Peptuno
GH-Axis Peptides
Featured

Product details

HGH Fragment 176-191 is the unmodified 16-amino-acid C-terminal fragment of native human growth hormone, corresponding to residues 176-191 of the full-length 191-amino-acid HGH protein. The fragment retains the lipolytic activity associated with this region of native HGH while lacking the central regions that mediate the broader anabolic and IGF-1-stimulating effects of full-length GH. Distinct from the AOD9604 modified analog (which adds an N-terminal tyrosine for iodination-tracking purposes), HGH Fragment 176-191 is the unmodified native sequence and is the form typically used in research workflows studying the lipolytic activity of the HGH C-terminal region in isolation from the rest of the molecule.

Peptuno supplies HGH Fragment 176-191 at ≥99.0% HPLC purity with full identification: CAS 66004-57-7, formula C78H123N23O22S2, MW 1799.1 g/mol, sequence FLRIVQCRSVEGSCGF (note the two cysteines at positions 7 and 14 that can form an intramolecular disulfide bridge under oxidative conditions). The disulfide-bridging behavior is the most common identity-confirmation concern, the reduced and oxidized forms differ by 2 Da and elute at different RP-HPLC retention times. Six standard fill sizes (1-15 mg) cover most research and compounding workflows.

Regulatory note: Easily confused with AOD9604 (the modified analog with N-terminal tyrosine). Confirm exact fragment identity (unmodified vs. AOD9604-modified) via batch COA before order placement; the two are not chemically equivalent.

FAQ

How do I distinguish HGH Fragment 176-191 from AOD9604 at the analytical level?
The two molecules differ at the N-terminal residue: native HGH Fragment 176-191 starts with phenylalanine (FLRIVQCRSVEGSCGF), while AOD9604 is Tyr-hGH(177-191) (YLRIVQCRSVEGSCGF), where a tyrosine replaces that N-terminal phenylalanine. Both are 16-amino-acid peptides; HGH Fragment 176-191 has theoretical MW 1799.1 Da and AOD9604 ≈1815 Da. The mass difference is only about +16 Da (the Tyr side chain carries one extra oxygen versus Phe), so the diagnostic mass-spec check at first-time supplier qualification needs adequate resolution. RP-HPLC retention time is also slightly different, the more polar AOD9604 (with the Tyr hydroxyl) elutes slightly differently under typical conditions. Buyers should always confirm the released-batch mass against the expected mass for the form they ordered, since the molecules are easy to confuse but biologically distinct.
What does the intramolecular disulfide bond in HGH Fragment 176-191 mean for handling?
The 176-191 sequence (FLRIVQCRSVEGSCGF) contains two cysteines (positions 7 and 14 within the fragment) that can form an intramolecular disulfide bond. Under reducing conditions during synthesis, the cysteines are free thiols; under oxidative conditions during storage and reconstitution, they can form the disulfide bridge. The reduced and oxidized forms differ by 2 Da in mass and elute at different RP-HPLC retention times. Most published research uses the oxidized (disulfide-bridged) form, which is the more stable solid-state form. Buyers should confirm with the COA which form the batch represents, if your research protocol requires a specific form, this matters operationally.

Certificate of Analysis (COA)

The per-lot COA for this product will appear here.

Related products