Recent content by essentials

have just recieved 100g of turanabol i herd a couple years back its quite a bitter compound to taste however im tasting a bit and cant taste much, tad of bitterness powder is similar to winstrol just not as fine.. id say similar appearance to dianabol minus the bitterness factor anyone...

any other ways to do this??

npp is not a long ester is short for nandrolone phenylpropionate are you saying youve made deca at 2%BA no BB? or Made NPP at 250mg %2BA no BB?

250mg npp !! any pip from that bro

have just recieved the powder was goin to do npp at the normall 100mg /ml using 2/20 now before i attempt i have no eo but isit possible to get npp at 200mg/ml with say a combo of 2%ba, 25%BB guys recipes much appreciated

or if to do the other way what size pin would you use to draw from the receive with through the septa without rubber flaking? 21g? although i dont want to be sitting there for ages trying to draw through a small guage

i do however have a crimper, caps rubbers ect and unsealed vials just neve thought of using them are you saying sterilize the vials , and withdraw 10ml from the lower receiver with a syringe and shoot straight into vial then seal? surely particles of air ect will come into contact?

ive just completed an eq 500 3%BA 20%BB just to be sure 4th jab now..painless even in delt

have a big question: what is the procedure for transfering the filtered gear from a filter unit into a sterile vial the way i have been doin this is by capping the lower receiver flask with a open top cap and silicon septa and drew up the oil through a 21g pin and shoot straight into vial with...

cottonseed oil

heres the image you can clearly see this residue still there even after 2-5 hours of it just sitting in this position with other ug vials i dont notice the slightest http://img704.imageshack.us/img704/8347/dsc00759r.jpg IMAGE OF VIAL ABOVE PLEASE HELP GUYS ALTHOUGH ITS FOR MYSELF I...

not it hasnt crashed made a batch of test eth 200 20%BB, 3%BA il take a pic and upload

forgot to say filtered using .22 millipore filter unit with septa rubber cap to allow drawing fluid into syringe then transferring into sterile vial

just created a batch of 200ml of tren eth im using sterile vials ect inserting a 22-25g while injecting the liquid into vial to relieve pressure although the vial is not full ( approx vial holds 14ml est ), as i shake the liquid around the vial it leaves like a residue that doesnt go no...

so if placing the finished vial into autoclave crimped and capped would cause a explosion? would dry heat be more effective? could you please talk me through a step by step guide when having access to autoclave