Methylamin-manufacture,factory,supplier from China

(Total 24 Products for Methylamin)
Aspartic acid, also known as aspartic acid, is a α-amino acid, the L-isomer of aspartic acid is one of the 20 protein amino acids, that is, the building unit of protein, its codons are GAU and GAC. It is an acidic amino acid with glutamic acid. It belongs to one of the non-essential amino acids in the human body. Aspartic acid is ubiquitous in biosynthesis. It is a synthetic precursor of amino acids such as lysine, threonine, isoleucine, methionine and purine and pyrimidine bases in living organisms.
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1.3-Butanediol is an organic compound with a molecular formula of C4H10O2, mainly used in the preparation of polyester resin, polyurethane resin, plasticizer, etc., and also used as a humidifier and softener for textiles, paper and tobacco.Chinese Name: 1,3-ButanediolChinese aliases: 1,3-Dihydroxybutane; (±)-1,3-ButanediolEnglish alias: Butanediol; butane-1,3-diol; (3S)-butane-1,3-diol; (3R)-butane-1,3-diolCAS:107-88-0EINECS:203-529-7FEMA registration number: 2842Physical and chemical indicatorsAppearance: colorless, viscous liquid.Melting point (°C): <-54Boiling point (°C): 207°C at 760 mm
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Fields of applicationPurpose 1It is suitable for vitamin B1 deficiency, has the function of maintaining normal glucose metabolism and nerve conduction, and is also used for the adjuvant treatment of dyspepsia and neuritisPreparation method:Method 1Thiamine hydrochloride is usually obtained by condensation, hydrolysis, neutralization, oxidation, and acidification of excess acetamidine hydrochloride with α-dimethoxy β-methoxypropionitrile.Upstream and downstream product informationUpstream raw materialsEthanol, hydrogen peroxide, dimethyl sulfate, ethyl chlorosulfonate, acrylonitrile, carboxylat
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Pharmacological actionSince the discovery that long-acting local anesthetics can induce cardiac arrest, people have been looking for safer alternatives with less fat solubility. Ropivacaine is such a new long-acting amide local anesthetic, which has a long duration of action and has anesthetic and analgesic effects. Its pharmacological characteristics are low cardiotoxicity, sensory block and motor block are clearly separated, and it has peripheral vasoconstriction effect.
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Pharmacology and toxicologyWhen the plasma concentration exceeds 5 μg·mL-1, convulsions can occur, and at low doses, it can promote the outflow of K+ in myocardial cells, reduce the auto-discipline of the myocardium, and have anti-ventricular arrhythmic effect; At therapeutic doses, there is no significant effect on the electrical activity of cardiomyocytes, atrioventricular conduction and contraction of myocardium; Further increase in blood concentration can cause slowing of cardiac conduction velocity, atrioventricular block, inhibition of myocardial contractility and decrease of cardiac out
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Quality standardsOff-white to light yellow crystalline appearanceContent 299% (HPLC)Melting point 216-220°C(s2C)Moisture S21.5%Ignition residue S0.2%The ethanol water dissolution test (thousand products) is qualifiedUses: used in pharmaceuticals, biological reagents, dyes, can also be used to synthesize 5,7-dimeryl flavonoids.As a medicine, resorcinol directly acts on the smooth muscle of the gastrointestinal tract and genitourinary tract, and is a prophilic non-atropine non-sinosynergine pure smooth muscle antispasmodic drug Compared with other smooth muscle spasmodics, resorcinol is characte
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Chemical and physical properties of benzophenone hydrazoneDensity 1.1±0.1 g/cm3Boiling point 328.0±11.0 °C at 760 mmHgmelting point 95-98 °C(lit.)Molecular Formula C13H12N2Molecular weight 196.248Flash point 152.1±19.3 °CExact mass 196.100052PSA 38.38000LogP 2.79Appearance: White crystalline powderVapor pressure 0.0±0.7 mmHg at 25°CThe refractive index is 1.584Storage conditionsProtect from light, cool and dry place, sealed and storedstabilityStable at room temperature and pressure, white crystalline powder.MolecularMolecular property data:1. Molar refractive index: 62.322.
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English name: FebuxostatDescription: light green to off-white powder.Uses: Oxidase and dehydrogenase inhibitors. Used to treat hyperuricemia (gout).Treatment: Febuxostat is a new generation of Huangyuanling oxidase inhibitor developed by Teijin Corporation of Japan, clinically used for the treatment of hyperuritic acid (gout), the structure is completely different from the Huang Blao Ling oxidase inhibitor drug developed 40 years ago, it is a new and efficient non-original Huang Ling oxidase selective inhibitor. Yellow Ticket Ridge oxidase is a key enzyme that promotes uric acid production.
