MESO-Rx Sponsor Pharmacom Labs officials and our Basicstero.com store

That’s odd. I absolutely feel it at 100mg preworkout of the test suspension oil, BUT I’m only on 200mg/week of testosterone. Are you on cycle and a high dose of testosterone already?
I'm on 105mg "TRT" currently. Ill have to take some one offs from Marek and dose up a couple hours prior… it could be my body. People say prop feels diff to but I didn’t notice anything with that either.
 
Just placed my first order of npp, excited to receive it and looking forward to doing more business in the future.
Nice. I think you'll like the products; Pharmacom Labs is some of the highest quality gear in the world.
Just be sure to run some Testosterone with the NPP because the NPP will shut down your natural testosterone production.
 
Love your products. Running your tren ace, test prop, Superdrol, tesos and halotestin. Any chance of you ever making igf1 or igf1 lr3?
Wow Tren-A + SDrol + Halo. That's pretty hardcore bro!
Awesome powerful compoundds, but be careful; don't run those harsh orals too long.

What's the experience like on the TESOS? Is it working?
How are you using it (how often)? what do you feel?

For guys that read along to learn about orals such as Superdrol and/or Halo,
here is a list of some liver support supplements to keep people as healthy as possible while running orals:
TUDCA, TAD600, NAC, SAMe, TMG, Choline, Himalaya Liver Care (Liv52), and European Milk Thistle (I like LEF brand).
I hope that helps some guys.
 
Nice. I think you'll like the products; Pharmacom Labs is some of the highest quality gear in the world.
Just be sure to run some Testosterone with the NPP because the NPP will shut down your natural testosterone production.

Thanks bro
I'm currently on prescribed test-c 100 2x week & HCG, might switch everything over to you if my npp order is successful.
 
Just placed my first order of npp, excited to receive it and looking forward to doing more business in the future
Order U1C744X7
Hi, we hope you'll be satisfied with the quality of our products, if you have any questions or need help in the future - feel free to email us right here, we'll always help.
 
Love your products. Running your tren ace, test prop, Superdrol, tesos and halotestin. Any chance of you ever making igf1 or igf1 lr3?
Hi, thank you for your review of our products.

There is no information about the release date of the new products yet, but we will be sure to post here as soon as the information is available.
 
Check out these informative posts to learn more about some of Pharmacom Labs innovative products!


The NEW Fat-Loss Product TESOS (Tesofensine):
TESOS – An Exciting NEW Fat-Loss Product from Pharmacom Labs! – is Now Available in the Basicstero Store.
Code:
https://basicstero.ws/fat-loss/tesos
This innovative Oral-Line Fat-Loss product is currently offered as a 50 count blister strip of 0.5 mg tablets (1 BLISTER, 50 PILLS).

Tesofensine Information:
Tesofensine is a unique new generation Triple Serotonin Norepinephrine Dopamine Reuptake Inhibitor (SNDRI).
SNDRI belong to the class of psychoactive antidepressants. They affect neurotransmitters in the brain, exactly serotonin, norepinephrine and dopamine. Tesofensin affects the brain qualitatively, helping a person to feel maximum saturation during eating, and reduce appetite significantly.
Tesofensin was originally developed and patented by NeuroSearch A/S (Denmark) to cure Parkinson's and Alzheimer's diseases.
acts centrally, suppress appetite, regulate the availability of dopamine receptors and stimulate α1-adrenergic receptors.
appetite decreases within 14 days, there is a higher level of satiety and less desire to eat.
increases significantly fat oxidation and reduces adipose tissue.
improves the level of insulin sensitivity, which leads to higher glucose metabolism.
alters the expression of dopaminergic receptors in the striatum of the brain, as well as their binding.
the energy consumption increases greatly within 14 days.
The drug has a long half-life, which is 8-9 days, and metabolized mainly in the liver by CYP3A4 to the disalkyl metabolite M1 (NS-2360), which is the only metabolite found in human blood plasma.


Chemical name: (1R,2R,3S,5S)-3-(3,4-dichlorophenyl)-2-(ethoxymethyl)-8-methyl-8-azabicyclo[3.2.1]octane
Formula: C17H23Cl2NO
Anabolic activity index: not a steroid
Androgenic activity index: not a steroid
ACTIVE HALF-LIFE: 9 days
CLASSIFICATION: psychoactive antidepressants.
DOSAGE: 0.25 mg -1 mg
ACNE: no
WATER RETENTION: no
HBR: Perhaps
HEPATOXITY: Low
AROMATIZATION: no

The Basicstero Team hopes this NEW Pharmacom Labs Fat-Loss product will help you reach your goals!


