Buy CJC-1295 No DAC 5mg: B2B Procurement & Technical Whitepaper

Industrial Synthesis Specifications, Global Supply Chain Logistics, Quality Compliance & Research Grade Peptide Sourcing

cGMP Certified Purity ≥99.0% (HPLC) Mod GRF (1-29) Standard Lyophilized 5mg Vials Global Bulk API Export
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Technical Monograph

CJC-1295 No DAC 5mg (Mod GRF 1-29): Chemical Overview & Pharmacological Profile

CJC-1295 No DAC, clinically referred to as Modified GRF 1-29 (Mod GRF 1-29), is a synthetic tetrasubstituted 29-amino acid peptide analog of endogenous Growth Hormone-Releasing Hormone (GHRH). Engineered specifically to enhance metabolic stability while preserving physiological pulsatile signaling, CJC-1295 No DAC represents a vital benchmark standard in endocrinological research, peptide manufacturing, and scientific evaluation.

Unlike its long-acting counterpart containing the Drug Affinity Complex (DAC), CJC-1295 Without DAC omits the maleimido-propionic acid linker. This absence ensures that the peptide does not covalently bind to endogenous serum albumin, thereby maintaining a shorter, highly controlled half-life of approximately 30 minutes in physiological models. This distinct profile allows researchers to mimic physiological human growth hormone (hGH) pulses without inducing continuous, non-pulsatile receptor desensitization or chronic IGF-1 elevation.

Key Structural Insight: Mod GRF (1-29) incorporates four key amino acid substitutions relative to native GHRH (1-29): D-Ala at position 2, Gln at position 8, Ala at position 15, and Leu at position 27. These specific modifications protect the core sequence against rapid enzymatic cleavage by Dipeptidyl Peptidase IV (DPP-IV), dramatically elevating its chemical integrity in solution.

Molecular and Chemical Specifications Table

Parameter Specification Standard Analytical Method
Chemical Formula C152H252N44O42 Mass Spectrometry (MS-ESI)
Molecular Weight 3367.97 g/mol Calculated vs. Found MS
Sequence Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH2 Edman Degradation / MS Sequencing
Purity Level ≥99.0% (HPLC Area Peak) RP-HPLC (C18 Column)
Physical State Sterile Lyophilized Powder (White to off-white) Visual Inspection
Unit Packaging 5mg per Vial (Borosilicate Glass Vial Type I) Gravimetric Weight Control
Endotoxin Content <0.01 EU/mg LAL Kinetic Chromogenic Test
Counter-Ion Acetate (TFA exchange available upon bulk request) Ion Chromatography
Manufacturing Operations

Solid-Phase Peptide Synthesis (SPPS) & Purification Infrastructure

Commercial production of high-grade CJC-1295 No DAC 5mg requires precise adherence to advanced Solid-Phase Peptide Synthesis (SPPS) protocols under cGMP conditions. The complex 29-amino acid sequence demands strict control over coupling efficiency, steric hindrance mitigation, and racemization control.

Fmoc Protection Chemistry
Utilization of standard Fmoc/tBu protective strategies on high-capacity Rink Amide resin ensures complete C-terminal amidation. Coupling reagents such as HATU/DIPEA guarantee coupling rates exceeding 99.5% per cycle.
Prep-HPLC Purification
Crude peptides undergo dual-stage Preparative Reverse-Phase High-Performance Liquid Chromatography (RP-HPLC) utilizing dynamic axial compression columns to isolate the target fraction at ≥99% purity.
Cryogenic Lyophilization
Purified liquid fractions are transferred to Class 100 cleanroom environments for sterile filtration (0.22 μm) and deep vacuum freeze-drying to achieve stable, cake-structured 5mg vials with residual moisture <1.5%.

