Bestselling peptide raw material 99% high purity tizepatide

Solubility Soluble in DMSO Storage Store at -20°C

General tips For obtaining a higher solubility, please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.

Stock solution can be stored below -20℃ for several months.

Shipping Condition Secure Appearance: Powder Purity: >99% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: To be determined Shelf Life: >2 years if stored properly

Drug Formulation: To be determined

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

Tirzepatide (LY3298176) is a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist that is being developed for the treatment of type 2 diabetes. Tirzepatide (LY3298176) shows significantly better efficacy with regard to glucose control and weight loss than do Dulaglutide. Tirzepatide, also known as LY 3298176, is a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist. Tirzepatide has a greater affinity to GIP receptors than to GLP-1 receptors, and this dual agonist behavior has been shown to produce greater reductions of hyperglycemia compared to a selective GLP-1 receptor agonist. Signaling studies reported that tirzepatide mimics the actions of natural GIP at the GIP receptor. Tirzepatide was approved for improving blood sugar control in adults with type 2 diabetes, as an addition to diet and exercise.

Unlike traditional weight-loss drugs, it focuses on addressing the most stubborn visceral fat (VAT), making it particularly suitable for patients with HIV-related lipid metabolism disorders, helping to reshape a healthy body composition and waistline.

Four Core Benefits for a Healthy Physique

1. Targeted Fat Reduction: Directly Targeting the "Hidden Killer" Visceral Fat
Clinical data confirms that after 26 weeks of continuous use, visceral fat tissue (VAT) is significantly reduced by an average of 15%–24%.

It specifically targets stubborn fat deep within the abdomen that surrounds organs (such as buffalo hump, central obesity), rather than simply reducing subcutaneous fat or overall body weight.

2. Physiological Activation: Mimicking Natural Pulsating Secretion
By stimulating the pituitary gland, it prompts the body to secrete growth hormone (GH) in pulses, rather than directly supplementing with exogenous GH.

It is more in line with the body's natural rhythms, and hormone levels gradually decline after discontinuation, resulting in higher safety.

3. Metabolic Protection: Improves Blood Lipids and Liver Health Significantly reduces triglycerides and non-HDL cholesterol, optimizing blood lipid profile.

Multiple studies show it can reduce liver fat fraction and has potential anti-fibrotic protective effects in individuals with fatty liver disease (NAFLD/NASH).

4. Body Shape Optimization: Preserves Lean Body Mass, Prevents "Puffy Fat" While reducing harmful visceral fat, it helps maintain or increase muscle mass, preventing muscle loss during weight loss and resulting in a more toned and shapely physique.

Is tirzepatide available for weight loss?

It's also FDA approved for chronic weight management in adults with or without diabetes. Along with diet and exercise, tirzepatide can lead to significant weight loss — an average of 15% to 20% (34 lbs to 48 lbs). But tirzepatide for weight loss is only recommended for people who meet certain BMI criteria.

How fast do you lose weight on tirzepatide?

How quickly you lose weight depends on factors like lifestyle habits, diet, activity level, age, and other medications you may be taking. However, most people who follow a healthy diet and exercise routine begin reporting some weight loss within a month to two months of starting the medication.

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