FARESTOS (Toremifene) a More Modern SERM:
Toremifene (Fareston) – A More Modern SERM – is Available in the Basicstero Store

Toremifene Citrate is a selective estrogen receptor modulator (SERM) derived from triphenylethylene. It was patented and approved in Europe in the mid 1990's to treat metastatic ER+ breast cancer in postmenopausal women. Toremifene (Fareston) is an analogue of Tamoxifen and Clomid which can be used to replace these older compounds.
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In bodybuilding toremifene citrate is used by men as a drug for post-cycle therapy (PCT) to counteract and/or block some of the effects of excessive estradiol in the body as a result of aromatization of various androgens used. In particular, toremifene is used to restore levels of endogenous testosterone in blood as well as to prevent the estrogen-related side effect of gynecomastia.
In its chemical structure toremifene is very similar to tamoxifen and clomiphene. However, toremifene is a new generation drug and has less toxic side effects than tamoxifen.

For a more effective boost in testosterone production toremifene dosage should be in the range of up to 120 mg per day. This dose can be maintained for a first week of PCT; then, 100mg/day for the second week of PCT; and, finally 60mg/day for the remaining 3 – 4 weeks of PCT. Of course, exact dosages should be determined individually based on blood work results.

This innovative SERM is currently available as a 50 count blister strip of 20 mg tablets at the link in the "code" box below:
Code:
https://basicstero.ws/pct/farestos-pills-20mg

Toremifene Information:
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Toremifene Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is an anti-estrogenic drug, specifically classified as a Selective Estrogen-Receptor Modulator (SERM) with mixed agonist and antagonist properties. It is a non-steroidal triphenylethylene derivative, similar in structure and action to both Nolvadex (tamoxifen citrate) and Clomid (clomiphene citrate). Toremifene citrate is used for the treatment of breast cancer in postmenopausal women with estrogen-receptor positive or estrogen-receptor unknown (unsure if the cancer is estrogen responsive) tumors. It works by attaching to the estrogen receptor in various tissues in a competitive manner, blocking endogenous estrogen from exerting biological activity. As an anti-estrogen in many tissues, male bodybuilders and athletes may use toremifene citrate to counter some of the side effects associated with the use of aromatizable or estrogenic anabolic/androgenic steroids. This may include gynecomastia, body fat gain, and increased water retention.

The triphenylethylene compounds (toremifene citrate, tamoxifen citrate, clomiphene citrate) tend to be somewhat intrinsically estrogenic in the liver. This means that while they can block estrogenic activity in some areas of the body, they can actually act as estrogens in this other key area. Estrogenic action in the liver is important in the regulation of serum cholesterol (it tends to support HDL synthesis and LDL reductions). Since steroid-using bodybuilders are already dealing with the negative cardiovascular effects of these drugs, compounding the issue with aromatase inhibitors (which will lower total serum estrogen levels) may not always be the best option. Using a drug that blocks gynecomastia, for example, while at the same time supporting improved cholesterol values, might be much more ideal. In terms of which triphenylethylene agent is most effective in this regard, evidence suggests that the positive lipid altering benefits of toremifene are significantly stronger than those of tamoxifen, a drug normally favored for this purpose. Toremifene citrate may, therefore, be the preferred antiestrogen among those concerned about their lipid profiles.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate was approved by the FDA as a prescription drug in 1997. It is sold in the U.S. under the Fareston brand name, which is made by GTx, Inc. Fareston is also available in over two dozen other countries including Australia, Austria, Belgium, Czech Republic, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Mexico, Netherlands, New Zealand, Portugal, Russia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and the United Kingdom.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is classified as a selective estrogen receptor modulator, with both agonist and antagonist properties. It has the chemical designation 2-{p-[(Z)-4-chloro-1,2-diphenyl-1-butenyl]phenoxy}-N,N-dimethylethylamine citrate (1:1).

Side Effects (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate appears to be well tolerated, with a low incidence of serious side effects. In clinical trials, common side effects associated with its use included hot flashes (35%), sweating (20%), elevated liver enzymes (19%), nausea (14%), vaginal discharge (13%), dizziness (95%), edema (5%), vomiting (4%), and vaginal bleeding (2%). Other observed rare adverse events that may or may not be linked to toremifene citrate administration include low white blood cell and platelet counts, skin discoloration or dermatitis, constipation, difficulty breathing, partial motor paralysis, tremor, vertigo, itching, anorexia, visual disturbances, loss of strength, hair loss, depression, jaundice, and rigors (stiffening of the muscles). Antiestrogens may harm the developing fetus and should never be used during pregnancy.