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Pharmacology and toxicologyWhen the plasma awareness exceeds 5 μg·mL-1, convulsions can occur, and at low doses, it can promote the outflow of K+ in myocardial cells, minimize the auto-discipline of the myocardium, and have anti-ventricular arrhythmic effect; At therapeutic doses, there is no full-size impact on the electrical endeavor of cardiomyocytes, atrioventricular conduction and contraction of myocardium; Further enlarge in blood awareness can reason slowing of cardiac conduction velocity, atrioventricular block,
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TriacetateGlyceryl triacetate is an organic compound with a C9H14O6 molecular formula, colorless and odorless oily liquid, miscible with ethanol, ether, chloroform and benzene, slightly soluble in water and carbon disulfide. Used as cigarette filter binder and fragrance fixative, solvent, toughening agent. And can be used in cosmetics, casting, medicine, dyes and other industries. This product is non-toxic and non-irritating.Production methodIt is obtained by glycerol and acetate. After preheating glycerol to 50-60 ° C, acetic acid is added; Benzene and sulfuric acid.
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n-propanol, also known as 1-propanol, is an organic compound with a simple structural formula of CH3CH2CH2OH, a molecular formula of C3H8O, and a molecular weight of 60.10. At room temperature and pressure, n-propanol is a transparent colorless liquid with a strong musty smell similar to external alcohol, soluble in water, ethanol and ether. Generally, propionaldehyde is obtained by the synthesis of ethylene by carbonyl group, and then reduced to obtain.
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Sodium gluconate is a type of natural matter, chemical components C6H11NaO7, in the enterprise is very extensively used, sodium gluconate can be used in construction, fabric printing and dyeing and metallic floor cure and water remedy industries as environment friendly chelating agent, metal floor cleansing agent, glass bottle cleansing agent, electroplating industrial aluminum oxide coloring, in the concrete enterprise as a excessive effectivity
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CAS:26412-87-3Chinese Name: Thiopidine trioxide Chinese synonyms: compounds of thiopidine trioxide; sulfur trioxide-pyridine complex; Pyridine sulfur trioxide; Thiopidine trioxide; Thiopidine trioxide complex; Synthesis of thiophorine trioxide; Sulfur trioxide yridine complex; Sulfurtrioxypyridine complicated [2]English name: Pyridine sulfur trioxide English synonyms: Pyridine, compd.withsulfurtrioxide (1:1); Salfurtrioxidepyri-dinecomplex; Sulfurtrioxide,compd.withpyridine(1:1); (DIMETHYLAMINOMETHYL) STYRENE; VINYLBENZYLDIMETHYLAMINE; N,N-DIMETHYLVINYLBENZYLAMINE; POLY(4-V
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Cyclohexanone is an organic compound with the formula C6H10O , a saturated cyclic ketone with carbonyl carbon atoms included in a six-membered ring. Colorless transparent liquid with earthy smell, with mint smell when containing trace amounts of phenol. Impurities are light yellow, which develop color with the formation of impurities during storage time, and are water-white to gray-yellow, with a strong pungent odor. Mixed with air, the explosive pole is the same as open-chain saturated ketone.
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The appearance is colorless and crystalline, and it can be sublimated when it is exposed to light or discoloration in the air.Appearance trait: colorless crystal. Discoloration in case of air and light. Its solution turns tan in the air.
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Uroptrazine, additionally recognized as hexamethylenetetramine, has the system C6H12N4 and is an natural compound.It is listed in the "List of Hazardous Chemicals Prone to Explosion" [1] and managed in accordance with the "Measures for the Safety Management of Hazardous Chemicals that Can Be Made into Explosives"Toxicological dataAcute toxicity: LD50: 9200mg/kg (rat venous); 569mg/kg (mouse by way of mouth).Use of methenamine1.
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Chemical propertiesFormaldehyde and resorcinol react under alkaline conditions to form orange-red compounds, which are colorimetric at a maximum absorption wavelength of 460nm to detect low traces of formaldehyde in textile and clothing.Since resorcinol can undergo enol and ketone form tautomerism, it can react with ammonia as follows:Ketone reaction of resorcinolUnder the action of ammonia, m-phenyltriamine is obtained by reaction in ketone, and the amine is hydrolyzed in the aqueous solution of acid to obtain resorcinol.
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Sulfadiazine is an organic compound with a molecular formula of C10H10N4O2S, white or off-white crystals or powders, odorless, tasteless, and gradually darkened when exposed to light. Almost insoluble in water, soluble in boiling water (1:60), slightly soluble in ethanol and acetone, insoluble in chloroform and ether, soluble in dilute hydrochloric acid, sodium hydroxide solution or ammonia solution. Melting point 252~256 °C (simultaneous decomposition). Its sodium salt is white crystalline powder, odorless, slightly bitter taste. Gradient brownish upon light.