Comparative Analysis: CJC-1295 No DAC vs. CJC-1295 With DAC

When procuring GHRH analogs for research applications or retail distribution, understanding the pharmacokinetic differentiation between DAC and No DAC variants is vital for sourcing strategies:

  • Half-Life Profile: CJC-1295 No DAC exhibits a rapid clearance profile (~30 minutes), offering transient pituitary stimulation. CJC-1295 With DAC binds to serum albumin via its Lys-maleimide link, extending half-life to 6–8 days.
  • Secretory Pattern: No DAC promotes natural, pulsatile Somatotroph growth hormone releases. DAC provides continuous, basal GH elevation which may downregulate native receptor sensitivity over extended timelines.
  • Dosing Precision: The 5mg vial format for No DAC provides precise control over single or multi-dose experimental paradigms, making it the preferred standard for analytical research laboratories.
Enterprise Profile

About Gentolex Group & Global Operations

Creating global opportunities by connecting research institutions and pharmaceutical brands with guaranteed product quality and supply chain efficiency.

Global Footprint & Licensing

Gentolex’s goal is to create opportunities connecting the world with better services and guaranteed products. Up to date, Gentolex Group has been serving customers from more than 10 countries, specially, representatives are established in Mexico and South Africa. Our main services focus on supplying peptides APIs and Custom Peptides, FDF license out, Technical Support & Consultation, Product Line and Lab Setup, Sourcing & Supply Chain Solutions.

An overall factory construction area of 250,000 square meters under international standard allows us to offer flexible, scalable, and cost-effective solutions for clients globally.

Core Service Verticals
  • Chemicals & Peptides Products: High-throughput synthesis of raw APIs, protected amino acids, and custom peptide chains.
  • Pharmaceutical Ingredients: Extensive range of APIs and intermediates for development studies and commercial applications under cGMP compliance.
  • FDF License Out & Lab Setup: Complete technical transfer packages, validation documentation, and equipment sourcing for localized manufacturing setups.
  • Custom Procurement Services: Single-point procurement solutions to eliminate supply chain complexity for global clients.
250,000 m²
Factory Area
≥99.0%
Standard HPLC Purity
10+
Global Export Hubs
cGMP
Quality Standards
Supply Chain Intelligence

China OEM & Industrial Manufacturing Advantages

The global demand for high-purity peptides like CJC-1295 No DAC 5mg requires manufacturing partners capable of delivering uncompromised quality while maintaining robust batch-to-batch consistency and competitive production costs. Gentolex leverages China's advanced chemical manufacturing ecosystem to provide superior strategic procurement value.

Upstream Raw Material Integration
Direct access to domestic high-grade protected amino acid production reduces raw material sourcing lead times by 40% and shields B2B partners from international supply bottlenecks.
High-Capacity Lyophilization
Our modern 250,000 m² facility features automated multi-vial freeze-drying suites, capable of handling production runs from small pilot batches to multi-hundred-thousand vial commercial orders.
Strict Cold-Chain Packaging
All lyophilized CJC-1295 No DAC 5mg shipments utilize insulated cold-chain shipping protocols (-20°C ice gel packs) with temperature tracking to guarantee zero thermal degradation during transport.

Custom Packaging, Private Labeling & OEM Options

Gentolex offers full-spectrum OEM and ODM services for research chemical distributors, peptide brands, and institutional procurement agents:

  • Custom Vial Sizes: Available in 2mg, 5mg, 10mg, or custom bulk lyophilized powder quantities.
  • Flip-Off Cap Personalization: Custom logo embossing, color coding, and tamper-evident flip-off seals.
  • Analytical Documentation: Every batch is delivered with full Certificates of Analysis (CoA), High-Performance Liquid Chromatography (HPLC) chromatograms, and Mass Spectrometry (MS) verification reports.
Industry Vision

Technical Roadmap & Localized Market Applications

As global life sciences research shifts toward targeted endocrine therapies and metabolic regulation models, CJC-1295 No DAC continues to hold a prominent position in specialized application fields.

Localized Application Scenarios

In Vitro Cellular Assays
Used in academic and biomedical labs to investigate growth hormone receptor kinetics, signal transduction pathways (JAK2/STAT5), and somatotroph gene transcription mechanisms.
Combination Research Protocols
Frequently paired in scientific models with Ghrelin receptor agonists (such as GHRP-2, GHRP-6, or Ipamorelin) to analyze synergistic growth hormone release efficacy.

