MSSPT PEPTIDE PEN 5 AMINI-1MQ PEN – R 1200
5-Amino-1MQ is a synthetic small-molecule compound with the chemical name 5-amino-1-methylquinolinium (also known as 5-amino-1-methylquinolin-1-ium). It is a positively charged heterocyclic molecule structurally related to quinolinium derivatives. Mechanism of Action
5-Amino-1MQ acts as a potent and selective inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme highly expressed in adipose tissue, liver, and certain metabolically active cells. NNMT catalyses the transfer of a methyl group from S–adenosylmethionine (SAM) to nicotinamide, producing 1–methylnicotinamide and S–adenosylhomocysteine (SAH). By inhibiting NNMT, 5-Amino-1MQ:
Reduces 1-methylnicotinamide production
Preserves intracellular nicotinamide levels
Increases NAD+ availability
Shifts cellular metabolism toward oxidative pathways
Enhances mitochondrial function and energy expenditure
Decreases fat storage and adipocyte differentiation
These effects support improved metabolic efficiency, reduced adipose tissue accumulation, and preservation of lean mass.
Indications & Usage
5–Amino-1MQ is used to support metabolic health and body composition. It is indicated for:
Promotion of fat metabolism and oxidation
Preservation of lean muscle mass during weight management
Support for energy expenditure and metabolic efficiency
Assistance in cellular energy homeostasis and anti-aging metabolic pathways
Contraindications & Warnings
Do not use if you have:
Known hypersensitivity to 5-Amino-1MQ or any excipient
Severe uncontrolled hypertension or cardiac arrhythmias
Active malignancy or history of hormone-dependent cancer
Severe hepatic or renal impairment
Age under 18 years
Pregnancy or breastfeeding
Warnings
Use only under medical supervision.
Monitor blood pressure, heart rate, and metabolic parameters during use.
Not a substitute for diet, exercise, or approved medical therapies for obesity or metabolic disorders. Discontinue immediately and seek medical attention if severe symptoms occur (e.g., rapid heartbeat, chest pain, severe headache, or signs of allergic reaction).
Dosage & Administration
Subcutaneous injection only.
Standard Dose: 5 mg (12 clicks) once daily
(1 click≈ 0.417 mg/417 mcg)
Alternative / Higher Dose (if tolerated): Up to 10 mg (24 clicks) daily
Frequency: Once daily
Timing: Morning, on an empty stomach (wait 30-60 minutes before eating) to optimize metabolic effects Cycle: 20 consecutive days on, followed by 2 weeks off (repeat as needed)
Administration Instructions
Wash hands and prepare a clean surface.
Attach a sterile needle.
Dial the required number of clicks (e.g., 12 clicks = 5 mg).
Clean injection site (abdomen or thigh) with alcohol swab.
Insert needle at 45-90° angle and inject slowly.
Withdraw needle, dispose safely, and cap the pen.
Rotate injection sites to minimize irritation.
Always inspect solution before use: Do not inject if cloudy, discoloured, or containing particles.
Side Effects
5–Amino-1MQ is generally well tolerated. Reported reactions are uncommon and usually mild/transient, including:
Mild injection-site irritation, redness, or itching
Transient headache or light-headedness
Temporary changes in energy levels or appetite
Rare mild gastrointestinal discomfort
If any severe or persistent symptoms occur (e.g., rapid heartbeat, severe headache, or signs of allergic reaction), discontinue use and contact your healthcare provider immediately.
Storage & Handling
Store either in refrigerator (fridge); never freeze or in a cool dry place (≤25-30°C / 77-86°F). Keep pen capped and protected from light and heat.
After first use: Same storage conditions.
Keep out of reach of children.
Discard if expired or solution appears abnormal.
Powered by Precision MSSPT
Peptide Pen formulations set the standard for research peptide delivery in challenging environments. Powered by exclusive MSSPT, each pen combines buffers, antioxidants, and proprietary agents in a compact, user-friendly injector, delivering strict control over pH, light, oxygen, oxidative factors, and moisture even under South Africa’s subtropical variability or the UAE’s extreme desert heat and humidity. This proprietary technology positions Peptide Pen as the premier choice for researchers in these regions: no mixing, no guesswork, and reliable, high-fidelity results despite demanding protocols and climates. Every Peptide Pen is built for exceptional durability, reliability, and performance, providing precision molecular stabilization in every dose, wherever your research takes you.
