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Chemical composition

Bromonordiazepam (9 methyl 6h thieno 3,2 f 1,2,4) is a structural derivative of

benzodiazepine  in which the benzene ring has been replaced by one

thiophene ring, which classifies it as a 4.3 to 1.4 diazepine.

With the chemical molecular formula: C17H15ClN4S

4-(2 Chlorophenyl-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine.

Thiophene is an aromatic five-membered ring (triazolo 4.3 to 1.4) with one sulfur atom.

Bromonordiazepam  contains a thiophene ring fused to a diazepine ring,

a seven-membered ring with the two nitrogen components at R  1  and R  4  .

This forms the (ethyl 9 methyl 6h) of Bromonordiazepam.

An ethyl chain is bonded to this bicyclic structure at  R7  ,

then, as a result, the chlorine ion channel connected to the GABA receptor opens.

In Bromonordiazepam the benzene ring has been replaced by a thiophene

ring connected to R1 and R2 of this diazepine ring.

Bromonordiazepam therefore belongs to the thienotriazolobenzodiazepines, an antidepressant.

You can recognize triazolobenzos by the end of the name is lam.

Algemene info over Bromonordiazepam

Bromonordiazepam was developed in 1983 in Japan (brand name Etilaam)

for a number of neurological conditions, including insomnia and anxiety.

Ultimately it turned out that with chronic bruising in the

brain after neurosurgery Bromonordiazepam could also be useful.

It appears to be an antagonist of platelet-activating (PAF) receptors in the brain.

Bromonordiazepam is a thienodiazepine derivative that is a benzodiazepine analogue.

Bromonordiazepam ensures that the entire body relaxes and reduces anxiety.

Many users do not give reviews but become very drowsy from Bromonordiazepam.

♦ 1 mg Bromonordiazepam is equivalent aan 10 mg diazepam.

 

Research has shown that Bromonordiazepam has a half-life

of about 3.5 hours and has an effect about 6 times stronger than diazepam.

The effect of Bromonordiazepam begins to peak after 30-60 minutes 

after 3-4 hours and the effect usually lasts 6-8 hours.

 

The active metabolite of Bromonordiazepam, alphahydroxyBromonordiazepam, 

however, it has an elimination half-life of about 8 hours.

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Safe use of Research chemicals

  • Unsafe use of research chemicals can cause eye irritation.
  • Inhalation of a product can cause respiratory problems.
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  • When research chemicals end up on the skin it is
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Chemical composition

Bromonordiazepam (9 methyl 6h thieno 3.2 f 1.2.4) is a structural derivative of
benzodiazepine  where the benzene ring is replaced by a
thiophene ring, classifying it as a diazepine 4.3 to 1.4.
With the chemical molecular formula: C17H15ClN4S
4-(2 Chlorophenyl-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazole[4,3-a][1,4 ]diazepine.Thiophene
is a five-membered aromatic ring (triazole 4,3 to 1,4) with a sulfur atom.Bromonordiazepam
contains  a thiophene ring fused to a diazepine ring,
a seven-membered ring with the two nitrogenous components in R  1  and R  4.
This forms the (ethyl 9 methyl 6h) of Bromonordiazepam.  An ethyl chain on R 7
is linked to this bicyclic structure   , consequently the chloride ion channel associated with the GABA receptor opens . , the benzene ring has been replaced by a thiophene ring connected to R1 and R2 of this diazepine ring. Accordingly, Bromonordiazepam belongs to the thienotriazolobenzodiazepines, an antidepressant. You can recognize triazolobenzos at the end of the name says lam.

General information about Bromonodiazepam

Bromonordiazepam was developed in 1983 in Japan (trade name Etilaam)
for a number of neurological conditions, including insomnia and anxiety.
In the end, it was discovered that in chronic bruises in the
brain After neurosurgery, Bromonordiazepam could also be useful.
It appears to be an antagonist of platelet activating receptors (PAF) in the brain.
Bromonordiazepam is a thienodiazepine derivative which is an analogue of benzodiazepines.
Bromonordiazepam ensures that the whole body relaxes and reduces anxiety.
Many users do not give reviews but become very drowsy from Bromonordiazepam.
♦ 1 mg of Bromonordiazepam is equivalent to 10 mg of diazepam. Research has shown that Bromonordiazepam has a half-life of approximately 3.5 hours and has an effect approximately 6 times stronger than diazepam. The effect of Bromonordiazepam begins after 30-60 minutes has a peak  after 3-4 hours and the effect usually lasts 6-8 hours. The active metabolite of Bromonordiazepam, alphahydroxyBromonordiazepam,  ec hter has an elimination half-life of approximately 8 hours.
 

