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Postion:Product Catalog >API>Vitamins and Minerals medicines>Vitamin C drugs>Menadione
Menadione
  • Menadione

Menadione

Price $1
Package 1KG
Min. Order: 1G
Supply Ability: 100KG
Update Time: 2019-07-06

Product Details

Product Name: Menadione CAS No.: 58-27-5
Min. Order: 1G Purity: 98%
Supply Ability: 100KG Release date: 2019/07/06

AD68

Menadione Basic information
Chemical properties Application Production
Product Name: Menadione
Synonyms: usafek-5185;VitaminK0;β-Methyl-1,4-naphthoquinone;Menadione (1.05793);MENADIONE, USP;MENADIONE (K3) 1000MG NEAT;(MENADIONE)VITAMIN K3, 98+% USP;VITAMIN K3(FEEDSTUFF GRADEMSB96)
CAS: 58-27-5
MF: C11H8O2
MW: 172.18
EINECS: 200-372-6
Product Categories: Biochemistry;Vitamins;Nutritional fortification substances;Vitamins and derivatives;Vitamin Ingredients;Miscellaneous Compounds;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;RUMENSIN;Isolabel;Other APIs;Inhibitors;feeding additive raw materials
Mol File: 58-27-5.mol
Article illustration
 
Menadione Chemical Properties
Melting point  105-107 °C(lit.)
Boiling point  262.49°C (rough estimate)
density  1.1153 (rough estimate)
refractive index  1.5500 (estimate)
storage temp.  Store at RT.
solubility  oil: soluble
form  crystalline
color  yellow
Water Solubility  INSOLUBLE
Sensitive  Light Sensitive
Merck  14,5831
BRN  1908453
Stability: Stable. May be light sensitive. Incompatible with strong oxidizing agents.
InChIKey MJVAVZPDRWSRRC-UHFFFAOYSA-N
CAS DataBase Reference 58-27-5(CAS DataBase Reference)
NIST Chemistry Reference Menadione(58-27-5)
EPA Substance Registry System 1,4-Naphthalenedione, 2-methyl-(58-27-5)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38-43
Safety Statements  26-36-37/39-24
WGK Germany  3
RTECS  QL9100000
8
TSCA  Yes
HazardClass  IRRITANT
Hazardous Substances Data 58-27-5(Hazardous Substances Data)
Toxicity LD50 orally in mice: ~0.5 g/kg (Molitor, Robinson)
Menadione Usage And Synthesis
Chemical properties It appears as white crystalline or crystalline powder, being almost odorless and hygroscopic. Its color will change in case of light. It is easily soluble in water, slightly soluble in ethanol, but insoluble in ether and benzene.
Application Biochemical research; clinical drugs belong to fat-soluble vitamins; it is clinically used as a hemostatic drug.
Vitamin K3 is mainly used as poultry feed enhancer at a dosage of 1-5mg/kg.
The goods can have addition reaction with sodium bisulfite to generate vitamin K3.
VK3. Used as raw material of feed additives; it can mainly promote the liver synthesis of prothrombin in livestock and poultry, and promote the liver synthesis of plasma coagulation factors as a hemostatic agent.
Traits: bright yellow crystal with very spicy smell. It is stable in the air and will be decomposed in sunlight. 1G can be dissolved in about 60ml ethanol, 10ml benzene and 50 ml vegetable oil. It is soluble in chloroform and carbon tetrachloride but insoluble in water. The ethanol solution was neutral to litmus paper. The solution will not be decomposed even when heated to 120 °C. It will be destroyed upon treatment with alkali and reducing agent. It is toxic with the half lethal dose (mouse, oral) being about 500 mG/kG. It is irritating. Its commodities still include sodium bisulfite manaquinone, appearing as white crystalline powder. It has no smell or with slightly special smell. It has hygroscopicity. It undergoes decomposition in case of light to turn into yellow or purple color. It is easily soluble in water, slightly soluble in ethanol, but almost insoluble in ether and benzene. Application: biochemical research
Production There are two production processes. 1. Methyl naphthalene is obtained from the oxidization of chromic anhydride. 2-methyl naphthalene is dissolved in glacial acetic acid, stirred and cooled to temperature below 40 ℃. Slowly add the mixture of chromic anhydride and the same amount of water so that the temperature can be maintained at 35-40 ℃. After the completion of the addition, maintain the temperature at 40 ℃ for 0.5 h, the temperature was then raised to 70 ℃ for 45min, and further heated to 85 ℃ for 15min. Pour the reactants into a lot of water and stir continuously to precipitate out the 2-naphthoquinone. Filter and rinse the filter cake repeatedly with water, until the aqueous solution has no sour. Filter to get the 2-menenoquinone with a yield of 51%. 2-methyl naphthalene can also be made from sodium dichromate and potassium dichromate with the oxidation yield being roughly the same. 2. Cyclohexanone has cyclization reaction with butadiene to get 2-methyl naphthalene hydroquinone, followed by oxidation with chromic acid to obtain the final product. Dissolve the toluquinone in glacial acetic acid; send the butadiene to the required amount at temperature below 20 ℃; stand for 20 hours; heat to release the remaining butadiene and continue to heat to about 110 °C for refluxing of 3 hours. Then recycle 30% of glacial acetic acid through vacuum distillation and cooled to temperature below 40 ℃; slowly add the mixture of chromic acid and the same amount of water so that the temperature is maintained at 65-70 ℃. After the completion of the addition, maintain the temperature at 70-80 degree for 1h to obtain the menadione.
O-methyl naphthoquinone is used as raw material. It undergoes oxidation with glacial acetic acid and chromic anhydride, followed by addition with sodium bisulfite in ethanol to derive it.
Chemical Properties Bright yellow crystals
Uses Precursor to verious types of Vitamin K. Used as a micronutrient for livestock and pet foods.
Uses prothrombogenic agent
Uses antibacterial
Uses The primary known function of vitamin K is to assist in the normal clotting of blood, but it may also play a role in normal bone calcification.
Definition ChEBI: A member of the class of 1,4-naphthoquinones that is 1,4-naphthoquinone which is substituted at position 2 by a methyl group.
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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