IMPORTANT NOTICE
This product is not intended to diagnose, treat, cure, or prevent any disease. Statements have not been evaluated by the FDA, SAHPRA, or other authorities. Always consult a licensed healthcare provider before use, especially if pregnant, breastfeeding, under 18, or managing medical conditions.
R750
GHRP-6 (Growth Hormone Releasing Peptide – 6) – 10mg per vial
Antiaging
Fat Burning
Inflammation
Injury
Muscle Recovery
Sleep
Fat loss. Muscle gain when used with anabolic steroid. Improved skin. Healing of injuries. Improved sleep. Reduction in Inflammation
Introduction
Research studies have shown that GHRP-6 stimulation of Growth Hormone secretion has a host of beneficial effects associated with increased growth hormone levels such as decreased body fat, increased muscle, and increased strength and stamina.
GHRP-6 is a peptide that has a wide range of potential benefits. It is commonly used by bodybuilders and athletes to help increase muscle mass and strength. Additionally, GHRP-6 has been shown to help promote healing and recovery from injuries. One of the most exciting potential applications of this peptide is its ability to help increase GH production. GH is a hormone that is essential for growth and development. However, GH levels decline as we age, which can lead to a decrease in muscle mass and strength, as well as an increased risk of age-related diseases.
GHRP-6 has been shown to stimulate GH production in both young and old individuals. In one study, this peptide was shown to increase GH levels by up to 400% in healthy young men (1). In another study, GHRP-6 was shown to increase GH levels by up to 34% in healthy elderly men (2).
In addition to its ability to increase GH production, GHRP-6 has also been shown to have several other potential benefits. For example, GHRP-6 has been shown to improve wound healing), increase bone density, and protect against liver damage.
GHRP-6 is a promising peptide with a wide range of potential benefits. However, more research is needed to fully understand its safety and efficacy.
GHRP-6 is a peptide that has a wide range of potential benefits. Researchers are still working to unlock all of its potential, but some of the potential benefits that have been identified so far include the following:
One of the most promising potential benefits of GHRP-6 is its ability to increase muscle mass. In one study, researchers found that rats who were treated with GHRP-6 saw an increase in muscle mass of up to 10%. While more research is needed to confirm these results in humans, they suggest that GHRP-6 could be a helpful tool for people looking to build muscle mass.
This peptide has also been shown to improve sleep quality. In one study, rats who were treated with GHRP-6 slept more soundly and for longer periods of time than those who were not treated with the peptide. While more research is needed to confirm these results in humans, they suggest that GHRP-6 could be a helpful tool for people looking to improve their sleep quality.
This peptide has also been shown to reduce inflammation. In one study, rats who were treated with GHRP-6 had reduced levels of inflammation markers in their blood. While more research is needed to confirm these results in humans, they suggest that GHRP-6 could be a helpful tool for people looking to reduce inflammation.
The use of GHRP-6 has been shown by researchers to improve healing. It helps in muscle repair during periods of deep sleep.
Side Effects
GHRP-6 is a peptide that has been shown to increase levels of growth hormone in the body. However, it is also associated with a number of side effects, including:
Increased appetite
Nausea
Headaches
Dizziness
Joint pain
Fatigue
Insomnia
Increased blood pressure
Increased heart rate
Anxiety
Depression
If you experience any of these side effects while taking GHRP-6, it is important to consult with your doctor.
Dosing Details
You inject 3ml water into the vial of GHRP 6 from the water vial. 1 full syringe is 1ml. You then wait for the vial powder content to dissolve ON ITS OWN.
DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out 10 (1 unit) on the syringe each morning before breakfast, 10 (1 unit) before lunch and 10 (1 unit) before bed and inject it into the tummy under the skin into the fatty skin layer. This is a total of 30 (3 units) on the syringe a day.
HD Labs HCG 5000iu (Human Chorionic Gonadotropin) is a glycoprotein hormone made up of 244 amino acids with a molecular mass of 36.7 kDa. It consists of two subunits: the α (alpha) subunit—shared with other hormones like LH, FSH, and TSH—and the β (beta) subunit, which is unique to HCG. Together, these subunits create a powerful hormone that plays a vital role in reproductive and hormonal health.
