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lannaconitine

lannaconitine Structure
CAS No.
32854-75-4
Chemical Name:
lannaconitine
Synonyms
LAPPACONITINE;Lannaconitine;Aconitum extract;(+)-Lappacontine;(+)-Lappaconitine;N-Acetylpuberanidine;(+)-Lappaconitine >90%;Giant Typhonium Rhizome;Aconitum kusnezoffii Reichb;acetyl-10-deoxysepaconitine
CBNumber:
CB3235290
Molecular Formula:
C32H44N2O8
Molecular Weight:
584.7
MOL File:
32854-75-4.mol
MSDS File:
SDS
Modify Date:
2024/8/1 17:24:36

lannaconitine Properties

Melting point 217-218°
alpha D18 +27° (chloroform)
Boiling point 641.72°C (rough estimate)
Density 1.1897 (rough estimate)
refractive index 1.6260 (estimate)
storage temp. Store at 2-8°C, protect from light
solubility Chloroform: 30 mg/ml
form A solid
pka 12.55±0.70(Predicted)
Stability Hygroscopic

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P270-P301+P310-P321-P330-P405-P501
Toxicity LD50 in mice (mg/kg): 6.9 i.v.; 9.1 i.p.; approx 20 orally (Dybing)
NFPA 704
0
3 0

lannaconitine Chemical Properties,Uses,Production

Description

A highly toxic aconitine alkaloid present in Aconitum leucostomum and A. septentrionale Koelle, lappaconitine crystallizes in hexagonal tablets for whichtwo melting points have been recorded. It has [α]D + 22.3° (C6H6) or [α]18D + 27.0° (CHC1 3). The early view that a methylimino group is present has been shown to be erroneous. No crystalline salts are known but the diacetyl derivative forms colourless crystals, m.p. l25-7°C. The base is only sparingly soluble in H20 and most organic solvents, but dissolves readily in CHC1 3.
Boiling the alkaloid with dilute H2S04 in a stream of H2 yields acetic acid and anthranoyllappaconine, C30H4207N2, which forms colourless rhombic tablets, m.p. 146-9°C;[α]25D + 22.07° (C6H6), giving a platinichloride tetrahydrate as brown needles, m.p. 300-31 O°C (dec.). When hydrolyzed with HCl, the base furnishes acetic and anthranilic acids and lappaconine, m.p. 96°C; [α]25D + 22.41°, giving a crystalline hydrochloride, m.p. 246-7°C and the aurichloride monohydrate, m.p. l26-7°C. Alkaline hydrolysis, on the other hand, furnishes lappaconine and lappaconitic acid (acetylanthranilic acid). From these observations, it is clear that only one hydroxyl group is associated with an acyl group in the molecule.
Pharmacologically, lappaconitine is toxic although its action is less pronounced than that of aconitine (q.v.). Toxic doses produce respiratory paralysis and have a direct action upon the heart often terminating in ventricular fibrillation.

References

Schultze, Ulfert., Arch. Pharrn., 260,230 (1922)
Weidemann., Chern. Zentr., 1,603 (1923)
Khaimova et al., Tetrahedron Lett., 2711 (1964)
Structure:
Tel'nov, Yunusov, Yunusov., Khirn. Prir. Soedin., 6, 583 (1970)
Pharmacology:
Rosendahl., quoted by Boehm,!. BioI. Chern., 170,203 (1947)

lannaconitine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 208)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CRO Splendid Lab Private Limited 08048371921Ext 950 Pune, India 5 58 Inquiry
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lannaconitine Spectrum

(1a,14a,16b)-20-Ethyl-1,14,16-trimethoxyaconitane-4,8,9-triol 4-(2-acetylamino)benzoate) (1α,14α,16β)-20-Ethyl-1,14,16-trimethoxyaconitane- 4,8,9-triol4-[2-(acetylamino)benzoate] Aconitane-4,8,9-triol, 20-ethyl-1,14,16-trimethoxy-, 4-(2-acetylamino)benzoate, (1-alpha,14-alpha,16-beta) 20-Ethyl-1α,14α,16β-trimethoxyaconitane 4,8,9-triol 4-[2-(acetylamino)benzoate] 20-Ethyl-1α,14α,16β-trimethoxyaconitane-4,8,9-triol 4-[2-(acetylamino)benzoate] N-Acetylpuberanidine Lannaconitine Aconitum kusnezoffii Reichb LAPPACONITINE Aconitum extract ,(1-alpha,14-alpha,16-beta)- 8,9-triol,20-ethyl-1,14,16-trimethoxy-aconitane-4-(2-acetylamino)benzoate) acetyl-10-deoxysepaconitine Giant Typhonium Rhizome Lappaconitine, 98%, from Aconitum sinomontanum Nakai Lappaconitine ((+)-Lappaconitine) Aconitane-4,8,9-triol, 20-ethyl-1,14,16-trimethoxy-, 4-[2-(acetylamino)benzoate], (1α,14α,16β)- (+)-Lappaconitine (+)-Lappaconitine >90% Aconitum Sinomontanum Nakai Extract (+)-Lappacontine C32H44N2O8 (1a,14a,16b)-20-Ethyl-1,14,16-trimethoxyaconitane-4,8,9-triol 4-(2-acetylamino)benzoate) 20-Ethyl-1α,14α,16β-trimethoxyaconitane 4,8,9-triol 4-[2-(acetylamino)benzoate] 32854-75-4 C32H44N2O8 Inhibitors chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract