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CJC

CJC-1295 (without DAC)

Short-Acting Growth Hormone Releasing Hormone Analog | Modified GRF 1-29

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What is CJC-1295 (without DAC)?

CJC-1295 (without DAC) is a lab-made analog of growth hormone-releasing hormone (GHRH), the body's natural signal that tells the pituitary gland to release growth hormone in bursts. Because this version clears the body quickly, researchers study it for restoring that natural, pulsatile release pattern rather than a sustained one. It's sold here strictly as a research chemical for laboratory study, not for use in people or animals.

Key terms:

CJC-1295 (without DAC) is a synthetic ghrh analog (mod grf 1-29).

CJC-1295 without DAC — also called Modified GRF 1-29, or Mod GRF 1-29 — is a lab-made version of growth hormone releasing hormone (GHRH), the body's own signal for releasing growth hormone. This short-acting form prompts growth hormone to come out in bursts, much like the body's natural pattern. Its half-life is only about 30 minutes, far shorter than the DAC-modified version. Researchers note that the short window allows finer control over each growth hormone pulse and lowers the chance that the receptor stops responding.

Key research areas

  • Preserves natural GH pulsatility
  • Minimal side effects
  • No receptor desensitization
  • Precise control over GH release

Researched dosing

This table reflects how researchers structure study designs with CJC-1295 — the dose ranges and schedules used in published research, presented as methodology reference, not usage instructions.

PhaseDoseFrequencyRoute
Longevity studies100mcg2x daily (morning and bedtime)Subcutaneous
Body-composition studies100-150mcg3x daily (morning, post-workout, bedtime)Subcutaneous
Highest-dose GH-release studies200mcg2-3x daily with GHRPSubcutaneous
Sleep studies100-200mcgOnce at bedtimeSubcutaneous

Commonly cycled 16 weeks on, 4+ weeks off.

How it works

At the cell level, CJC-1295 research looks at how the peptide binds GHRH receptors on the pituitary gland, prompting a burst of growth-hormone release similar to the body's own signaling pattern.

Binds to GHRH receptors on somatotroph cells, stimulating cAMP production and triggering growth hormone release in physiological pulses

Molecular data

These figures — molecular weight, amino-acid sequence, chain length — are the chemistry basics researchers use to confirm a CJC-1295 sample's identity and purity.

Weight
3367.97 Da
Length
30 amino acids
Type
GHRH analog (Mod GRF 1-29)

Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-Lys

Pharmacokinetics

This chart shows how quickly a research dose of CJC-1295 clears the body — notice the timescale is minutes, not days, which is why this version is studied for short, pulsatile GH release rather than sustained elevation.

Peak
0.25 hr
Half-life
0.5 hrs
Cleared
~2.5 hrs

Teichman et al. 2006

Research applications

This section lists the research areas scientists have studied for CJC-1295 — a summary of what's been investigated in the literature, not medical claims about people.

Growth Hormone

Most studied

Stimulates physiological growth hormone pulses that decline with age. Increases insulin-like growth factor 1 levels through enhanced GH secretion. Maintains healthy pituitary-somatotroph axis without suppression.

Longevity

Well studied

Supports longevity through restoration of natural GH pulsatility and IGF-1 elevation, improving body composition and tissue repair.

Recovery

Early research

Supports recovery from exercise and injury through enhanced growth hormone secretion and IGF-1 levels.

Dosage reference

Doses used in research
100 mcg per research dose (10 units at the common 100 mcg / 10 unit mixing ratio)
Frequency in studies
2-3 times daily for pulsatile release
Handling
Reconstituted solution — research use only; not for administration
Timeline reported in studies
GH elevation within 30 minutes, IGF-1 increases in 2-4 weeks, body composition changes in 6-12 weeks
Storage
Refrigerate immediately, use within 30 days of reconstitution
Cycle length
12-16 weeks continuous use
Break between cycles
Optional 2-4 week breaks to assess baseline

Interactions

This list shows which other growth-hormone-research peptides are studied alongside CJC-1295, and why they're often paired in published protocols.

Ipamorelin — synergistic GHRP-6 — synergistic GHRP-2 — synergistic Hexarelin — compatible CJC-1295 with DAC — compatible Tesamorelin — compatible MK-677 — compatible

Reconstitution & storage

This is the standard laboratory method for turning freeze-dried CJC-1295 powder into a liquid research solution.

  1. Allow vial to reach room temperature (15-20 minutes)
  2. Clean vial top with alcohol swab and allow to dry
  3. Calculate required bacteriostatic water volume using the calculator below
  4. Draw calculated volume of bacteriostatic water into syringe
  5. Inject water slowly down the inside wall of the vial (never directly onto powder)
  6. Gently swirl until powder completely dissolves (never shake)
  7. Solution should be clear - discard if cloudy or contains particles

Lyophilized: Room temperature, stable for 2 years if stored properly, use within 2 years

Reconstituted: 2-8°C, use within 30 days

Open the CJC-1295 reconstitution calculator

Quality indicators

These are the checks researchers and lab-report reviewers use to confirm a CJC-1295 sample is pure and correctly identified before it goes into a study.

Legitimate source with COA - Purchase from vendors providing certificates of analysis showing >98% purity

Proper cold chain shipping - Peptide should arrive with ice packs or refrigerated shipping in hot weather

Vacuum-sealed vials - Legitimate peptides create vacuum when reconstituted - water should be pulled in

Check expiration dates - Lyophilized peptide typically stable for 2 years if stored properly

Pre-mixed solutions - Avoid pre-reconstituted products - peptide degrades rapidly in solution

Discolored powder - White to off-white powder only - yellow or brown indicates degradation

What to expect

This timeline summarizes what the research literature reports at each study stage — research context for comparing studies, not a personal-results promise.

Day 1-7

Improved sleep quality, vivid dreams common due to enhanced REM sleep

Week 2-4

Increased recovery from workouts, reduced DOMS, better pumps

Week 4-8

Noticeable improvements in skin quality, minor body composition changes

Week 8-12

More significant lean mass gains, fat reduction, improved joint comfort

Week 12+

Continued gradual improvements in body composition and well-being

Safety notes

This section covers handling cautions and regulatory notes for CJC-1295 — research-use-only scope, not medical safety advice for people.

  • Not recommended for those with active cancer due to growth-promoting effects
  • Avoid if you have diabetic retinopathy or severe kidney disease
  • Monitor blood glucose if diabetic - GH can affect insulin sensitivity
  • Not FDA approved
  • Generally well-tolerated with minimal side effects at recommended doses

Regulatory status

  • Not approved by the FDA for any indication.
  • Supplied and described for laboratory research use only — not for human or veterinary use.

Community data

Community Poll

How would you rate your overall experience with this peptide?

1284 votes · Community data

Community Insights

82%reported positive results
68%noticed effects within 2 weeks
91%would recommend to others

Based on data the community reported. Not clinical proof.

References

  1. Animal model · Daily administration · 6 months

    No significant adverse effects on pituitary morphology or function with chronic use, supporting the safety of long-term pulsatile GHRH analog administration.

  2. In vitro + Human · Various doses · Receptor binding assays

    Found CJC-1295 without DAC had 4x greater receptor affinity than native GHRH and enhanced resistance to enzymatic degradation, a proposed explanation for its greater reported efficacy.

  3. Human · 100mcg 3x daily · 30 days

    Showed preservation of natural GH pulsatility patterns when administered 3 times daily, with no evidence of pituitary desensitization over the study period.