HCG interacts with LHCG receptors, supporting the maintenance of the corpus luteum during early pregnancy. This process helps stimulate progesterone production, enriching the uterus with blood vessels and nutrients to sustain fetal growth. Due to its highly negative charge, HCG may also help protect the fetus by repelling immune cells, contributing to maternal immune tolerance and supporting fetal implantation and development.
In addition to its reproductive functions, HCG plays a role in cell differentiation, tissue repair, and metabolic regulation. It can activate apoptosis (cell renewal) and may contribute to improved immune and cellular health.
1. Fertility Treatment
HCG is widely used in both men and women to support fertility:
In women, HCG triggers ovulation by mimicking luteinizing hormone (LH), which induces the release of mature eggs from the ovaries.
In men, HCG stimulates the Leydig cells in the testes to produce testosterone, which is vital for sperm production and fertility.
HCG is also used during IVF cycles to time egg retrieval and enhance progesterone production.
2. Hormonal Support and Hypogonadism
HCG therapy can help restore natural testosterone production in men with low testosterone (hypogonadism), supporting libido, energy levels, and muscle maintenance.
3. Tumor Marker and Diagnostic Use
HCG serves as a reliable tumor marker, as elevated levels may indicate certain cancers such as testicular cancer, choriocarcinoma, or germ cell tumors. When used alongside alpha-fetoprotein (AFP), it provides valuable data for cancer detection and monitoring.
4. Testing and Detection
HCG testing is the standard for confirming pregnancy, typically detected 6–12 days after ovulation. Blood tests can quantify HCG levels as low as 5 mIU/ml, offering early and accurate pregnancy confirmation.
HCG can be produced either by urinary extraction (from pregnant women) or through recombinant DNA technology. Brands like Pregnyl, Profasi, and Novarel use natural extraction, while Ovidrel represents recombinant HCG for enhanced purity and consistency.
HCG levels naturally vary throughout early pregnancy and can serve as indicators of embryo development and placental health. Abnormal levels may signal potential complications or disease states, making HCG monitoring essential in obstetric care.
In the past, HCG was promoted as a weight-loss aid under extremely low-calorie diets (popularized by Dr. Albert T.W. Simeons). However, modern medical evidence and official health organizations, including the Journal of the American Medical Association and The American Journal of Clinical Nutrition, have stated that HCG is not scientifically proven to promote weight loss or improve fat metabolism.
When used responsibly under professional medical supervision, HCG therapy may support:
Improved fertility and reproductive hormone balance
Restoration of natural testosterone levels in men
Enhanced sperm production
Support for luteal function in women
Regulation of progesterone for early pregnancy maintenance
Diagnostic applications for fertility and cancer detection
HD Labs HCG 5000iu offers a potent, medically significant formulation of Human Chorionic Gonadotropin, designed for clinical and therapeutic use under appropriate guidance. Its benefits in fertility, hormonal health, and diagnostic applications make it one of the most essential peptides in modern medicine.
Manufacturer’s Description:
Hgh fragment 177-191 is a stabilized analogue of the growth hormone-releasing factor (GRF) that induces Growth Hormone in a specific and physiological manner. To date, studies suggest that HGH Fragment 177-191 has several beneficial features: it reduces abdominal fat in particular visceral fat, without compromising glycemic control (blood glucose), it increases muscle mass and improves the lipid profile.
In one sentence – build lean muscle while burning excess fat.
Studies that can be found easily show that at a dosage of 500mcg, HGH Fragment 177-191 was shown to increase lipolytic activity in adipose tissue ,this HGH Fragment potently burns body fat, especially stubborn adipose body fat, and at the same time as it doesnt spike glucose levels, or cause any problems with insulin sensitivity, and improving your lipid profile, this really should be part of any dedicated athletes fat loss regime.
