Research Scientific
ULTIMATE GradeADIPOTIDE (FTPP)
Research-grade peptide · Individual vials
Product reference: PEP007U
Our ULTIMATE research-grade option. Review the product-specific specification and supporting batch records for the additional quality requirements.
- Grade
- ULTIMATE
- Purchase format
- Individual vial
- Presentation
- Lyophilised powder
What you are ordering
This listing is for ULTIMATE Grade ADIPOTIDE (FTPP) in individual vials. Select your required option using the product controls. The declared quantity applies to one vial, not to a multi-pack. This is not the Regular Grade listing.
Chemical information
- Synonym in the supplied description
- Da-74204; requires manufacturer confirmation.
- Chemical Abstracts Service registry number, as supplied
- 859216-15-2.
- Molecular formula, as supplied
- C₁₁₁H₂₀₆N₃₆O₂₈S₂.
- Approximate molecular mass in the supplied description
- 2,554 daltons; subject to the clarification below.
- Physical presentation
- Lyophilised laboratory powder.
- Purity specification
- No numerical purity is specified in the supplied description. Refer to a completed, batch-specific Certificate of Analysis for the analytical method, acceptance criterion and reported result.
Chemical-information clarification: The stated formula gives a calculated average molar mass of approximately 2,557.2 grams per mole. This is a formula-based calculation, not a batch measurement, and has not been reconciled with the supplied approximate mass of 2,554 daltons. Confirm the formula, structural form and mass convention against the manufacturer's specification before relying on either value.
The supplied registry number and formula are also listed in the product's Safety Data Sheet, which does not provide a molecular mass or confirm the synonym Da-74204. These catalogue details do not establish the identity, purity or complete formulation of the supplied batch. Refer to the manufacturer's specification and completed batch documentation for the exact material and any additional ingredients.
Chemical and formulation details are catalogue information, not new batch measurements. Check the exact material, chemical form, formulation and reported results against the manufacturer's specification and the certificate for the supplied batch.
The ULTIMATE specification
Additional purification
The ULTIMATE range specification concerns an additional preparative high-performance liquid chromatography purification stage beyond the Regular process. Confirm the documented process applicable to the selected product and batch.
More stringent endotoxin testing
The ULTIMATE range calls for a more stringent bacterial endotoxin testing specification. Refer to the product-specific batch records for the analytical method, acceptance criteria and reported results.
Confirm that the enhanced specification applies to this product and the supplied batch. The grade designation alone does not establish numerical purity, an endotoxin limit or sterility.
Product documentation
View the ULTIMATE Grade certificate for this product. The alternative-grade certificate is provided separately. The Material Safety Data Sheet is shared between Regular and ULTIMATE grades.
Grade-specific certificates
Certificate of Analysis
Select the certificate matching the product reference and grade on your label. Check that its batch number applies to the material supplied.
Shared by both grades
Material Safety Data Sheet
Consult the ADIPOTIDE (FTPP) safety document for information supporting laboratory handling, storage and disposal.
Documents open in a new tab. Match the product, grade and batch before relying on reported results. Contact Research Scientific for the applicable records if the document is unavailable or does not match your label.
Laboratory information
Presentation and quality documentation
The supplied product description identifies a lyophilised laboratory material in flip-top headspace vials. The description specifies milling and sieving for consistent handling. Where the supplied specification describes sterile material or packaging, confirm the relevant manufacturing and batch records; the container description alone does not establish a sterility result for its contents.
Review the applicable Certificate of Analysis for the tests performed, analytical methods and reported results. A catalogue specification is not a measurement of every supplied batch.
Laboratory preparation and storage
The supplied product information identifies bacteriostatic water containing 0.9% benzyl alcohol, or a suitable equivalent, as a laboratory reconstitution medium. Confirm compatibility with the exact material, full formulation and your laboratory's validated method.
Follow the product label and the current, formulation-specific Safety Data Sheet for handling, storage and disposal. Obtain product-specific stability information where required; no additional storage temperature or period after opening is established by this page.
Vial size options
The supplied catalogue lists the following options. Select the required option using the product controls; this list does not show current stock availability.
- 5 mg
- 10 mg
- 20 mg
- 50 mg