Administration (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is FDA approved for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors. The recommended dose is one 60 mg tablet administered once per day. When used (off-label) to mitigate the estrogenic side effects of anabolic/androgenic steroid use, male athletes and bodybuilders may use 30 mg to 60 mg per day during steroid treatment.

Availability (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is widely available under the Fareston brand name. It is not commonly sold on the black market, nor is it a high-profile item for counterfeiters.


Toremifene vs. Tamoxifen: Why Toremifene is a healthier SERM and less toxic than Tamoxifen:
Addendum: structural considerations and an explanation of toremifene’s decreased carcinogenicity.

Why is Tamoxifen Carcinogenic? What Makes Toremifene Less Toxic?
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Most of these compounds may lead to long-term toxic effects. For instance, tamoxifen induces liver cancer in rats after prolonged administration, which has been attributed to the generation of DNA-alkylating species from the metabolism of the stilbene framework. It has been proposed that cytochrome P450 hydroxylates tamoxifen at the allylic position of the ethyl side chain, leading to an alcohol, which can generate a highly delocalized allylic cation 3.6 and therefore alkylate DNA to give product 3.7 through an SN1 mechanism (Fig. 3.6 below).
(Reference: Triphenylethylene - an overview | ScienceDirect Topics)

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This proposal also explains the lack of carcinogenicity of toremifene, which can be attributed to destabilization of the positive charge in 3.8 by the inductive effect of the chlorine substituent at the position adjacent to the allylic carbon (Fig. 3.7 below).
(Reference: Triphenylethylene - an overview | ScienceDirect Topics)

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DROLOS (Superdrol):
DROLOS – The New SUPERDROL Product from Pharmacom Labs! – is Now Available in the Basicstero Store.

Methyldrostanolone is scientifically known as Superdrol and it is arguably the most effective and potent oral anabolic steroid to be utilized over the last decade. Superdol is very similar to Masteron, with the only difference being that Masteron though is lacking an ester chain. The name Superdrol is a combination of the words “super” and “anadrol." Superdrol is an awesome steroid for bulking, though some bodybuilders also use it as part of their cut as it yields very dry and hard gains with no bloating or water retention. It was created back in the 1950s by doctors who were looking to create a drug to destroy tumors. Sadly, this wasn’t achievable, but they did find that the oral steroid promoted huge increases in lean muscle mass and strength. However, Superdol wasn’t released until 2005.

The active steroidal hormone in Superdrol is Methyldrostanolone. It is a structurally altered form of Drostanolone, with an added methyl group at the 17th carbon position. There is also an added methyl group at the carbon 2 position. These changes ramp-up the anabolic potential of this drug, giving it an anabolic rating of 400.

Effects:
Increases muscle mass.
Improves recovery.
Improves athletic performance.

This Powerful Oral-Line product is currently offered as 10 mg tablets available at the link in the "code" box below:

Code:
https://basicstero.ws/oral-steroids/drolos

Superdrol Information:

