Phylloquinone
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Phylloquinone
structure -
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CAS No:
84-80-0
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Formula:
C31H46O2
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Chemical Name:
Phylloquinone
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Synonyms:
1,4-Naphthalenedione,2-methyl-3-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecen-1-yl]-;Phylloquinone;1,4-Naphthalenedione,2-methyl-3-(3,7,11,15-tetramethyl-2-hexadecenyl)-,[R-[R*,R*-(E)]]-;1,4-Naphthalenedione,2-methyl-3-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl]-;2-Methyl-3-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecen-1-yl]-1,4-naphthalenedione;Antihemorrhagic vitamin;Mephyton;2-Methyl-3-phytyl-1,4-naphthoquinone;Mono-Kay;Phytomenadione;Phytonadione;Phytylmenadione;Vitamin K1(20);α-Phylloquinone;Konakion;trans-Phylloquinone;2′,3′-trans-Vitamin K1;Synthex P;Kephton;Kinadion;Monodion;Combinal K1;Kativ N;AquaMEPHYTON;Kaywan;Phylloquinone K1;Phytylmenaquinone;Pediatrico;Orakay;Veta K1;Veda K1;NSC 270681;Kanakion;Amri-K;Haemokion;Kenadion;Reconval;10485-69-5;15973-57-6;50926-17-5
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CAS No:
Description
It appears as yellow to orange transparent viscous liquid and is odorless with the relative density being 0.967 and the refractive index being nD251.525~1.528. It is easily soluble in chloroform, ether and vegetable oil, slightly soluble in ethanol and insoluble in water. It is easily to be decomposed when exposed to light and with being decomposed upon being heated to 120 ℃. Yellow Oil Phylloquinone is an odorless yellow viscous oil or crystals.
Characteristics
34.1
9.3
viscous liquid
0.964 g/cm3 @ Temp: 25 °C
-20 °C
140-145 °C @ Press: 1 x 10-3 Torr
>230 °F
1.527
Miscible with dehydrated alcohol, acetone, petroleum ether, hexane, dioxane, chloroform, ether,benzene and vegetable oils. Immiscible with water.
2-8°C
D25 -0.28° (dioxane)
Odorless
SOLN OF 1 PART VIT K1 & 20 PARTS ALC IS NEUTRAL TO LITMUS
Safety Information
UN1170 - class 3 - PG 2 - Ethanol, solution
2
36/37/38
26-37/39-24/25
QJ5800000
Xi
Phytonadione is stable to heat and moisture and may be autoclaved.
P273, P501
H413
Phylloquinone Use and Manufacturing
In the presence of zinc, o-methylnaphthoquinone and acetic anhydride are reduced and acetylated to form acetylated menadione; then hydrolyzed in ammonia, and then catalyzed by boron trifluoride in ether to condense with plant alcohols to obtain dihydrovitamin K1 ; Finally, the product is obtained by hydrolysis, oxidation, purification and refining.
Occurs widely in green plants, algae, photosynthetic bacteria.
Drug Function and Efficacy
Can form prothrombin to maintain normal blood coagulation function. When it is deficient, it causes prothrombin deficiency bleeding.
Registered Holders
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SUNNY PHARMTECH INC
Active
United States
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ENALTEC LABS PRIVATE LTD
Active
United States
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BIOPHORE INDIA PHARMACEUTICALS PVT LTD
Active
United States
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