CJC-1295 (No DAC) + Ipamorelin

CJC-1295 (No DAC) + Ipamorelin

Total Price
$459.95
Discounted
$367.95
Vials
5
You Save
$92.00
20% OFF
Only $73.59 per vial— final price per vial after savings
Bulk pricing applied
📈 Upgrade to 10 vials and save an extra $184.00 vs buying 5 — nearly 5 free vials.
Selected Purchase Option:
  • 99%+ HPLC PurityIndependently verified by accredited US laboratory
  • Endotoxin-ScreenedLAL tested, LPS-free, endotoxin report available
  • GMP-Certified ManufacturingUSA facility, ISO 9001:2015
  • Lyophilized for StabilityShipped cold-packed, intact for reconstitution
Molecular Weight
Third Party Tested
Application
For Research Use only
Form
Lyophilized Powder
Storage
-20°C Long Term
Purity (HPLC)
99%+ Third Party Verified
Manufacture
USA / GMP

Description

CJC-1295 (No DAC) / Ipamorelin is a dual-peptide research blend combining two distinct synthetic compounds: a growth hormone-releasing hormone (GHRH) analogue and a selective ghrelin receptor agonist (growth hormone secretagogue). CJC-1295 without DAC is a modified 29-amino-acid peptide that mirrors the active fragment of endogenous GHRH, while Ipamorelin is a pentapeptide that engages the ghrelin/GHS-R1a receptor pathway independently. Together, they represent two complementary but mechanistically separate inputs into somatotroph signaling.

Because the two peptides operate through non-overlapping receptor classes, investigators use this blend to probe the additive or synergistic dynamics of pulsatile growth hormone (GH) release in controlled experimental systems. The absence of a Drug Affinity Complex (DAC) on the CJC-1295 component means the compound does not bind albumin for extended half-life, making it suitable for study designs that require discrete, time-resolved signaling pulses rather than continuous receptor activation.

The formulation is prepared under controlled manufacturing conditions and is characterized as a lyophilized, high-purity, endotoxin-tested blend. Low endotoxin content is a critical quality attribute for cellular and biochemical assay work, where lipopolysaccharide contamination can independently activate inflammatory pathways and confound experimental readouts. Batch-level endotoxin screening supports reproducibility across sensitive in vitro models.

Certificate of Analysis

Every batch is independently tested before it ships. Full documentation available for every product.

Lab Analysis — Vangaurd Testing Laboratory
HPLC Purity99%+ — Passes ≥99%
Mass Spectrometry IdentityConfirmed
Endotoxin (LAL)<1.0 EU/mg — LPS-Free
Sterility (USP)No growth detected
AppearanceLyophilized powder
Sequence ConfirmationAll confirmed
Content Quantification±0.2% — Within spec
Testing Lab AccreditationISO/IEC 17025:2017
ManufactureGMP / ISO 9001:2015
Analysis Date2026

Certificate of Analysis

Verified
99%+
HPLC Purity · This Batch
  • HPLC Separation: Exceeds 99% minimum
  • Mass Spectrometry: Molecular identity confirmed
  • Endotoxin Screen: <1.0 EU/mg — LPS-Free, LAL tested
  • Sterility: No microbial growth — USP compliant
  • Content: ±0.2% — accurate fill weight

Frequently Asked Questions

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