Unlike GH, HGH fragment doesnt induce cell proliferation, it does not induce hyperglycaemia or reduce insulin secretion. HGH fragment 177-191 does not compete for the hGH receptor, but of important note.. is the HGH Fragment’s ability to increase IGF-1 levels which translate into the HGH Fragment’s ability to give collateral anti-aging and anabolic effects along with its ability to induce fat loss in the most stubborn body fat (adipose tissue) while increasing energy expenditure and glucose and fat oxidation.
The dosage: 0.25mg, or 12.5 units on the insulin syringe (If you used 2ml water to mix it with). You inject once per day, either before exercise in the morning, or before bedtime at night. If your budget allows it, you can bump up the frequency to twice daily.
CJC1295 (With DAC) 2mg
Long-Acting Growth Hormone Releasing Peptide • Pharmaceutical-Grade Research Peptide
HD Labs CJC-1295 with DAC 2 mg is a high-purity synthetic peptide developed to pharmaceutical-grade standards for professional, clinical, and research environments. CJC-1295 with DAC (Drug Affinity Complex) is designed to prolong growth hormone–releasing activity by extending the peptide’s half-life in circulation.
HD’s advanced manufacturing and strict quality-control processes ensure a stable, consistent, and reliable peptide suitable for long-acting endocrine research applications.
Melanotan II (MT-II) is a synthetic, cyclic heptapeptide analogue of the naturally occurring α-melanocyte-stimulating hormone (α-MSH). It acts as a non-selective agonist of the body’s melanocortin receptors (primarily MC1R, MC3R, MC4R, and MC5R).
In scientific and preclinical research, MT-II is primarily studied for its potent influence on systemic pigmentation (melanogenesis) and its secondary effects on metabolic rate, appetite suppression, and sexual function.
Key Research Mechanisms & Benefits
1. Advanced Melanogenesis (Skin Pigmentation)
By binding directly to MC1R receptors on melanocytes, Melanotan II stimulates the production of eumelanin (the dark brown-to-black pigment responsible for skin color) rather than pheomelanin (yellow-to-red pigment).
UV-Independent Pigmentation: Research indicates it induces skin darkening even in the absence of direct ultraviolet radiation, though the process accelerates when paired with minimal UV exposure.
Photoprotective Studies: Because eumelanin physically scatters UV light and scavenges free radicals, MT-II is widely investigated for its potential to protect fair-skinned or phototype-vulnerable subjects from sunburn and UV-induced DNA damage.
2. Appetite Suppression and Metabolic Shifts
By interacting with MC4R receptors in the central nervous system, MT-II mimics the body’s natural satiety pathways. In animal models, this results in significant acute appetite suppression and an upregulation of lipid metabolism, aiding in fat tissue loss.
3. Modulation of Sexual Function
Activation of central melanocortin pathways (specifically MC3R and MC4R) has been shown to induce erectile responses and increase libido through mechanisms entirely independent of the vascular nitric oxide system.
Theoretical Dosing Protocols (Research Use Only)
Important Regulatory & Safety Disclaimer: Melanotan II is an experimental research compound. It is not approved for human consumption, diagnostic procedures, or therapeutic use by the FDA, SAHPRA, or any international regulatory authorities. This profile is compiled strictly for educational and laboratory research purposes.
Melanotan II possesses high systemic bioavailability and is typically administered via subcutaneous (SQ) injection into adipose tissue using a standard insulin syringe.
Protocols in literature are strictly divided into two phases to prevent sudden hyper-pigmentation or extreme side effects:
Phase 1: The Loading Phase (Acclimatization & Pigment Building)
The goal of the loading phase is to gradually introduce the peptide to build tolerance and steadily upregulate melanin production.
Standard Daily Dosage: 100 mcg to 250 mcg once per day.
Protocol Practice: Researchers frequently start at a micro-dose of 50 mcg to 100 mcg on Days 1–3 to evaluate systemic sensitivity before adjusting upward toward a standard 250 mcg dose.
Duration: Run daily for 7 to 14 days, or until the target pigment density is achieved.
Phase 2: The Maintenance Phase (Color Preservation)
Once the desired pigmentation level is achieved, daily administration ceases to avoid progressive over-darkening.
Standard Weekly Dosage: 500 mcg to 1,000 mcg (1 mg) total per week.
Frequency: Split evenly into 1 to 2 injections per week (e.g., 250 mcg to 500 mcg per injection).