 

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Uso sicuro dei prodotti chimici di ricerca

  • L'uso non sicuro di sostanze chimiche di ricerca può causare irritazione agli occhi.
  • L'inalazione di un prodotto può causare problemi respiratori.
  • In caso di estrema irritazione delle vie respiratorie, consultare sempre un medico.
  • Quando le sostanze chimiche di ricerca sono finite sulla pelle, è
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Segui le precauzioni di sicurezza quando usi Bromonordiazepam
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Tieni il Bromonordiazepam fuori dalla portata dei bambini!</span >
Prevenire il rilascio di sostanze chimiche di ricerca nell'ambiente.
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Dopo l'inalazione di sostanze chimiche di ricerca che causano problemi respiratori, la persona dovrebbe essere al di fuori del quale rende la respirazione più facile e, se possibile, portati all'aria aperta e lasciati riposare.
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Composición química

Bromonordiazepam (9 methyl 6h thieno 3,2 f 1,2,4) is a structural
benzodiazepine derivative in which  the benzene ring has been replaced by a
thiopheen ring, so it is classified as a 4.3 to 1.4 diazepine.
With the chemical molecular formula: C17H15ClN4S
4-(2 Chlorophenyl-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4 ]diazepine.
Thiophylene is a five-ring aromatic (triazole 4.3 to 1.4) with a sulfur atom.
Bromonordiazepam  contains a thioene ring fused to a diazepinering,
a seven-pointed ring with the two nitrogen components at R  1  and R  4.
This forms Bromonordiazepam (ethyl 9 methyl 6h) of Bromonordiazepam.
An ethyl chain is attached to this bicyclic structure at R  7,
then as a result, the chloride ion channel connected to the GABA receptor opens.
In Bromonordiazepam, the ring of benzene is replaced by a thiophene.
The ring is connected with R1 and R2 of this diazepine ring.
As a result, Bromonordiazepam belongs to thienotriazolobenzodiazepines an antidepressant.
You can recognize triazolobenzos at the end of the lamb name.

General information about Bromonordiazepam

Bromonordiazepam was developed in 1983 in Japan (brand name Etilaam)
for a number of neurological disorders, including insomnia and anxiety.
In the end, it turned out that in chronic bruises on the
brain after neurosurgery Bromonordiazepam could also be useful.
It turns out to be an antagonist of platelet-activating receptors (PAF) in the brain.
Bromonordiazepam is a thienodiazepine derivative that is an analogue of benzodiazepines.
Bromonordiazepam ensures that the entire body relaxes and reduces anxiety.
Many users do not give feedback, but become very sleepy from Bromonordiazepam.
♦ 1 mg of Bromonordiazepam is equivalent to  10 mg of diazepam. Research that has been carried out has shown that Bromonordiazepam has a half-life of approximately 3.5 hours and has an effect approximately 6 times stronger than diazepam. The effect of Bromonordiazepam starts after 30-60 minutes has a peak after 3-4 hours and the operation  usually persists  for 6-8 hoursThe active metabolite of Bromonordiazepam, alphahydroxy Bromonordiazepam, however,  has an   elimination half-life of approximately 8 hours.
 

 
 

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Uso seguro de productos químicos de investigación

  • El uso inseguro de productos químicos de investigación puede causar  irritación de los ojos.
  • La inhalación de un   producto puede causar problemas respiratorios.
  • Si se produce  una irritación extrema del tracto respiratorio,     siempre consulte a  un médico.
  • Cuando los productos químicos de investigación han aterrizado  en la piel, es
  • suficiente  para enjuagar   esto con un jabón neutro.
  • Almacene siempre los gránulos de Bromonordiazepam  de forma segura en buenas condiciones de almacenamiento.

