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12001-79-5

12001-79-5 Structure

12001-79-5 Structure
IdentificationBack Directory
[Name]

VITAMIN K1
[CAS]

12001-79-5
[Synonyms]

C01628
VITAMIN K
Synkavite
VITAMIN K1 USP23
Vitamin K substances
2-methyl-3-[(E)-3,7,11,15-tetramethylhexadec-2-enyl]naphthalene-1,4-dione
[EINECS(EC#)]

201-564-2
[Molecular Formula]

C31H46O2
[MDL Number]

MFCD00001683
[MOL File]

12001-79-5.mol
[Molecular Weight]

450.7
Chemical PropertiesBack Directory
[Melting point ]

−20 °C(lit.)
[density ]

0.984 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.527(lit.)
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
[form ]

viscous liquid
[color ]

Light yellow to yellow
[LogP]

10.305 (est)
[CAS DataBase Reference]

12001-79-5
[IARC]

3 (Vol. 76) 2000
[EPA Substance Registry System]

Vitamin K (12001-79-5)
Safety DataBack Directory
[WGK Germany ]

2
[RTECS ]

QJ5800000
[F ]

1-8-10
[TSCA ]

TSCA listed
[Safety Profile]

Moderately toxic by subcutaneous route. An experimental teratogen. When heated to decomposition it emits acrid smoke and irritating fumes.
[Toxicity]

mouse,LD50,subcutaneous,700mg/kg (700mg/kg),Arzneimittel-Forschung. Drug Research. Vol. 8, Pg. 25, 1958.
Hazard InformationBack Directory
[Definition]

ChEBI:2-methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)naphthalene-1,4-dione is a member of 1,4-naphthoquinones.
[Biological Functions]

Both vitamins K3 and K4 may produce hyperbilirubinemia and kernicterus in neonates as well as hemolysis in neonates and glucose-6-phosphate–deficient patients. In fact, the only advantage of vitamins K3 and K4 over vitamin K1 is that whereas absorption of vitamin K1 requires the presence of bile, absorption of vitamins K3 and K4 does not, because they are absorbed via a passive process directly from the intestine. This may be a slight advantage for patients with cholestasis or severe pancreatic dysfunction. Only vitamin K1, however, is appropriate therapy for bleeding associated with warfarin and superwarfarin anticoagulation. Vitamin K2 is not used therapeutically.
[Mechanism of action]

Vitamin K antagonists, such as warfarin, produce their effect on blood coagulation by interfering with the cyclic interconversion of vitamin K and vitamin K 2,3-epoxide. Vitamin K is an essential cofactor necessary for the posttranslational carboxylation of the glutamic acid residues on the N-terminal portions of the specific clotting factors (II, VII, IX, and X) and anticoagulant proteins, such as protein C. This γ-glutamyl carboxylation results in a new amino acid, γ-carboxyglutamate, which through chelation of calcium ions causes the proteins to undergo a conformational change. This change in tertiary structure allows the four vitamin K–dependent clotting factors to become activated and bind to the negatively charged phospholipid membranes during clotting cascade activation.
[Pharmacokinetics]

The half-life of vitamin K1 is quite short—only 1.7 hours via the intravenous route and 3–5 hours via the oral route. When given orally, vitamin K1 is absorbed directly from the proximal small intestine in an energy-dependent and saturable process that requires the presence of bile salts. These kinetic features argue for administration in divided doses rather than larger, single daily doses. The typical starting point for adults with drug-induced hypoprothrombinemia is 2.5 to 10 mg of vitamin K1 orally, repeating in 12 to 48 hours if needed. In cases of ingestion of long-acting superwarfarin rodenticides (e.g., brodifacoum), therapy may be 125 mg/day for weeks or months. Practically speaking, because vitamin K1 is dispensed as 5-mg tablets, superwarfarin-poisoned patients may require 10 to 30 tablets every 6 hours.
[Clinical Use]

Vitamin K1 (phytonadione, Mephyton) is the form of vitamin K most often used therapeutically. Vitamin K1 is safe for use in infants, pregnant women, and patients with glucose-6-phosphate deficiency.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

VITAMIN K1(12001-79-5)1HNMR
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