Reconstitution Math & Syringe Calibration
Melanotan II is highly stable in its lyophilized (freeze-dried) state but breaks down quickly once liquid is introduced. It is typically distributed in 10 mg vials.
Reconstitution Formula
Adding 2 mL of Sterile Bacteriostatic Water to a 10 mg vial creates a concentration of 5 mg per 1 mL. On a standard U-100 insulin syringe, the breakdown correlates as follows:
10 Units (0.1 mL) = 500 mcg
5 Units (0.05 mL) = 250 mcg
2 Units (0.02 mL) = 100 mcg
Storage and Handling
Mixing: Slowly trickle the bacteriostatic water down the internal glass wall of the vial. Do not shake or agitate the vial aggressively to avoid fracturing the peptide structure.
Temperature: Keep unmixed vials frozen at -20°C. Once reconstituted, store exclusively in a dark refrigerator at 2°C to 8°C and utilize within 30 days.
Documented Side Effects & Considerations
Due to its non-selective binding across multiple melanocortin receptors, MT-II exhibits several acute side effects that researchers must carefully monitor:
Nausea & Appetite Loss: Mild to severe acute nausea frequently occurs within 20–30 minutes post-injection (often mitigated by administering the dose immediately before sleep).
Flushing & Spontaneous Yawning: Temporary facial flushing, increased heart rate, and involuntary stretching/yawning are common due to central nervous system activation.
Hyperpigmentation & Mole Darkening: Existing moles, freckles, and scar tissue will darken significantly faster than surrounding skin. New micro-hyperpigmentation spots (“melanotan freckles”) can temporarily appear.
Priapism: Prolonged or unwanted erections can occur, especially if loading doses exceed recommended thresholds.
HD Labs BPC 157 5 mg, is a peptide with a growing reputation for its potential therapeutic benefits and limited side effects. Below, we explore the advantages, potential side effects, detailed dosage instructions, and half-life associated with BPC157.
Benefits of BPC157 (5mg):
Tissue Healing: BPC157 may accelerate the healing of various tissues, including muscles, tendons, ligaments, and even organs. It promotes tissue regeneration and repair, which may help individuals recover from injuries more swiftly.
Reduced Inflammation: BPC157 exhibits anti-inflammatory properties, potentially mitigating the inflammation associated with injuries or certain medical conditions.
Pain Management: Users have reported a reduction in pain and discomfort, particularly in cases of musculoskeletal injuries and joint issues.
Gastrointestinal Health: BPC157 may contribute to the maintenance of gastrointestinal health by aiding in the repair of the gut lining and potentially alleviating digestive issues.
Dosage Instructions:
Dosage instructions for BPC 157 (5mg) can vary based on individual needs and the advice of a healthcare provider. BPC157 is typically administered via subcutaneous or intramuscular injections. Here are general guidelines:
Dosage: Common dosages range from 250 to 500 micrograms (µg) per day, divided into multiple injections.
Injection Frequency: Typically, a user administers BPC 157 5 mg injections once or twice a day.
Duration of Use: The duration of use may vary, but healthcare providers often recommend using BPC 157 for several weeks to months, followed by periods of rest.
It is crucial to consult with a qualified healthcare provider before starting a BPC157 regimen to determine the appropriate dosage and duration of use based on individual health needs.
Side Effects:
BPC 157 5 mg is generally considered safe and well-tolerated. However, like any substance, it may have potential side effects, which are typically mild and infrequent. These may include:
Injection Site Reactions: Users may experience minor irritation, redness, or swelling at the injection site.
Gastrointestinal Issues: Some individuals have reported mild digestive discomfort, but this is relatively rare.
Allergic Reactions: Although rare, allergic reactions are possible, so users should monitor for signs such as hives or difficulty breathing.
It’s essential to remember that side effects can vary among individuals, and severe adverse effects are uncommon.
Half-Life:
BPC157 has a relatively short half-life, estimated to be approximately 2-3 hours. This means that the body rapidly metabolizes and clears it. As a result, healthcare providers typically recommend multiple daily injections to maintain consistent levels of BPC157 in the bloodstream.