Superdrol Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone, also known as methasteron, is a potent oral anabolic steroid that was never sold as a prescription drug. In structure, this steroid is a close derivative of drostanolone (Masteron). The only difference in this case is the addition of a c-17 alpha methyl group, a modification that gives this steroid high oral bioavailability. The two agents remain very comparable, however. Both methyldrostanolone and drostanolone are nonaromatizable, so there is no difference in the estrogenicity of these two steroids, and both steroids retain favorable anabolic to androgenic ratios. Lab assays do put Superdrol ahead here, however, showing it to possess 4 times the anabolic potency of oral methyltestosterone while displaying only 20% of the androgenicity (a 20:1 ratio, compared to 3:1 ). The exact real-world relevance of these figures remains to be seen, however. Methyldrostanolone is favored by athletes for its moderate anabolic properties, which are usually accompanied by fat loss and minimal androgenic side effects.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone was first described in 1959.1 This steroid was developed by the international pharmaceuticals giant Syntex, alongside such other wellknown anabolic agents as drostanolone propionate and oxymetholone. Unlike rostanolone and oxymetholone, however, this steroid (at least in its basic form) was never released as a medicinal product. It was only sold for a brief period of time as a modified hormone called dimethazine. Dimethazine is made from two molecules of methyldrostanolone that are bonded together, which are later metabolically separated to yield free methyldrostanolone. So while technically methyldrostanolone itself was never sold as a prescription agent, we can say that the drug was one utilized medicinally (for more information see the Roxilon drug profile). Otherwise, the methyldrostanolone molecule remained an obscure research steroid only, and was never itself approved for use in humans. Methyldrostanolone was released in early 2005 as an over the counter "grey market" anabolic steroid in the United States. The drug was being sold without restrictions as a nutritional supplement product, barring some minimum age disclaimers by the manufacturer. No State or Federal laws identify this drug as an anabolic steroid, which remove the legalities associated with being a Class Ill controlled substance like other steroids. This is simply due to the fact that methyldrostanolone was not in commerce at the time such laws were written, and was unknown to lawmakers. It was never legal to sell as a dietary supplement, however, and in late 2005 the FDA angrily acknowledged methyldrostanolone was being sold on the sports supplement market. In early 2006, the FDA sent letters to the manufacturer and a distributor demanding it be pulled from commerce. Superdrol has since been discontinued.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone is a modified form of dihydrotestosterone. It differs by: 1) the addition of a methyl group at carbon 17-alpha, which helps protect the hormone during oral administration, and 2) the introduction of a methyl group at carbon-2 (alpha), which considerably increases the anabolic strength of the steroid by heightening its resistance to metabolism by the 3-hydroxysteroid dehydrogenase enzyme in skeletal muscle tissue.

Side Effects (Estrogenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals. Since estrogen is the usual culprit with water retention, methyldrostanolone instead produces a lean, quality look to the physique with no fear of excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are major concerns.

Side Effects (Androgenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Although classified as an anabolic steroid,androgenic side effects are still possible with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Methyldrostanolone is a steroid with relatively low androgenic activity relative to its tissuebuilding actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone, methandrostenolone, or fluoxymesterone. Note that methyldrostanolone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.

Side Effects (Hepatotoxicity) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone is a cl 7-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. Cl 7-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. Note that although no human data can be found to make reference of, doses of 1 0 mg and 20 mg per day have been sufficient to produce high elevations of liver enzymes in consumers, as reported by private lab test results. Also, a small number of serious adverse events relating to liver toxicity have been reported with the use of this substance. The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.

Side Effects (Cardiovascular) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL cholesterol values and increase LDL cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Methyldrostanolone has a strong effect on the hepatic management of cholesterol due to its non-aromatizable nature, structural resistance to liver breakdown, and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. To help reduce card iovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.

Side Effects (Testosterone Suppression) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

Administration (Men) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methydrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. An effective dosage of methyldrostanolone for physique- or performance-enhancing purposes seems to begin in the range of 10-20 mg per day, taken for no longer than 6 or 8 weeks. At this level it seems to impart a measurable muscle-building effect, which is usually accompanied by fat loss and increased definition. Don't expect to gain 30 pounds on this agent (its name, which is short for "Super Anadrol," is more marketing than reality), but many do walk away with more than 10 pounds of solid muscle gain when using this agent alone. In determining an optimal daily dosage, some do find the drug to be measurably more effective when venturing up to the 30 mg range. Potential hepatotoxicity should definitely be taken into account with such use, however. To avoid further escalating liver strain, 20 mg daily of methyldrostanolone is sometimes stacked with a nontoxic injectable steroid, such as testosterone for massbuilding phases of training, or nandrolone or boldenone for more lean tissue gain and definition, instead of simply increasing the dosage. The drug also works well in cutting cycles, where its lack of estrogenicity is highly favored. Often it is combined here with a non-aromatizable injectable steroid like Primobolan or Parabolan.

Administration (Women) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall around 2.5 mg per day, taken in cycles lasting no more than 4-6 weeks to minimize the chance for virilization. The main point of contention with females is probably going to be the 10 mg product, which is far too high to use. Application would require splitting contents up into 4 separate doses. As with all steroids, virilization is still possible.
Code:
https://basicstero.ws
 
Hello, everyone!

We have some good news: we have restocked the domestic warehouse!

Here are PharmaSust 300, PharmaTest C, and a lot of Enanthate.

Furthermore, we now have our well-loved Oxandrolonos in the domestic US as well.
 