Future Technical Roadmap (2025–2030)

Gentolex remains committed to advancing synthesis automation and green chemical processing. Our strategic technical objectives include:

  • Green Peptide Synthesis: Transitioning to non-hazardous green solvents (e.g., 2-MeTHF, TEDA) in SPPS routines to minimize environmental impact while maintaining high yield.
  • Continuous-Flow Cleavage Technology: Implementing microfluidic cleavage systems to reduce trifluoroacetic acid (TFA) contact time, reducing side-chain degradation and improving raw crude purity to >85%.
  • Enhanced Counter-Ion Control: Expanding scalable non-TFA salt exchange capabilities (Acetate, Succinate, Citrate) to satisfy demanding formulation requirements.
Corporate Infrastructure

Gentolex Manufacturing Capabilities & Facilities

High-standard production plants and comprehensive supply chain solutions tailored for international clients.

Chemicals Products
An overall factory construction area of 250,000 square meters under international standard to offer flexible, scalable and cost-effective solutions.
Pharmaceutical Ingredients
Gentolex offers an extensive range of APIs and intermediates for development study and commercial application with cGMP standard from long-term collaborations. Documents and Certificates are supported to customers worldwide.
Development
Full lifecycle R&D support, analytical testing, HPLC purification, and customized peptide sequence engineering.
Procurement Service
For those clients who prefer to avoid the complexity of dealing with multiple points of contact, we provide extra customized procurement services with the most superior and comprehensive supply chain sources.
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Technical Insights

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Knowledge Base & FAQ

Frequently Asked Questions: CJC-1295 No DAC Procurement

Clear answers to technical, commercial, and shipping queries for prospective B2B purchasers and laboratory managers.

1. What is the difference between CJC-1295 No DAC and Mod GRF (1-29)?
CJC-1295 No DAC and Mod GRF (1-29) are terms used interchangeably in the scientific community. Both refer to the tetrasubstituted 29-amino acid sequence of GHRH without the maleimide Drug Affinity Complex. This specific molecular structure preserves pulsatile growth hormone secretion with a half-life of roughly 30 minutes.
2. How is CJC-1295 No DAC 5mg packaged and shipped to preserve stability?
Our CJC-1295 No DAC is supplied as a lyophilized (freeze-dried) powder in sealed 5mg Type I borosilicate glass vials. Lyophilized peptide vials are stable at ambient temperatures during transit for up to 2 weeks. However, cold-chain packaging (with gel ice packs) is utilized for long-distance international air freight. Upon arrival, long-term storage at -20°C is recommended.
3. What chemical analytical data is supplied with bulk wholesale orders?
Every batch of CJC-1295 No DAC manufactured by Gentolex is accompanied by a full Certificate of Analysis (CoA), containing Reverse-Phase High-Performance Liquid Chromatography (RP-HPLC) purity analysis showing ≥99.0% purity, Electrospray Ionization Mass Spectrometry (ESI-MS) mass verification, and endotoxin assay report (<0.01 EU/mg).
4. Can Gentolex provide custom branding or OEM packaging for 5mg vials?
Yes, Gentolex specializes in OEM/ODM custom solutions. We provide tailored flip-off caps (with custom logos), box packaging, custom vial sizes, specialized labeling, and white-label manufacturing tailored to your regional brand requirements.
5. What counter-ion options are available for bulk CJC-1295 No DAC API?
Standard lyophilized CJC-1295 No DAC is prepared as an Acetate salt. For specialized formulation needs, trifluoroacetate (TFA) removal and ion-exchange to Acetate or Hydrochloride (HCl) formats can be requested prior to bulk freeze-drying.
6. What is the minimum order quantity (MOQ) for B2B procurement?
MOQ depends on whether you are purchasing ready-to-ship standard batch vials or requesting custom OEM lyophilization runs. Standard inventory vials have low minimum order thresholds starting at 50 vials, while custom OEM runs begin at 1,000 vials per batch.
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