Frag (17-23) TB-500 10mg – Lyophilized Peptide Powder

Global Peptides Lab presents Frag (17-23) TB-500 10mg, a lyophilized peptide powder supplied in a sealed vial for laboratory research purposes. This product listing provides essential information about the product’s presentation, container size, physical form, and available batch-testing results.

The peptide is supplied as a dry powder rather than a reconstituted solution. This distinction is important for research inventory management, product identification, and laboratory documentation. Each vial has a nominal product quantity of 10mg and is packaged in a 3ml vial with a sealed flip-top closure.

Researchers and laboratory purchasers can use the specifications on this page to identify the listed product and review the available quality-control information before making a purchasing decision.

Product Specifications

The following details describe the product as supplied by Global Peptides Lab.

• Product name: Frag (17-23) TB-500
• Listed quantity: 10mg
• Product category: Research peptide
• Physical form: Lyophilized powder
• Container type: Vial
• Vial capacity: 3ml
• Closure: Sealed flip-top
• Reconstitution status: Not reconstituted
• Available quality-control checks: Purity, weight, and endotoxins (LPS)

The 10mg designation represents the nominal product quantity used in the listing. The actual measured weight reported for the supplied batch is provided separately in the test results section below.

Understanding Lyophilized Peptide Powder

Lyophilization, commonly called freeze-drying, is a process used to remove water from a material under controlled conditions. It is used in various laboratory and pharmaceutical settings to produce dry preparations.

For peptide research materials, the lyophilized form is a product presentation rather than a guarantee of purity, stability, or suitability for a particular experiment. Those characteristics depend on the material, manufacturing process, testing methods, packaging, and storage conditions.

Frag (17-23) TB-500 10mg is supplied as a dry powder and is not reconstituted. The product should therefore be identified and handled according to its documented research specifications and any accompanying laboratory instructions. Do not assume that the vial contains a ready-to-use liquid solution.

The 3ml figure refers to the vial’s stated capacity, not the volume of liquid inside the container. Because the product is supplied as powder, vial capacity should not be confused with product quantity.

Batch Testing and Quality-Control Information

Quality-control testing provides information about specific characteristics of a material. The results available for this product include a reported purity percentage, measured weight, and endotoxin screening outcome.

Reported test results

The supplied batch-testing record contains the following information:

Test or identifier	Reported result
Date tested	May 12, 2026
Purity	99.948%
Measured weight	11.06mg
Endotoxins (LPS)	Pass
Batch number	FTB06260510E

These figures are reported from the product information provided for this listing. Buyers should consult the corresponding laboratory report or certificate of analysis, where available, for details about the testing laboratory, analytical methods, acceptance criteria, and sample identification.

What does the purity result mean?

The reported purity result of 99.948% describes the value stated in the supplied test record. The meaning and reliability of a purity percentage depend on the analytical method, sample preparation, and reporting convention used by the testing laboratory.

A high reported purity result should not automatically be interpreted as proof of overall product quality, biological activity, sterility, or suitability for human use. Those are separate characteristics that require appropriate evidence.

What does the measured weight mean?

The batch record reports a measured weight of 11.06mg, while the product is listed as 10mg. These are separate figures and should be presented transparently.

The available information does not establish whether the measured weight represents net peptide content, total powder weight, or another measurement convention. Refer to the original test report for clarification before drawing conclusions about the difference.

What does an endotoxin test check?

Endotoxins, also known as lipopolysaccharides (LPS), are components associated with the outer membrane of certain bacteria. Endotoxin testing evaluates a sample for these substances using a specified analytical method.

The supplied record states that the endotoxin result is “Pass.” However, the testing method, numerical result, and acceptance limit have not been provided here. A pass result should not be treated as proof of sterility or as confirmation that a product is safe for injection.

Packaging and Product Presentation

This product is supplied in a sealed, flip-top vial with a stated capacity of 3ml. Its lyophilized powder form distinguishes it from products supplied as pre-prepared liquid solutions.

The packaging information helps buyers identify the container and understand how the product is presented. The sealed closure is a packaging feature and, by itself, does not establish sterility, tamper-evident certification, or compliance with any particular pharmaceutical standard.

Before purchasing, compare the listed quantity, product identity, batch number, and accompanying documentation. If the laboratory report is available, check that its batch identifier matches the product being supplied.

Storage and Handling Information

Follow the manufacturer’s documented storage conditions and any instructions supplied with the product. Specific temperature limits, light-protection requirements, shelf life, and post-opening stability should not be assumed when they have not been documented.

Maintain appropriate laboratory inventory records, retain the product identification and batch number, and follow applicable laboratory safety procedures. Any handling or disposal should comply with relevant institutional requirements and local regulations.

No reconstitution instructions, administration guidance, or claims about human use are provided in this listing. The product is intended for laboratory research purposes only and is not presented as a medicine or as a product for self-administration.

Why Review Product Documentation Before Ordering?

Clear product documentation supports informed purchasing and helps laboratory buyers distinguish between nominal product specifications and measured test results.

When reviewing this peptide listing, consider the following:

• Confirm the product name and nominal quantity.
• Review the stated physical form and vial capacity.
• Check the available purity and endotoxin results.
• Compare the reported batch number with the accompanying documentation.
• Ask for the relevant analytical report if you need further details about test methods or acceptance criteria.
• Verify applicable research-use restrictions before ordering.

Global Peptides Lab aims to present product specifications in a clear, accessible format so that purchasers can review the available information before proceeding.

Frequently Asked Questions

What is Frag (17-23) TB-500 10mg?

It is the name used for this listed research peptide product, supplied as a nominal 10mg quantity of lyophilized powder in a sealed 3ml vial. The exact identity and characterization should be verified using appropriate product documentation.

Is this product supplied as a liquid?

No. The listed product is supplied as lyophilized powder and is not reconstituted.

What is the reported purity?

The supplied batch-testing information reports a purity of 99.948%, dated May 12, 2026. Refer to the original laboratory report for the method and interpretation of this result.

What is the measured weight?

The reported measured weight is 11.06mg. The basis of this measurement should be confirmed using the original report because it differs from the nominal 10mg product designation.

Has the product been tested for endotoxins?

The supplied record lists the endotoxin (LPS) result as “Pass.” The testing method and acceptance threshold should be confirmed from the original laboratory documentation. This result alone does not demonstrate sterility.

What is the batch number?

The batch number supplied for this listing is FTB06260510E. Use this identifier when checking the corresponding test documentation.

Is the product intended for human use?

No. This listing is for laboratory research purposes only and is not intended for human or veterinary use, diagnosis, treatment, or prevention of disease.

Order Research Peptides from Global Peptides Lab

Before placing an order, review the product specifications and available testing information to make sure the listed material meets your documentation requirements. If you require additional information about the batch, testing methods, or product identity, request the relevant supporting documentation from Global Peptides Lab.

Frag (17-23) TB-500 10mg is listed with a nominal 10mg quantity, lyophilized powder presentation, sealed 3ml flip-top vial, and batch-testing information for purity, weight, and endotoxins. Review the available documentation carefully and follow all applicable laboratory research requirements.

Research use only. Not for human or veterinary use.