What’s going on with Meltos ? Is that discontinued from Pharmacom ? Will that be back ? How about Provironos will that be back ?
I was told Meltos is not currently being produced.
I'm not sure about the situation with Provironos; I'll have to ask the source about it.
 
I was told Meltos is not currently being produced.
I'm not sure about the situation with Provironos; I'll have to ask the source about it.
Is there any other items that are discontinued ? And whatever supply is left will be it until it runs out ?
I asked and have a reply.
No Proviron for now.
Provironos is not currently being produced.

As with any product, if stock is available it will show on the site and inventory will be sold until it all runs out.

I don't know of other items that are not in production currently (I assume everything that is currently stocked is still being produced).
But management makes the business decisions which depend upon factors such as demand and access to high-quality raws etc.
Remember when PRIMO-200 was not produced for a while; now I see PRIMO-200 is back in stock.

If there is any other specific item that has been out-of-stock for a long time and you would like me to ask them about, please let me know and I'll try my best to find out the current situation.
 
@RThoads @Pharmacom Support

I don't want to sound like a crazy person but why does you gear smell like flowers? It almost smells sweet like fruit or something...

I was injecting the other day and got a whiff of something, and placed my nose near the syringe and figured out that the oil was the culprit of this smell. Then I drew a drop from a vial of pharmacom EQ, Test C, Primo...I individually placed the drops on my fingers, rubbed the oil between my fingers and smelled it...all the oils smell floral or fruity or something...like lemon pledge or lysol...

Pardon the strange question but is there some sort of solvent that you use to make the oil smell like that?

Anyone else who has pharmacom gear on hand can you go smell your oil and tell me if I'm fucking nutso or not, please?
 
@RThoads @Pharmacom Support

I don't want to sound like a crazy person but why does you gear smell like flowers? It almost smells sweet like fruit or something...

I was injecting the other day and got a whiff of something, and placed my nose near the syringe and figured out that the oil was the culprit of this smell. Then I drew a drop from a vial of pharmacom EQ, Test C, Primo...I individually placed the drops on my fingers, rubbed the oil between my fingers and smelled it...all the oils smell floral or fruity or something...like lemon pledge or lysol...

Pardon the strange question but is there some sort of solvent that you use to make the oil smell like that?

Anyone else who has pharmacom gear on hand can you go smell your oil and tell me if I'm fucking nutso or not, please?

Just tested. It has some kind of floral smell compared to my hilma where i only smell the BA.

It think it’s the ethyl oleate


Ethyl oleate has a faint, floral note. Ethyl oleate occurs as a pale yellow to almost colorless, mobile, oily liquid with a taste resembling that of olive oil and a slight, but not rancid odor.
 
@RThoads @Pharmacom Support

I don't want to sound like a crazy person but why does you gear smell like flowers? It almost smells sweet like fruit or something...

I was injecting the other day and got a whiff of something, and placed my nose near the syringe and figured out that the oil was the culprit of this smell. Then I drew a drop from a vial of pharmacom EQ, Test C, Primo...I individually placed the drops on my fingers, rubbed the oil between my fingers and smelled it...all the oils smell floral or fruity or something...like lemon pledge or lysol...

Pardon the strange question but is there some sort of solvent that you use to make the oil smell like that?

Anyone else who has pharmacom gear on hand can you go smell your oil and tell me if I'm fucking nutso or not, please?
I thought it was all grape seed oil for these compounds
Hi, the odor depends on the composition, we use 5 to 10% pharmaceutical grade ethyl oleate in our oils. As a result injections are not painful and don`t cause big lumps, etc. (Attention shall be paid only with high concentrated oils 450-600 mg/ml! As carrier in all our vials is used grape seed oil.
 
Just tested. It has some kind of floral smell compared to my hilma where i only smell the BA.

It think it’s the ethyl oleate


Ethyl oleate has a faint, floral note. Ethyl oleate occurs as a pale yellow to almost colorless, mobile, oily liquid with a taste resembling that of olive oil and a slight, but not rancid odor.
Just tested. It has some kind of floral smell compared to my hilma where i only smell the BA.

It think it’s the ethyl oleate


Ethyl oleate has a faint, floral note. Ethyl oleate occurs as a pale yellow to almost colorless, mobile, oily liquid with a taste resembling that of olive oil and a slight, but not rancid odor.
Carrier oil for Pharmacom Labs oil products is GSO with small 5% to 10% EO.
Please see the source's site in the Innovations section under point number 5 linked in the "code" box below:
Code:
https://basicstero.ws/innovations
 
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