CJC 1295 No DAC 5 mg/Ipamorelin 5 mg CJC 1295 No DAC 5 mg/Ipamorelin 5 mg
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CJC 1295 No DAC 5 mg/Ipamorelin 5 mg

Growth Hormone-Releasing Hormone & GHRP Blend

  • Substance:
     - CJC 1295 (No DAC) 5 mg
     - Ipamorelin 5 mg
  • Strength: 10 mg/vial
  • Form: Lyophilized powder
  • Packaging: 2 mL glass vial
  • Manufacturer: Dragon Pharma, Europe
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Dragon Pharma CJC 1295 No DAC/Ipamorelin

CJC 1295 No DAC/Ipamorelin 10 mg delivers a precisely formulated research blend of two of the most synergistic peptides for stimulating the body's natural growth hormone (GH) production. This combination pairs CJC 1295 (without Drug Affinity Complex/DAC)—a potent Growth Hormone-Releasing Hormone (GHRH) analog—with Ipamorelin, a selective Growth Hormone-Releasing Peptide (GHRP). Together, they create a powerful dual-pathway approach: CJC 1295 No DAC mimics the natural hypothalamic signal to the pituitary gland to release GH, while Ipamorelin provides a complementary signal through a different receptor pathway (ghrelin receptor), while also inhibiting somatostatin (the hormone that suppresses GH). This results in a robust, synergistic amplification of natural GH pulses without the long-term, non-pulsatile elevation associated with CJC 1295 WITH DAC.

For bodybuilders, athletes, and anti-aging researchers in the USA, Dragon Pharma's CJC 1295 No DAC/Ipamorelin blend represents a sophisticated research tool for studying body recomposition, recovery, and performance. By promoting natural, pulsatile GH secretion, research suggests this combination may support increased muscle protein synthesis, enhanced fat metabolism, improved sleep quality, accelerated injury recovery, and better skin elasticity—all benefits associated with optimal GH levels. The "No DAC" version of CJC 1295 is preferred for research aiming to mimic the body's natural circadian GH rhythm. Manufactured by Dragon Pharma in certified European facilities, each vial contains a carefully balanced 5 mg/5 mg ratio of high-purity peptides as a lyophilized powder, ensuring consistency and reliability for scientific investigation.

Key Benefits:

  • Synergistic GH Stimulation: Dual-action formula amplifies natural growth hormone pulses through both GHRH and GHRP pathways for potent research outcomes.
  • Pulsatile & Physiological: The "No DAC" version promotes natural, short-lived GH pulses that mimic the body's healthy endocrine rhythm, avoiding constant elevation.
  • Selective & Clean Mechanism: Ipamorelin is highly selective for GH release with minimal effect on cortisol or prolactin, offering a cleaner research profile.
  • Enhanced Recovery & Body Composition: Research focuses on potential benefits for muscle growth, fat loss, connective tissue repair, and improved sleep architecture.
  • Convenient Pre-Mixed Blend: The 5 mg/5 mg ratio is optimally balanced for research, eliminating the need to source and mix two separate peptides.

Each 2 mL vial contains 5 mg of CJC 1295 (No DAC) and 5 mg of Ipamorelin (10 mg total blend) as a sterile lyophilized powder, manufactured under strict quality control standards in Dragon Pharma's certified research facilities.

Product Specifications

Product Name CJC 1295 No DAC/Ipamorelin
Manufacturer Dragon Pharma
Substance CJC 1295 (No DAC) + Ipamorelin
Packaging 2 mL glass vial, lyophilized powder blend
Lab Test Result 5.93 mg CJC / 4.96 mg Ipa (Nov 2025 batch)
Half-Life CJC 1295 No DAC: ~30 min; Ipamorelin: ~2 hours
Recommended Cycle Research cycles typically range from 8-12 weeks, often followed by a break to prevent receptor desensitization.
Form Lyophilized (freeze-dried) powder blend for reconstitution
Aromatization Not applicable (non-hormonal peptides)
Dosage (Research Models) Typically studied with 1-3 daily administrations to mimic natural GH pulses (morning, post-workout, before bed).

Usage Guidelines

For Laboratory Research Only: This information summarizes scientific literature. Dragon Pharma CJC 1295 No DAC/Ipamorelin is a research chemical for in vitro or preclinical study, not for human use.

In experimental models, the blend is reconstituted with bacteriostatic water. Research often utilizes subcutaneous administration. To mimic the natural pulsatile secretion of GH, study designs frequently split the daily dose into 2-3 administrations (e.g., morning, post-training, pre-bedtime). This timing aligns with the body's natural GH surge periods. Research cycles are typically limited to 8-12 weeks to minimize potential downregulation of pituitary receptors. Administration on an empty stomach (or at least 2 hours post-meal) is common in protocols to avoid interference from food-induced insulin and somatostatin.

