ergotamine
- CAS No.
- 113-15-5
- Chemical Name:
- ergotamine
- Synonyms
- ergotamin;NSC 95090;ergotamine;Ergotamine (8CI);ergotamine USP/EP/BP;XCGSFFUVFURLIX-VFGNJEKYSA-N;12'-Hydroxy-2'-methyl-5'α-benzylergotaman-3',6',18-trione;12’-hydroxy-2’-methyl-5’alpha-(phenylmethyl)ergotaman-3’,6’,18-trione;6’,18-trione,12’-hydroxy-2’-methyl-5’-(phenylmethyl)-ergotaman-3(5’-alph;18-trione,12’-hydroxy-2’-methyl-5’-(phenylmethyl)-6(5’alpha)-ergotaman-3
- CBNumber:
- CB2865180
- Molecular Formula:
- C33H35N5O5
- Molecular Weight:
- 581.66
- MOL File:
- 113-15-5.mol
- Modify Date:
- 2024/8/28 13:53:22
Melting point | 241-249℃ |
---|---|
alpha | D20 -160° (chloroform) |
Boiling point | 651.33°C (rough estimate) |
Density | 1.0998 (rough estimate) |
refractive index | 1.7500 (estimate) |
pka | pKa 6.40±0.09(H2O t=24.0) (Uncertain) |
optical activity | -16020 (CHCl3) |
CAS DataBase Reference | 113-15-5 |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS06 |
---|---|
Signal word | Danger |
Hazard statements | H330-H311-H361-H301 |
Precautionary statements | P280-P302+P352-P312-P322-P361-P363-P405-P501-P201-P202-P281-P308+P313-P405-P501-P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501 |
RIDADR | 1544 |
HazardClass | 6.1(b) |
PackingGroup | III |
Toxicity | LD50 in mice, rats, rabbits (mg/kg): 62, 80, 3 i.v.; in cats: 11 s.c. (Rothlin) |
ergotamine Chemical Properties,Uses,Production
Uses
Analgesic (specific in migraine).
Uses
Ergotamine, 3′,6′,18′-trione,12′-hydroxy-2′-methyl-5′-benzyl-(5α)-ergotamine (12.2.14), is obtained via microbiological synthesis [52].As an α-adrenoblocker, ergotamine exhibits a direct vasoconstricting effect for which it is used in medicine, particularly for alleviation of severe migraine attacks. It is categorically counterproductive in chronic diseases because of the possibility of side effects such as triggering gangrene.
Definition
ChEBI: A peptide ergot alkaloid that is dihydroergotamine in which a double bond replaces the single bond between positions 9 and 10.
Purification Methods
Crystallise it from *benzene, then dry it by prolonged heating in high vacuum. It is very hygroscopic. [Beilstein 25 III/IV 964.]
ergotamine Preparation Products And Raw materials
113-15-5(ergotamine)Related Search:
Ergotamine tartrate (7CI),Ergotamine, tartrate (2:1) (salt) (8CI),Medihaler-ergotamine,ERGOTAMINE D-TARTRATE, PH EUR,ERGOTAMINE TARTRATE
DIHYDROERGOTAMINE
DIHYDROERGOTAMINE MESYLATE
ERGOCRISTINE
ergotamine
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12’-hydroxy-2’-methyl-5’alpha-(phenylmethyl)ergotaman-3’,6’,18-trione
18-trione,12’-hydroxy-2’-methyl-5’-(phenylmethyl)-6(5’alpha)-ergotaman-3
6’,18-trione,12’-hydroxy-2’-methyl-5’-(phenylmethyl)-ergotaman-3(5’-alph
ergotamine
Ergotaman-3',6',18-trione, 12'-hydroxy-2'-methyl-5'-(phenylmethyl)-, (5'α)-
Ergotamine (8CI)
NSC 95090
12'-Hydroxy-2'-methyl-5'α-benzylergotaman-3',6',18-trione
(5'alpha)-12'-Hydroxy-2'-methyl-5'-(phenylmethyl)ergotaman-3',6',18-trione
XCGSFFUVFURLIX-VFGNJEKYSA-N
Ergotaman-3',6',18-trione,12'-hydroxy-2'-methyl-5'-(phenylmethyl)-, (5'a)-
ergotamine USP/EP/BP
ergotamin
(6aR,9R)-N-[(2R,5S,10aS,10bS)-5-benzyl-10b-hydroxy-2-methyl-3,6-dioxooctahydro-8H-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl]-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide (ergotamine),
113-15-5
Organics