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CJC-1295 / Ipamorelin

growth-hormone

CJC-1295 / Ipamorelin

Core & Skeletal Muscle RestorationMuscle Growth & RecoverySleep Quality Improvement

A precision-formulated blend pairing a sustained-release GHRH analogue with a highly selective ghrelin mimetic — designed for amplified, pulsatile growth hormone stimulation without cortisol or prolactin spillover.

For research and laboratory use only. Not for human consumption.

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Technical Data

Specifications

Specifications

Technical Details

01
Purity≥99% (HPLC, each component)
02
FormLyophilized Powder
03
StorageStore at -20°C. Reconstituted: 2–8°C, use within 14 days.
04
DosageCJC-1295: 2 mg 1–2x/week; Ipamorelin: 100–300 mcg per dose in research models
05
FormatCo-lyophilized blend
06
SourceSynthetic (both components)
07
MechanismGHRH receptor + GHS-R1a dual agonism
08
CJC-1295 MW3647.28 Da (DAC form)
09
CJC-1295 CAS863288-34-0
10
Ipamorelin MW711.86 Da
11
Ipamorelin CAS170851-70-4

Bulk Pricing

Volume Pricing Guide

QuantityPrice PerSavings
1$162
2 - 4$14610% off
5 - 9$13815% off
10 - 14$13020% off
15 - 19$12225% off
20+Best Value$11330% off

Quality Assurance

Certificate of Analysis

Certificate of Analysis

BatchDL8405
Purity98.9% (HPLC)
Test Date2024-06-28
LabDarmerica (Davie, FL)

Research Overview

About CJC-1295 / Ipamorelin

CJC-1295 is a synthetic growth hormone-releasing hormone (GHRH) analogue that employs Drug Affinity Complex (DAC) technology to achieve covalent albumin binding in circulation, extending its biological half-life from minutes to approximately 6–8 days. This sustained presence enables continuous stimulation of pituitary somatotrophs and prolonged elevation of both growth hormone and IGF-1 levels in research models.

Ipamorelin is a pentapeptide growth hormone secretagogue receptor (GHS-R1a) agonist that triggers GH release through the ghrelin signaling pathway — mechanistically independent of GHRH. Its defining characteristic is selectivity: unlike earlier secretagogues such as GHRP-6, ipamorelin stimulates growth hormone release with minimal concomitant increases in cortisol, prolactin, or ACTH, producing a cleaner pharmacological profile.

The combination leverages convergent signaling on somatotroph cells — simultaneous GHRH receptor and ghrelin receptor activation produces synergistic GH pulse amplification exceeding either agent alone. ROEHN supplies this blend at 99% HPLC-verified purity (each component) as a co-lyophilized powder, supporting research into IGF-1 kinetics, body composition, sleep architecture, and recovery in aging and performance models.