In summary, BPC157 (5mg) is a peptide with potential therapeutic benefits, particularly in tissue healing, inflammation reduction, pain management, and gastrointestinal health. Limited side effects can occur, but it is generally considered safe. Proper dosage instructions and guidance from a healthcare provider are crucial for those considering BPC157 as part of their treatment regimen.
Important Information
This product is supplied in a lyophilised peptide format
Consultation with a licensed healthcare provider is essential prior to any consideration of use
Results observed in clinical trials may not reflect real-world outcomes
PT-141 (Bremelanotide) is a synthetic peptide developed to treat sexual dysfunction in men and women by activating the brain’s melanocortin receptors (MC3 and MC4). Unlike Viagra or Cialis, which enhance blood flow to the genitals, PT-141 stimulates the part of the brain responsible for sexual arousal, leading to heightened desire, improved performance, and increased satisfaction. It is used by both men seeking improved erectile function and women aiming to enhance libido and sensitivity. Results are typically felt within 30–60 minutes after injection and can last up to 72 hours.
Benefits of PT-141:
Increases sexual desire and libido in both men and women
Enhances arousal and sensitivity
Improves erectile function in men
Promotes stronger and more satisfying sexual experiences
Works neurologically rather than through vascular pathways
Side Effects of PT-141:
Temporary nausea or flushing
Mild headache
Occasional dizziness
Rare increase in blood pressure
Dosages & Protocol:
Men and Women: Start with 1mg (0.1ml) injected subcutaneously 30–60 minutes before anticipated activity.
Advanced users may increase to 2mg (0.2ml) based on individual tolerance and response.
Do not exceed one dose within a 24-hour period.
Description
TB-500 is a synthetic version of the naturally occurring peptide present in virtually all human and animal cells, Thymosin Beta 4 (T?4). It is a first-in-class peptide candidate that promotes the following*: Endothelial (blood vessels) cell differentiation Angiogenesis (growth of new blood cells from pre-existing vessels) in dermal tissues Keratinocyte migration Collagen deposition; and Decreases inflammation.
TB-500 offers many benefits to the equine world in performance racing. Recent trials by some of the world?s leading trainers on their prize winning equine members of both genders, have been credited by a huge boost in their race-day results, something long desired in the racing world. These trials along with clinical trials have indicated the following benefits associated with the use of TB-500 on mares and stallions: Increase muscle growth with huge increases in endurance and strength noted Relaxed muscle spasm Improved muscle tone Increase the exchange of substance between cells Encourage tissue repair Stretches connective tissue Helps maintain flexibility Reduces inflammation of tissue in joint Enhances nutritional components in the animal Prevents the formations of adhesions and fibrous bands in muscles, tendons and ligaments. When these proven benefits are viewed in conjunction with the fact that 60% of a horse?s body weight is muscle, it is clear to see the full potential of TB500 can be reviled in by majority of the horse?s body. In a racing era that surrounds itself around gaining that competitive edge through the use of various substances, none will deliver the results that will be experienced with the use of TB-500. Perhaps the greatest selling point of the product is that it?s 100% DRUG FREE and DOES NOT SWAB. This allows the peptide to be used right throughout racing spells in both training and competition completely free of any banned substance.
5-Amino-1MQ is a research compound known as an NNMT inhibitor. By blocking the NNMT (nicotinamide N-methyltransferase) enzyme, it prevents fat storage, reduces fat cell size, and boosts NAD+ levels—resulting in improved energy metabolism and body composition.
Primary benefits includes
Accelerated Fat Loss: By blocking NNMT, the compound stops cells from slowing down their metabolism and encourages the body to use stored fat for energy.
Enhanced Muscle Strength & Recovery: Preclinical studies indicate that inhibiting NNMT can improve grip strength and endurance, and aid in the rapid regeneration and healing of muscle tissue.
Improved Metabolic Function: By optimizing cellular energy and increasing NAD+, it helps balance blood sugar and improves overall insulin sensitivity
Anti-Aging & Cellular Repair: Increased NAD+ activates sirtuins (the “longevity genes”), which combat cellular aging, reduce inflammation, and promote mitochondrial health.Increased Energy (Without Stimulants): It boosts ATP production at the cellular level, leading to higher natural energy and focus without the jitters associated with traditional stimulants.