The long term stability of this product at room temperature has not been determined. However, the item is shipped at ambient temperature and is stable for short periods of time. Note that shipping routes are configured to minimize transit time.
Select a Size
| Size/SKU | Availability | Price |
|---|---|---|
6.53 mg | Please contact Customer Service for Availability | 5 870,00 kr |
About This Item
grade
pharmaceutical primary standard
agency
USP
API family
gonadorelin
form
powder
manufacturer/tradename
USP
application(s)
USP Biologics
pharmaceutical (small molecule)
format
neat
storage temp.
−20°C
SMILES string
[nH]1cnc(c1)C[C@H](NC(=O)[C@H]6NC(=O)CC6)C(=O)N[C@@H](Cc4c5c([nH]c4)cccc5)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc3ccc(cc3)O)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N2[C@@H](CCC2)C(=O)NCC(=O)N
InChI
1S/C55H75N17O13/c1-29(2)19-38(49(80)67-37(9-5-17-60-55(57)58)54(85)72-18-6-10-43(72)53(84)62-25-44(56)75)66-46(77)26-63-47(78)39(20-30-11-13-33(74)14-12-30)68-52(83)42(27-73)71-50(81)40(21-31-23-61-35-8-4-3-7-34(31)35)69-51(82)41(22-32-24-59-28-64-32)70-48(79)36-15-16-45(76)65-36/h3-4,7-8,11-14,23-24,28-29,36-43,61,73-74H,5-6,9-10,15-22,25-27H2,1-2H3,(H2,56,75)(H,59,64)(H,62,84)(H,63,78)(H,65,76)(H,66,77)(H,67,80)(H,68,83)(H,69,82)(H,70,79)(H,71,81)(H4,57,58,60)/t36-,37-,38-,39-,40-,41-,42-,43-/m0/s1
InChI key
XLXSAKCOAKORKW-AQJXLSMYSA-N
General description
Gonadorelin hydrochloride is a synthetic form of gonadotropin-releasing hormone (GnRH), used diagnostically and therapeutically to assess pituitary function. The USP standard supports identity, potency, and purity testing in gonadorelin drug substances.
The USP biologics peptides category encompasses a diverse range of therapeutic peptides that are essential in managing various medical conditions. These peptides, typically consisting of amino acid sequences of 40 residues or less, are critical for the development of high-quality medicines. The USP provides comprehensive standards, reference materials, and analytical procedures to ensure the identity, quality, purity, and consistency of peptide therapeutics throughout their lifecycle.
The United States Pharmacopeia (USP) provides quality standards for biologics to ensure their safety, efficacy, and quality throughout the manufacturing process. These standards assist manufacturers in adhering to regulatory requirements and help safeguard public health by reducing risks associated with biologics.
Application
Also used to prepare standard, system suitability, and standard stock solution during the assay, and impurity analysis of Gonadorelin Hydrochloride and Gonadorelin for Injection.
Analysis Note
Other Notes
1 of 1
This Item | |||
|---|---|---|---|
| description United States Pharmacopeia (USP) Reference Standard | description United States Pharmacopeia (USP) Reference Standard | description United States Pharmacopeia (USP) Reference Standard | description European Pharmacopoeia (EP) Reference Standard |
| manufacturer/tradename USP | manufacturer/tradename USP | manufacturer/tradename USP | manufacturer/tradename EDQM |
| grade pharmaceutical primary standard | grade pharmaceutical primary standard | grade pharmaceutical primary standard | grade pharmaceutical primary standard |
| application(s) USP Biologics | application(s) USP Biologics | application(s) pharmaceutical | application(s) pharmaceutical (small molecule) |
| format neat | format neat | format - | format neat |
| form powder | form solid | form powder | form - |
| API family gonadorelin | API family gonadotropin | API family fingolimod | API family leuprorelin |
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
signalword
Warning
hcodes
Hazard Classifications
Repr. 2 - STOT RE 2
target_organs
Endocrine system
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What is the stability of Gonadorelin HCL at room temperature? When is it deemed unacceptable to use if stored at room temperature?
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