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Menadione

Menadione Structure
CAS No.
58-27-5
Chemical Name:
Menadione
Synonyms
VITAMIN K3;VITAMIN K;VK3;2-METHYL-1,4-NAPHTHOQUINONE;Menadion;2-METHYL-1,4-NAPHTHAQUINONE;Aquakay;Aquinone;Vitmin K3;menadione (k3)
CBNumber:
CB4494726
Molecular Formula:
C11H8O2
Molecular Weight:
172.18
MOL File:
58-27-5.mol
MSDS File:
SDS
Modify Date:
2024/7/1 9:17:29

Menadione 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. room temp
solubility oil: soluble
form crystalline
color yellow
Odor Slight odor
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
LogP 2.200
CAS DataBase Reference 58-27-5(CAS DataBase Reference)
NIST Chemistry Reference Menadione(58-27-5)
EPA Substance Registry System Menadione (58-27-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H302-H315-H319-H334-H335-H410
Precautionary statements  P261-P264-P273-P301+P312-P302+P352-P305+P351+P338
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
HS Code  29147000
Toxicity LD50 orally in mice: ~0.5 g/kg (Molitor, Robinson)
NFPA 704
1
2 1

Menadione price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) M9429 Menadione meets USP testing specifications 58-27-5 25G ₹4026.9 2022-06-14 Buy
Sigma-Aldrich(India) PHR1411 Menadione Pharmaceutical Secondary Standard; Certified Reference Material 58-27-5 500MG ₹8281.13 2022-06-14 Buy
Sigma-Aldrich(India) M9429 Menadione meets USP testing specifications 58-27-5 100G ₹7501.73 2022-06-14 Buy
Sigma-Aldrich(India) M5625 Menadione crystalline 58-27-5 25G ₹5163.53 2022-06-14 Buy
Sigma-Aldrich(India) M5625 Menadione crystalline 58-27-5 100G ₹13140 2022-06-14 Buy
Product number Packaging Price Buy
M9429 25G ₹4026.9 Buy
PHR1411 500MG ₹8281.13 Buy
M9429 100G ₹7501.73 Buy
M5625 25G ₹5163.53 Buy
M5625 100G ₹13140 Buy

Menadione Chemical Properties,Uses,Production

Description

Vitamin K is a general term referring to a group of naphthoquinone derivatives required in the diet for blood clotting. Menadione is a fat-soluble vitamin that is essential for blood clotting. It is destroyed by irradiation during processing but has no appreciable loss during storage. It occurs in spinach, cabbage, liver, and wheat bran.

Chemical Properties

Bright-yellow crystals with a very faint acrid odour. Insoluble in water; soluble in benzene (1 g/10 mL), ethanol (1 g/60 mL), and vegetable oils (1g/50 mL); moderately soluble in carbon tetrachloride and chloroform. Stable in air; decomposed by sunlight; destroyed by alkalis and reducing agents.

Physical properties

Appearance: phylloquinone is a yellow oil at room temperature, but the other vitamers K are yellow crystals. Solubility: the vitamers K and MK and most forms of menadione are insoluble in water, slightly soluble in ethanol, and readily soluble in ether, chloroform, fats, and oils. Stability: the vitamers K are sensitive to light and alkali, but are relatively stable to heat and oxidizing environments.
Menadione, the formal parent compound of the menaquinone series does not occur naturally but is a common synthetic form called menadione (2-methyl-1,4- naphthoquinone). This compound forms a water-soluble sodium bisulfite addition product, menadione sodium bisulfite, whose practical utility is limited by its instability in complex matrices such as feeds. However, in the presence of excess sodium bisulfite, it crystallizes as a complex with an additional mole of sodium bisulfite (i.e., menadione sodium bisulfite complex), which has greater stability, therefore, is used widely as a supplement to poultry feeds. A third water-soluble compound is menadione pyridinol bisulfite (MPB).

Uses

Menadione is precursor to verious types of Vitamin K. It is of industrial importance as an intermediate in the synthesis of phylloquinone, and salts of its bisulfite adduct are used as stabilized forms in the animal feed industry. Commercially significant forms are menadione sodium bisulfite and menadione dimethyl pyrimidinol. Used as a micronutrient for livestock and pet foods.

Application

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. It is being incorporated into cosmetic preparations, particularly those used for treating dark circles. It could also be used in acne products, and there are studies underway on its efficacy for the treatment of spider veins.

Indications

Vitamin K activity is associated with several quinones, including phylloquinone (vitamin K1), menadione (vitamin K3), and a variety of menaquinones (vitamin K2). These quinones promote the synthesis of proteins that are involved in the coagulation of blood.These proteins include prothrombin, factor VII (proconvertin), factor IX (plasma thromboplastin). The vitamin K quinones are obtained from three major sources.Vitamin K is present in various plants, especially green vegetables. The menaquinones that possess vitamin K2 activity are synthesized by bacteria, particularly gram-positive organisms; the bacteria in the gut of animals produce useful quantities of this vitamin.Vitamin K3 is a chemically synthesized quinone that possesses the same activity as vitamin K1.

Definition

ChEBI: Menadione is a member of the class of 1,4-naphthoquinones that is 1,4-naphthoquinone which is substituted at position 2 by a methyl group. It is used as a nutritional supplement and for the treatment of hypoprothrombinemia. It has a role as a nutraceutical, a human urinary metabolite, an angiogenesis inhibitor, an EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor and an antineoplastic agent. It is a member of 1,4-naphthoquinones and a vitamin K.

Preparation

Menadione can be prepared by oxidizing 2-methylnaphthalene with chromic acid or hydrogen peroxide.

General Description

Menadione is a prothrombogenic compound and belongs to the Vitamin K class of compounds, which are necessary for the biosynthesis of prothrombin and other blood clotting factors. It is used as a model quinone in cell culture and in vivo investigations. It is obtained as a catabolic product of phylloquinone and circulating precursor of tissue menaquinone-4 in rats.

Hazard

Irritant to skin and mucous membranes, especially the alcoholic solution.

Pharmacology

The typical role of vitamin K is to maintain normal blood coagulation function. Its role is related to the metabolic processes.

Clinical Use

Vitamin K deficiency results in increased bleeding time. This hypoprothrombinemia may lead to hemorrhage from the gastrointestinal tract, urinary tract, and nasal mucosa. In normal, healthy adults, deficiency is rare. The two groups at greatest risk are newborn infants and patients receiving anticoagulant therapy; hypoprothrombinemia preexists in these two groups. Any disease that causes the malabsorption of fats may lead to deficiency. Inhibition of the growth of intestinal bacteria from extended antibiotic therapy will result in decreased vitamin K synthesis and possible deficiency.

Side effects

Toxicity of vitamin K has not been well defined. Jaundice may occur in a newborn if large dosages of vitamin K are given to the mother before birth. Although kernicterus may result, this can be prevented by using vitamin K.

Safety Profile

Poison by ingestion, intraperitoneal, and subcutaneous routes. Experimental teratogenic effects. Questionable carcinogen with experimental tumorigenic data. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Recrystallise it from 95% EtOH, or MeOH after filtration. It forms bright yellow crystals which are decomposed by light. Its solubility in EtOH is 1.7% and in *C6H6 it is 10%. It IRRITATES mucous membranes and skin. [Fieser J Biol Chem 133 391 1940, Beilstein 7 IV 2430.]

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