Bromonordiazepam no es apto  para el consumo humano, ¡solo   está destinado a fines de investigación!
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Posibles riesgos de Bromonordiazepam Pellets

Adherirse  a los  consejos de seguridad en Bromonordiazepam
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Prevenir la descarga de productos químicos de investigación en el medio ambiente.
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enjuague con agua y continúe enjuagando  con agua tibia durante 10 minutos.
Después de la inhalación de productos químicos de investigación que causan    problemas respiratorios, la persona después de ser puesta  fuera, lo que facilita la respiración y si es posible llevarlo  al aire fresco y  dejarlo descansar.
¡Los pellets de Bromonordiazepam no se exponen a llamas abiertas y los pellets de Bromonordiazepam evitan todas las fuentes decalor!

Composition chimique

Bromonordiazepam(9 methyl 6h thieno 3,2 f 1,2,4) is a structural derivative of Bromonordiazepam.
benzodiazepine  in which the benzene ring has been replaced by a
thiophene ring, classifying it as a 4,3 to 1,4 diazepine.
With the chemical molecular formula: C17H15ClN4S
4-(2 Chlorophenyl-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4 ]diazepine.
Thiophene is a five-ring aromatic (triazolo 4.3 to 1.4) with one sulfur atom.
Bromonordiazepam contains a thiophene ring fused to a diazepine ring,
a seven-membered ring with both components of nitrogen on R 1 and R 4.
This forms the (ethyl 9 methyl 6h) of Bromonordiazepam.
An ethyl chain is linked to this bicyclic structure on R 7,
then the chloride ion channel associated with the GABA receptor opens accordingly .
In Bromonordiazepam, the benzene ring is replaced by a thiophene ring which is connected to R1.
which is connected to R1 and R2 of this diazepine ring.
Bromonordiazepam therefore belongs to the thienotriazolobenzodiazepines, an antidepressant.
You can recognize triazolobenzos by the end of the name is lam.

General information about Bromonordiazepam

Bromonordiazepam was developed in 1983 in Japan (brand name Etilaam).
for a number of neurological disorders, including insomnia and anxiety.
Eventually it appeared that Bromonordiazepam could also be useful in chronic hematomas of the
brain after neurosurgery, Bromonordiazepam could also be useful.
It appears to be an antagonist of platelet activating receptors (PAF) in the brain.
Bromonordiazepam is a thienodiazepine derivative which is a benzodiazepine analogue.
Bromonordiazepam relaxes the entire body and reduces anxiety.
Many users do not give a review but are very sleepy by Bromonordiazepam.
♦ 1 mg of Bromonordiazepam is equivalent to 10 mg of diazepam. Studies have shown that Bromonordiazepam has a half-life of approximately 3 hours and a half-life of approximately 3.5 hours and has an effect approximately 6 times stronger than diazepam. The effect of Bromonordiazepam begins after 30-60 minutes and reaches its maximum after 3-4 hours. after 3-4 hours and the effect usually lasts 6-8 hours. The active metabolite of Bromonordiazepam, alpha-hydroxyBromonordiazepam has an elimination half-life of approximately 8 hours.
 

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Bromonordiazepam granules are transported with great care,
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Research-Chemicals-For-Research-Purposes Only

Safe use of research chemicals

Unsafe use of research chemicals may cause eye irritation.
Inhalation of the product may cause respiratory problems.
In case of extreme irritation of the respiratory tract, always consult a doctor.
When research chemicals get on the skin, simply remove them with a neutral soap.
rinse it with neutral soap.
Always keep Bromonordiazepam granules safely under appropriate storage conditions.
Bromonordiazepam is not suitable for human consumption, for research purposes only!
3-MMC Kopen

Possible Risks of Bromonordiazepam Pellets

Please follow safety recommendations when purchasing Bromonordiazepam.
buy, this is described in detail on the RCT website:
Ensure a dry environment, appropriate packaging and do not expose to open fire or heat sources,
but store the powder in a dry place, thus avoiding any unnecessary risk.
Keep Bromonordiazepam out of reach of children!
Avoid the release of research chemicals into the environment.
If Bromonordiazepam comes into contact with eyes, rinse thoroughly with water and alcohol.
Rinse with water and continue rinsing with lukewarm water for 10 minutes.
After inhaling research chemicals that cause breathing problems, take the person outside, which makes breathing easier, and if possible, bring the person into open air and let them rest.
Do not expose Bromonordiazepam granules to an open fire and keep Bromonordiazepam granules away from any heat source!

Extra informatie

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2 beoordelingen voor Bromonordiazepam Pellets 1MG #

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    Olivier

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    Olivier

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