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Whaat is DMAA?
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2024-10-05 at 12:03 AM UTCIs it stimulant, will it kill me, what is it? I heard about it somewhere
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2024-10-05 at 12:08 AM UTCmild stimulant that used to be popular in preworkouts, a little stronger than caffeine
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2024-10-05 at 12:12 AM UTCYes it's a stimulant, It can kill you but probably won't. It's a chemical similar in structure to methamphetamines marketed as a weight loss/energy supplement and I'm pretty sure it's banned in the US.
You don't want to mess with stims crisp. Opiates are probably more your speed as they just make you sleepy and hungry which is probably what you need. -
2024-10-05 at 12:16 AM UTCI aint messin with it. Fucks with your heart and my heart cant handle more than being alive
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2024-10-05 at 2:48 AM UTC
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2024-10-05 at 3:03 AM UTCProve it
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2024-10-05 at 3:16 AM UTCDrugs are bad look around
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2024-10-05 at 3:16 AM UTCShit will make you retarded like me
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2024-10-05 at 3:44 AM UTCI dont do drugs 😇
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2024-10-05 at 4:08 AM UTC
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2024-10-05 at 4:43 AM UTCNo
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2024-10-05 at 4:47 AM UTCyes
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2024-10-05 at 7:36 AM UTCMethylhexanamine is synthesized by reacting 4-methylhexan-2-one with hydroxylamine, which converts the 4-methylhexan-2-one to 4-methylhexan-2-one oxime, which is reduced via catalytic hydrogenation; the resulting methylhexanamine can be purified by distillation.[17]: 995–996
4-methylhexan-2-one - also known as methyl isoamyl ketone, is a ketone often used as a solvent in various industrial processes. It's typically produced by a Friedel-Crafts acylation reaction, where isoamyl alcohol reacts with acetyl chloride or acetic anhydride in the presence of a catalyst like aluminum chloride.
Starting materials: You need isoamyl alcohol (3-methylbutanol) and an acetyl group source (such as acetyl chloride or acetic anhydride).
Reaction: The acetyl group is added to the isoamyl alcohol in the presence of a strong catalyst (like aluminum chloride or sulfuric acid).
Product: This gives you 4-methylhexan-2-one.
Isoamyl alcohol can be synthesized by condensation of isobutene and formaldehyde which produces isoprenol, then hydrogenation. It is a colourless liquid of density 0.8247 g/cm3 (0 °C), boiling at 131.6 °C, slightly soluble in water, and easily dissolved in organic solvents. It has a characteristic strong smell and a sharp burning taste.
https://en.wikipedia.org/wiki/Isobutylene
R-600a
2.4. Unknown Acute Toxicity (GHS-US)
No data available
3.1. Substance
Name Product Identifier % Classification (GHS-US,CA)
Isobutane* (CAS No) 75-28-5 100 Simple Asphy
Flam. Gas 1, H220
Liquefied gas, H280
https://redtek.ca/wp-content/uploads/2020/07/SDS_600a.pdf -
2024-10-05 at 7:45 AM UTCTldr
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2024-10-05 at 8:08 AM UTCI lost shit loads when I was taking phenibut a couple of years ago, I also lost my sanity and it took awhile to get it back.
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2024-10-05 at 8:16 AM UTCI dont think you ever got it back, but good job for thinking you did
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2024-10-05 at 1:47 PM UTCI ate a turtle egg and the turtle didn't appreciate it.
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2024-10-05 at 5:27 PM UTC
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2024-10-05 at 5:31 PM UTC
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2024-10-05 at 5:47 PM UTC
Originally posted by the man who put it in my hood
Originally posted by the man who put it in my hood chemistry is so cool
Pears soap was made using a process entirely different from that for other soaps. A mixture of tallow and other fats was saponified by an alkali. Clearly, this is currently caustic soda (sodium hydroxide), since the ingredients list shows sodium salts of fatty acids, but a chemist reports that in the 1960s, caustic potash (potassium hydroxide) was used. It has not been possible to determine what was used in the early days of the product, as the writings of Francis Pears mention only alkali in industrial methylated spirits. After saponification was completed, the resulting glycerol was left in the batch. Batches were made not in huge pans, but in small kettle-like vessels. As soon as the translucent amber liquid had cooled enough to solidify, it was extruded into opaque oval bars that were cut into bath- or toilet-weight tablets, ready for beginning their long spell in the drying rooms (ovens). The hot liquid soap fresh from the vessel had a total fatty matter (TFM) of 45% compared with the TFMs of 70–80% usual in soaps made by the conventional method. The TFM increased considerably as the alcohol content fell during drying. The concave shape of the soap is formed by shrinkage while the soap is drying, and is not due to deliberate moulding.