Identification | Back Directory | [Name]
Mesaconitine | [CAS]
2752-64-9 | [Synonyms]
NSC 77210 MESACONITINE Mesaaconitine Japaconitine A Japaconitine B MESACONITINE(SH) MESACONITINE(AS) Mesaconitine USP/EP/BP N-Desethyl-N-Methylaconitine Mesaconitine Solution, 100ppm MESACONITINE, 98% (PRIMARY STANDARD) Mesaconitine, 98%, from Aconitum carmichaeli Debeaux (1-alpha,3-alpha,6-alpha,14-alpha,15-alpha,16-beta)-8-acetate14-benzoat 13,14,15-pentol,1,6,16-trimethoxy-4-(methoxymethyl)-20-methyl-aconitane-8 1α,6α,16β-Trimethoxy-4-methoxymethyl-20-methylaconitane-3α,8,13,14α,15α-pentol 8-acetate 14-benzoate 4-(Methoxymethyl)-20-methyl-1α,6α,16β-trimethoxyaconitane-3α,8,13,14α,15α-pentol 8-acetate 14-benzoate (1a,3a,6a,14a,15a,16β)-1,6,16-Trimethoxy-4-(methoxymethyl)-20-methyl-aconitane-3,8,13,14,15-pentol 8-acetate 14-benzoate (1α,3α,6α,14α,15α,16β)-1,6,16-TriMethoxy-4-(MethoxyMethyl)-20-Methyl-aconitane-3,8,13,14,15-pentol 8-Acetate 14-Benzoate Aconitane-3,8,13,14,15-pentol, 1,6,16-trimethoxy-4-(methoxymethyl)-20-methyl-, 8-acetate 14-benzoate, (1α,3α,6α,14α,15α,16β)- Aconitane-3,8,13,14,15-pentol, 1,6,16-trimethoxy-4-(methoxymethyl)-20-methyl-, 8-acetate 14-benzoate, (1alpha,3alpha,6alpha,14alpha,15alpha,16beta)- | [EINECS(EC#)]
220-397-6 | [Molecular Formula]
C33H45NO11 | [MDL Number]
MFCD00210528 | [MOL File]
2752-64-9.mol | [Molecular Weight]
631.71 |
Chemical Properties | Back Directory | [Melting point ]
208-209 °C | [Boiling point ]
708.7±60.0 °C(Predicted) | [density ]
1.39±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,2-8°C | [pka]
12.14±0.70(Predicted) |
Hazard Information | Back Directory | [Description]
The structure of this aconitine alkaloid has now been elucidated and shown to be
that given above. | [Chemical Properties]
White Solid | [Uses]
An Aconitine (A189875) analog. Aconitine alkaloid pharmacokinetic analgesic. A highly poisonous, neurotoxic alkaloid. | [Definition]
ChEBI: Mesaconitine is a diterpenoid. | [References]
Jacobs, Pelletier, Chern. & Ind., 591 (1960)
Furner, Jeschka, Gibson,J. Arner. Chern. Soc., 82,5182 (1960) |
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