  • Standard Pulsatile Research Cycle (8-10 weeks): Twice or thrice-daily dosing protocol to study effects on body composition, recovery markers, and sleep quality, followed by a 4-week off period.
  • Extended Recovery & Anti-Aging Study (12 weeks): Longer cycle focusing on cumulative benefits for skin, joint health, and metabolic parameters, often with careful monitoring of fasting glucose.

Post Cycle Therapy (PCT):

As peptides that stimulate endogenous GH, this blend does not suppress the HPTA, so traditional PCT with Clomid is unnecessary. The primary research consideration is pituitary receptor sensitivity. A break of at least 4 weeks between cycles is standard to allow receptor recovery. Some research protocols may incorporate a GHRH like Sermorelin during the off-period to maintain gentle stimulation. For comprehensive hormonal support research post-cycle, Enclomiphene could be studied for testosterone optimization.

Synergistic Research & Support:

This GH-stimulating blend is often researched alongside other compounds for body recomposition. For studying muscle growth synergy, it can be paired with SARMs like LGD 4033. For enhanced fat loss research, combining with Tesamorelin (a different GHRH) or AOD 9604 could be explored. To support joint and connective tissue health during intense training studies, adding TB-500 may be relevant.

Third-Party Lab Tested

Dragon Pharma CJC 1295 No DAC/Ipamorelin Lab Test Result November 2025
2025-11-07
5.93 mg/4.96 mg

Lab Analysis: The November 2025 third-party HPLC test confirms 5.93 mg of CJC 1295 (No DAC) and 4.96 mg of Ipamorelin per vial, totaling 10.89 mg with a precise 1.19:1 ratio. This demonstrates excellent batch consistency, high purity for both peptides, and accurate blending—exceeding the labeled 10 mg total content.

Storage Instructions

Proper storage is essential to preserve the stability of this peptide blend.

  • Unreconstituted Powder: For long-term stability, store the sealed vial in a freezer at -20°C (-4°F) or colder. The lyophilized blend remains stable for up to 24 months under these conditions. Avoid repeated freeze-thaw cycles and protect from light.
  • After Reconstitution: Once reconstituted with bacteriostatic water, the solution must be refrigerated immediately at 2°C to 8°C (36°F to 46°F). The refrigerated solution is typically viable for research for 3-4 weeks. For studies using multi-daily dosing, maintaining strict refrigeration is critical. Never freeze the reconstituted liquid.
  • Important Note: Due to the differing stabilities of the two peptides, it is recommended to use the reconstituted solution within 21 days for optimal research results. Always use sterile technique.

What is the difference between CJC 1295 with DAC and No DAC?

CJC 1295 WITH DAC (Drug Affinity Complex) binds to albumin, creating a very long half-life (several days) that results in a constant, elevated level of GH. CJC 1295 NO DAC has a short half-life (~30 min), producing sharp, pulsatile GH releases that more closely mimic the body's natural secretion pattern. The "No DAC" version is preferred in research aiming for physiological, rhythmic stimulation.

Why combine CJC 1295 No DAC with Ipamorelin?

They work synergistically through different mechanisms. CJC 1295 is a GHRH analog that signals the pituitary directly. Ipamorelin is a GHRP that works through the ghrelin receptor and also inhibits somatostatin (which blocks GH release). Together, they provide a stronger, more complete signal for GH release than either peptide alone, creating a potent research combination for studying GH effects.

What are the main research applications for this blend?

Primary research focuses include: 1) Body recomposition studies (muscle growth and fat loss synergy), 2) Recovery and injury healing models (enhanced collagen synthesis), 3) Sleep quality and architecture research, 4) Skin elasticity and anti-aging parameters, and 5) Metabolic health markers like insulin sensitivity and lipid profiles.

How long does it take to see effects in research models?

Subjective effects like improved sleep and recovery may be noted in studies within the first 1-2 weeks. Measurable changes in body composition (reduced body fat, increased lean mass) typically become statistically significant after 4-8 weeks of consistent administration in a controlled research protocol. Full benefits on connective tissues and skin may take 12+ weeks to manifest in study outcomes.

Is the Dragon Pharma blend accurately dosed?

Yes. The latest third-party lab test (Nov 2025) shows 5.93 mg of CJC 1295 No DAC and 4.96 mg of Ipamorelin, totaling 10.89 mg with high purity for both peptides. This exceeds the labeled 10 mg total and confirms precise, consistent blending. Dragon Pharma's commitment to transparency and quality ensures researchers receive a reliable, accurately formulated product.

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