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Sulfadiazine is an natural compound with a molecular formulation of C10H10N4O2S, white or off-white crystals or powders, odorless, tasteless, and step by step darkened when uncovered to light. Almost insoluble in water, soluble in boiling water (1:60), barely soluble in ethanol and acetone, insoluble in chloroform and ether, soluble in dilute hydrochloric acid, sodium hydroxide answer or ammonia solution. Melting factor 252~256 °C (simultaneous decomposition).
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CAS No. 503615-07-4 Molecular formula C22H22N4O4 molecular weight 406.43EINECS No.
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Magnesium sulfate solution, volumetric laxatives and choleretic agents. It is used for catharsis, choleretic, duodenal drainage and local swelling.Ingredients BroadcastThe main component of this product is magnesium sulfate.It is a sterilized aqueous solution of magnesium sulfate. Magnesium sulfate (MgSO4.7H2O) should be 95.0%~105.0% of the labeled amount.Molecular formula: MgSO4·7H2OMolecular weight: 246.48Indications BroadcastVolumetric laxatives and choleretics.
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Hydrazine hydrate, additionally recognised as hydrazine hydrate, is a colorless and obvious oily liquid with a mild ammonia smell, smoke in humid air, and is exceedingly alkaline and hygroscopic.
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Hydrazine hydrate, also known as hydrazine hydrate, is a colorless and transparent oily liquid with a light ammonia smell, smoke in humid air, and is highly alkaline and hygroscopic.
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Uroptrazine, also known as hexamethylenetetramine, has the formula C6H12N4 and is an organic compound.It is listed in the "List of Hazardous Chemicals Prone to Explosion" [1] and controlled in accordance with the "Measures for the Safety Management of Hazardous Chemicals that Can Be Made into Explosives"Toxicological dataAcute toxicity: LD50: 9200mg/kg (rat venous); 569mg/kg (mouse by mouth).[3] Use of methenamineUsed as a curing agent for resins and plastics, catalyst and foaming agent for amino plastics, accelerator for rubber vulcanization (accelerator H), anti-shri
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Medicine intermediate refers to a compound generated as an intermediate step in the process of synthetic drugs. It has high purity and activity, which can synthesize target drugs through further chemical reactions. Medicine intermediates are widely used in the pharmaceutical industry, covering multiple fields. The classification of pharmaceutical intermediates and its application areas will be introduced below.1. Carboxylic acid intermediate:The intermediate of the carboxylic acid refers to the compound of the carboxylic acid group, and the common ones are benzoic acid and propylic acid.
May 13, 2020. Pharmaceutical intermediate body fluorine customized. Pharmaceutical fluorine: colorless liquid. The melting point -42 ℃. Boiling point 85 ° C. Refractive index (ND20) 1.4650. Relators (D420) 1.024. Insuvenate in water and mixes with ethanol, ether, acetone, and benzene. Apineine reacts through Schiemann (G. Schiemann).Ah. After the aniline was descended to -8 ° C after 31%hydrochloride, and the sodium nitrite solution was nitroded.
I. Overview of chemical and pharmaceutical intermediatesChemical pharmaceutical intermediates are a very important part of the pharmaceutical industry, referring to raw materials or semi-finished products in the pharmaceutical industry. These substances undergo a series of chemical reactions to eventually form pharmaceutical products. These chemicals usually exist in liquid or solid form and belong to various types of organic compounds such as acids, alcohols, carboxylic acids, phenols, cork and so on.
Shandong is one of the important pharmaceutical production bases in the country, and the production production is relatively concentrated. The treatment of Shandong Pharmaceutical Intermediate waste is essential for protecting the environment, human health, and sustainable enterprise. This article will discuss how to properly handle waste in the production of Shandong pharmaceutical intermediates.First, reasonable classification and storage wasteReasonable classification and storage waste are the first step in waste treatment.
April 23, 2020. Customized in the middle of Shandong Pharmaceutical. The so -called Shandong pharmaceutical intermediate is actually some chemical raw materials or chemical products for drug synthesis process. This kind of chemical product does not require the production license of drugs. It can be produced in ordinary chemical plants. As long as it reaches some levels, it can be used for the synthesis of drugs.There are more than 2,000 raw materials and intermediates that need to be matched with chemicals each year, with more than 2.5 million tons.
Intermediate production of chemical medicine is a work involving a large number of chemicals. If it is not managed and controlled correctly, it may bring serious risks and pollution to the environment. In order to reduce environmental risks in the production of chemical medicine, we need to improve and control from the following aspects.First, establish a scientific and standardized production process. The production of chemical medicine needs to go through multiple steps and reactions. Each step needs to carefully evaluate and formulate corresponding operating procedures.