyl(methyl)amino]propyl]-1,3-dimethyl-xanthine Nicotinic acid - 7-{2-hydroxy-3-[(2-hydroxyethyl)( methyl)amino]propyl}-1,3-dimethyl-3,7-dihydro-1H-p Nicotinic acid - 7-{2-hydroxy-3-[(2-hydroxyethyl)( methyl)amino]propyl}-1,3-dimethyl-3,7-dihydro-1H- Xanthinol Standard Nicotinic acid - 7-{2-hydroxy-3-[(2-hydroxyethyl)-(methyl)amino]propyl}-1,3-dimethyl-3,7-dihydro- 7-(2-Hydroxy-3-((2-hydroxyethyl)(methyl)amino)propyl)-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione amino)propyl)-1,3-dimethyl-1h-purine-2,6-dione angiomin complamex 7-(2-hydroxy-3-((2-hydroxyethyl)methylamino)propyl)theophyllinecompd.withn 7-(3-(n-(2-hydroxyethyl)amino)-2-hydroxypropyl)thiophyllinenicotinate 7-[3-[(2-Hydroxyethyl)methylamino]-2-hydroxypropyl]theophyllinenicotinate Xantinol Nicotinate(Xanthinol Nicotinate) Xanthiinol Nicotinate nicotinic acid - 7-{2-hydroxy-3-[(2-hydroxyethyl)(methyl)amino]propyl}-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione (1:1) Xanthinol nicotinate USP/EP/BP 7-[2-hydroxy-3-[2-hydroxyethyl(methyl)amino]propyl]-1,3-dimethylpurine-2,6-dione,pyridine-3-carboxylic acid Xanthinol nicotinate,437-74-1 7-(2-Hydroxy-3-((2-hydroxyethyl)(methyl)amino)propyl)-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione nicotinate 437-74-1 207-115-7 C19H26N6O6 C13H21N5O4C6H5NO2 Alphabetic Analytical Chromatography Product Catalog Analytical Standards 437-74-1