Prometheuz
(Stranger) 04-04-03 09:47 No 423824 |
DOB solubility | Bookmark | ||||||
If some deranged person was to make a 1 mg/ml solution of DOB-HCl, would 50% ethanol be a suitable choice? Would another dilutant be preferred? Also, does anybody have an educated guess at DOB-HCl's solubility in DMSO? Would freebase DOB be more soluble? I can't seem to find the solubility-data myself, so I would appreciate any help. To fathom Hell or soar angelic Just take a pinch of psychedelic |
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Bandil (Hive Bee) 04-04-03 10:54 No 423828 |
Check this out ;) | Bookmark | ||||||
Check this out ;) http://esc.syrres.com/interkow/webprop.e if the solubility is 1100 mg/L for the freebase(as i suppose this is), then the HCl would definately be soluble enough! CAS Number : 032156-26-6 Chem Name : 2,-5-DIMETHOXY-4-BR AMPHETAMINE Mol Formula: C11H16BrNO2 Mol Weight : 274.16 Melting Pt : Boiling Pt : Water Solubility: Value : 1100 mg/L Temp : 25 deg C Type : EST Ref : MEYLAN,WM ET AL. (1996)Log P (octanol-water): Value : 2.58 Type : EXP Ref : HANSCH,C & LEO,AJ (1985) Vapor Pressure: Value : 0.000116 mm Hg Temp : 25 deg C Type : EST Ref : NEELY,WB & BLAU,GE (1985)pKa Dissociation Constant: Value : Temp : Type : Ref : Henry's Law Constant: Value : 1.5E-009 atm-m3/mole Temp : 25 deg C Type : EST Ref : MEYLAN,WM & HOWARD,PH (1991)Atmospheric OH Rate Constant: Value : 6.04E-011 cm3/molecule-sec Temp : 25 deg C Type : EST Ref : MEYLAN,WM & HOWARD,PH (1993) Cops are not there to help you, they're there to bust you. |
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terbium (Old P2P Cook) 04-04-03 19:13 No 423898 |
Vodka as a preservative. | Bookmark | ||||||
I think that 50% ethanol would be a good choice as it would prevent any microbes from growing that might consume the DOB. All those moments will be lost in time, like tears in rain. |
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Rhodium (Chief Bee) 04-04-03 19:43 No 423901 |
What is the nutritional value of DOB? | Bookmark | ||||||
I wonder if there is any G-protein coupled receptors in such critters which would correspond to the 5-HT2 receptors in mammals? Or are such things restricted to vertebrates only? In any way, it is easy to smile at the thought of something eating its own weight in DOB... |
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catastrophe (Hive Bee) 04-06-03 01:36 No 424181 |
Solubility | Bookmark | ||||||
Since someone brought up the issue of solubility, can anyone suggest a procedure to seperate 2,5-DMA from DOB(I)? The synthesis of DOI where silver sulphate is reacted with iodine in EtOH will leave behind some 2,5-DMA, is there anyway to seperate it without column chromatography? ../rhodium /doisynt
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yellium (I'm Yust a Typo) 04-06-03 01:48 No 424186 |
Say that you have 80% yield. | Bookmark | ||||||
Say that you have 80% yield. That would give you 0.8 mg DOB and 0.2 mg 2,5-DMA in a mg. Do you think you could feel the effects of about 0.5 mg 2,5-DMA on top of the DOB? |
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Rhodium (Chief Bee) 04-06-03 01:59 No 424190 |
I would feel it in my obsessive quality ... | Bookmark | ||||||
I would feel it in my obsessive quality control center in my brain |
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yellium (I'm Yust a Typo) 04-06-03 02:06 No 424193 |
I knew you would say that :-) | Bookmark | ||||||
I knew you would say that :-) |
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chemotype (Stranger) 04-06-03 09:54 No 424275 |
You won't be able to differentiate the ... | Bookmark | ||||||
You won't be able to differentiate the effects. 2,5-DMA's activity is over 100 mg. I agree with Rhod but running a column of a primary amine sucks. BOC it and it and it makes it streak a lot less or add AcOH or DIEA to the eluent. DOB, such pleasures... but such horrifying pains... |
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Rhodium (Chief Bee) 04-07-03 00:02 No 424392 |
TLC Rf Values for DOB, DMA, Meth & Amphetamine (Rated as: excellent) |
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You don't need to run a column on the freebase as long as the DOB is present in a significant excess over any unreacted 2,5-DMA. Just recrystallize the final amine salt once or maybe twice (TLC will tell if you have gotten rid of the starting material). The recrystallization solvent is then evaporated, A/B'ed and the recovered 2,5-DMA (obviously contaminated with DOB) is then subjected to another bromination to increase the total yield (this is only necessary if you are working with a significant amount of amine, if you just brominated a couple of millimoles in the first place, re-bromination is futile). TLC Values DOB:1 Eastman Chromogram 6060 fluorescent gel sheet; Rf 0.38 (CHCl3/MeOH 8:1), Rf 0.22 (EtOAc/C6H12/NH4OH/MeOH/H2O 70:15:2:8:0.5) DMA:2 References [1] J. Ass. Off. Anal. Chem. (JAOAC) 59(5) 1162-1169 (1976) [2] J. Ass. Off. Anal. Chem. (JAOAC) 57(1) 70-78 (1974) |
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catastrophe (Hive Bee) 04-10-03 20:48 No 425439 |
Thanks for the Rfs | Bookmark | ||||||
Thanks Rhodium, that was an excellent response, thanks for the Rfs too. A FOAF says the iodination procedure detailed on your page is a good procedure for 2,5-DMA, but it is best done under red-light or in the dark. Yellium, if somebody is taking 3mg of a compound, how comfortable is it to know that maybe 20% of it is something else (although inactive)? If someone wants to take a 3mg dose, they take 3,5mg instead to compensate for impurities? YUCK!! Sorry, but SWIM doesn't understand how bees go so far to make their compounds, then settle for impurties in the final product. |
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hest (Hive Adickt) 04-10-03 22:30 No 425470 |
Īmpure | Bookmark | ||||||
With DOB it's not a big problem, eating 0,5mg shit is usual ok. Try with mescaline, then 20% is 100mg. Eating 100mg is not alwayes good. |
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