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99% Armodafinil raw powder supplier CAS 112111-43-0 AASraw Nootropics powder high purity buy Armodafinil powder samrt drugs

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ǀ. Raw Armodafinil powder basic Characters:

Name: Armodafinil

CAS: 112111-43-0

Molecular Formula: C15H15NO2S

Molecular Weight: 273.354

Melt Point: 156-158°C

Storage Temp: RT

Color: White to off white crystal powder

II. Armodafinil usage

1. Names:

Acronite、Armoda 、Armod 、Artvigil 、Nuvigil 、R-Modawake、 Waklert、Armodafinil powder (CAS 112111-43-0) 、

2. Raw Armodafinil powder Usage:

Armodafinil was oral used. In the market, there are usually the specification of 50mg、150mg、200mg、250mg .For mormal people,it should be run at 150-250mcg a day。

3. Warning on Raw Armodafinil powder

You are not allowed to take this If you have following symptom:

you are allergic to any ingredient in Armodafinil powder (CAS 112111-43-0) or to modafinil .

you have a history of developing a rash after taking armodafinil or modafinil.

you have a history of certain heart or heart valve problems (eg, mitral valve prolapse, left ventricular hypertrophy)

And if you have following Severe allergic reactions,please find doctor right away.

(rash; hives; itching; difficulty swallowing or breathing; tightness in the chest; swelling of the mouth, face, lips, throat, or tongue; unusual hoarseness); chest pain; fast or irregular heartbeat; fever, chills, or sore throat; mental, mood, or behavior changes (eg, aggression, agitation, anxiety, depression, exaggerated sense of well-being, hallucinations, irritability, nervousness); muscle or joint pain; shortness of breath; suicidal thoughts or actions; swelling of the legs; symptoms of liver problems (eg, dark urine, pale stools, persistent loss of appetite, right-sided stomach pain, yellowing of the skin or eyes); unusual bruising or bleeding; vomiting; weakness.

4.Further instructions:

Armodafinil has not been studied in pediatric patients in any setting and is not approved for use in pediatric patients for any indication.

In clinical trials of modafinil, the incidence of rash resulting in discontinuation was approximately 0.8% (13 per 1,585) in pediatric patients (age


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