(+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE

(+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE Struktur
42542-10-9
CAS-Nr.
42542-10-9
Englisch Name:
(+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE
Synonyma:
Methylenedioxymethamphetamine;XTC;3,4-MDMA;C07577;ecstacy;DL-MDMA;(+/-)-MDMA;AURORA KA-7748;(±)-MDMA solution;3,4-METHYLENDIOXYMETHAMPHETAMIN
CBNumber:
CB4221584
Summenformel:
C11H15NO2
Molgewicht:
193.25
MOL-Datei:
42542-10-9.mol

(+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE Eigenschaften

Siedepunkt:
bp0.4 100-110°
Dichte
1.100±0.06 g/cm3(Predicted)
Flammpunkt:
9℃
storage temp. 
2-8°C
pka
10.32±0.10(Predicted)
InChIKey
SHXWCVYOXRDMCX-UHFFFAOYSA-N
EPA chemische Informationen
1,3-Benzodioxole-5-ethanamine, N,.alpha.-dimethyl- (42542-10-9)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher F,T
R-Sätze: 11-23/24/25-39/23/24/25
S-Sätze: 7-16-36/37-45
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  1
Giftige Stoffe Daten 42542-10-9(Hazardous Substances Data)
Toxizität A novel psychoactive drug chemically related to the hallucinogenic agent MDA, but reported to be non-hallucinogenic. Obtained by direct synthesis, at high doses it is reported to show a stimulant-like effect in animals. Its LD50 is 97 mg/kg, i. p., 49 mg/kg, i.p., 14 mg/kg, i.v., and 22 mg/kg, i.v. in mice, rats, dogs, and monkeys, respectively. At higher doses, MDMA has pressor effects and produces tachycardia, and causes damage to serotonin neurons in both rats and monkeys. The (S)- (1)-enantiomer is more active than the (R)-(?′)-enantiomer and, like amphetamine, the pharmacological effects may be due to a release of endogenous monoamine neurotransmitter, probably serotonin and/or norepinephrine. MDMA is also an inhibitor of monoamine uptake into brain synaptosomes. Symptoms include pronounced mydriasis, with nystagmus and jaw clenching, and nausea also is often reported. This substance produces a feeling of well-being and euphoria and is similar in some respects to MDA, in that it seems to enhance a sense of empathy and emotional openness in users. Toxic reactions would appear to occur as a result of the pressor action, and sympathomimetic effects of the drug. No appropriate therapeutic intervention has been reported. Peripheral adrenergic blocking agents, or chlorpromazine, have been used, however, to prevent death in dogs following a lethal i.v. dose of the chemically related agent MDA.
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H225 Flüssigkeit und Dampf leicht entzündbar. Entzündbare Flüssigkeiten Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS02.jpg" width="20" height="20" /> P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H370 Schädigt die Organe. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P260, P264, P270, P307+P311, P321,P405, P501
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P260 Dampf/Aerosol/Nebel nicht einatmen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P311 GIFTINFORMATIONSZENTRUM/Arzt anrufen.

(+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE Chemische Eigenschaften,Einsatz,Produktion Methoden

Definition

ChEBI: A member of the class of benzodioxoles that is 1,3-benzodioxole substituted by a 2-(methylamino)propyl group at position 5.

Stoffwechselwegen

Four biotransformation pathways of 3,4- (methylenedioxy)methamphetamine (MDMA) in rats are identified as N-demethylation, O-dealkylation, deamination, and conjugation (O-methylation, O- glucuronidation, and/or sulfation). Specific MDMA metabolites identified are 3-hydroxy-4- methoxymethamphetamine, 4-hydroxy-3- methoxymethamphetamine, 3,4- dihydroxymethamphetamine, 4-hydroxy-3- methoxyamphetamine, 3,4- (methylenedioxy)amphetamine (MDA), (4-hydroxy-3- methoxyphenyl)acetone, [3,4- (methylenedioxy)phenyl]acetone, and (3,4- dihydroxyphenyl)acetone. MDMA is metabolized by 10 000 g rat liver supernatant to 4-hydroxy-3- methoxymethamphetamine, 3,4- dihydroxymethamphetamine, MDA, and [3,4- (methylenedioxy)phenyl]acetone. Also, the 10 000 g rat brain supernatant metabolizes MDMA to 4-hydroxy- 3-methoxymethamphetamine, 3,4- dihydroxymethamphetamine, 4-hydroxy-3- methoxyamphetamine, and MDA.

(+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

42542-10-9()Verwandte Suche:


  • 3,4-METHYLENDIOXYMETHAMPHETAMIN
  • N-Methyl-3,4-methylenedioxyamphetamine
  • 3,4-METHYLENDIOXYMETHAMPHETAMIN, >99% (HPLC)
  • N,1-Dimethyl-2-(1,3-benzodioxole-5-yl)ethanamine
  • N,α-Dimethyl-1,3-benzodioxole-5-ethanamine
  • N-Methyl methyldimethoxymethylamphetamine
  • N-Methyl-1-(1,3-benzodioxole-5-yl)-2-propanamine
  • N-Methyl-α-methyl-3,4-(methylenebisoxy)phenethylamine
  • ecstacy
  • C07577
  • Methanol (test (±)-MDMA, 1.0 mg/Ml)
  • (±)-MDMA solution
  • (+/-)-MDMA
  • DL-MDMA
  • AURORA KA-7748
  • (+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE
  • (±)-MDMA [(±)-3,4-Methylenedioxymethamphetamine]
  • (+/-)-3,4-MethylenedioxyMethaMphetaMin
  • 1-(1,3-Benzodioxol-5-yl)-N-methyl-2-propanamine
  • 1,3-Benzodioxole-5-ethanamine, N,alpha-dimethyl-
  • 3,4-Methylenedioxymethylamphetamine
  • 3,4-Methylenedioxymethylamphetamine, N-methyl-
  • Methamphetamine, 3,4-methylenedioxy
  • Methylenedioxymethamphetamine (MDMA)
  • 1-benzo[1,3]dioxol-5-yl-N-methyl-propan-2-amine hcl.
  • 1-(1,3-benzodioxol-5-yl)-N-methylpropan-2-amine
  • 1,3-Benzodioxole-5-ethanamine, N,α-dimethyl-
  • (+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE
  • 3,4-MDMA
  • Methylenedioxymethamphetamine
  • XTC
  • 42542-10-9
  • 54949-52-0
  • 42542-10-9 MDMA
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