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凍結乾燥 · 10 mg / vial PT-141 (Bremelanotide) 10 mg / vial — HPLC検証済みペプチドバイアル
Sexual & Hormonal 10 mg / vial

PT-141 (Bremelanotide) 10mg — MC4R / MC3R Cyclic Peptide

Cyclic heptapeptide · Selective MC4R/MC3R · Sexual response pathway

Premium Grade

Cyclic heptapeptide melanocortin agonist — selective MC4R/MC3R activation in the sexual-response pathway.

CAS番号
189691-06-3
分子量
1 025.18 Da
純度
≥ 99.0% (HPLC)
保存
−20 °C、凍結乾燥
アミノ酸配列 Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
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本日お支払い $45 3バイアル・1本 $15
$59以上で無料米国向け $7.99(48時間)・世界向け $14.99(5営業日)
目立たない梱包目立たない断熱梱包、外部に化合物名なし。

分析証明書

ロット別分析報告書 — HPLC、ESI-MS、LALエンドトキシン、重金属、滅菌性

現在のロットPTM463
リリース済み2026-04-23
HPLC純度99.40%
エンドトキシン(LAL)合格 · < 0.5 EU/mg

PT-141 (Bremelanotide)について

Buy PT-141 (Bremelanotide) 10mg at IGF1 Shop. PT-141 is a synthetic cyclic heptapeptide derived from Melanotan II by replacing the C-terminal amide with a free carboxylic acid. This single change shifts receptor selectivity away from MC1R (melanogenesis) toward MC4 and MC3 receptors, producing distinct effects on sexual response pathways without significant tanning activity. Each PT-141 10mg vial is HPLC-verified at ≥99% purity, ESI mass-spec confirmed against the theoretical 1,025.18 Da molecular weight, and accompanied by a per-lot Certificate of Analysis. CAS 189691-06-3.

別名: PT-141 · PT 141 · Bremelanotide · Vyleesi

PT-141 (Bremelanotide) — 作用機序と仕様

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide derived from Melanotan II by replacing the C-terminal amide with a free carboxylic acid. This change shifts receptor selectivity toward MC4 and MC3 receptors, producing distinct effects on sexual response pathways without significant melanogenic activity.

品質とリリース基準

PT-141 (Bremelanotide)のすべてのロットは、逆相HPLC(参照標準に対して220 nmで面積純度≥ 99%)、分子量のESI質量分析確認、および0.5 EU/mg未満のLimulus Amebocyte Lysate(LAL)エンドトキシン試験に合格した後にのみリリースされます。ロット固有の分析証明書は注文に同梱され、購入前にリクエストに応じて提供可能です。

よくある質問

PT-141 (Bremelanotide) — よくあるご質問

What is PT-141?
PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide derived from Melanotan II by replacing the C-terminal amide with a free carboxylic acid. This change shifts receptor selectivity toward MC4 and MC3 receptors, producing effects on the sexual-response pathway without significant melanogenic activity. CAS 189691-06-3.
What is the standard PT-141 dose?
The standard PT-141 dose is 1.75mg subcutaneously, taken at least 45 minutes before activity. Maximum one dose per 24 hours, no more than 8 doses per month. A 10mg vial reconstituted with 1mL bacteriostatic water yields 1mg per 0.1mL — so a 1.75mg dose equals 0.175mL (17-18 units on a U-100 insulin syringe).
How fast does PT-141 work?
Onset is typically 30-60 minutes from subcutaneous injection, with peak effect at 2-4 hours and duration up to 8-12 hours. Effect varies by individual.
What side effects are common with PT-141?
The most frequently reported are mild facial flushing, transient blood pressure elevation, and nausea — particularly at first dose or higher doses. Effects typically attenuate with subsequent doses.
How is PT-141 tested?
Each PT-141 lot is HPLC-tested to ≥99% purity, ESI mass-spec confirmed, and LAL endotoxin tested below 0.5 EU/mg. ISO 17025-accredited third-party labs perform the testing.
How do I store PT-141?
Lyophilized PT-141 is stable at -20°C for 24+ months. After reconstitution with bacteriostatic water, store refrigerated at 2-8°C and use within 30 days.