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Certifikat analize: DSIP, serija ATDSP-05-2505-01

DSIP, serija ATDSP-05-2505-01, testiral neodvisni laboratorij Analyton Labs, certifikat AN-2026-00003, izdan 22. september 2026: čistost 99.88 ± 0.20 % z metodo RP-HPLC, 4.88 mg peptida na vialo, trifluoroacetat < 20 ppm, bakterijski endotoksini < 0.05 EU/mg, skupaj 21 določitev.

Izdelek
DSIP
Serija
ATDSP-05-2505-01
Številka certifikata
AN-2026-00003
Laboratorij
Analyton Labs
Datum izdaje
Vzorec
DSIP, lyophilised powder, vial labelled 5 mg

Pregled rezultatov, 21 določitev

Metode in rezultati so navedeni v angleščini, natanko tako, kot jih je zabeležil laboratorij.

Pregled rezultatov, 21 določitev
Določitev Metoda Rezultat Specifikacija
Appearance Visual White to off-white powder White to off-white powder
Purity RP-HPLC, C18, 214 nm (280 nm control trace), area % 99.88 ± 0.20 % (k = 2) >= 98.0 %
Related substances RP-HPLC, 214 nm; LOD 0.01 %, LOQ 0.03 %, reporting threshold 0.05 % Largest single impurity 0.07 % at RRT 0.96 (± 0.03 %); total impurities 0.12 %, i.e. 0.006 mg per vial Single <= 1.0 %, total <= 2.0 %
Impurity profile RP-HPLC with LC-HRMS assignment RRT 0.90, 0.05 %, +16/+32 Da (Trp oxidation: kynurenine, hydroxytryptophan); RRT 0.96, 0.07 %, same mass (isoAsp) Peaks above 0.05 % reported (ICH Q3B)
Net peptide content Assay 93.88 ± 1.2 % w/w (k = 2)
Fill weight Gravimetric 5.20 ± 0.05 mg Labelled 5 mg
Peptide per vial Calculated from fill weight and net peptide content 4.88 mg per vial labelled 5 mg, i.e. 97.6 % of label 95 to 105 % of label
Vial-to-vial consistency Gravimetric, two vials of the batch 5.20 and 5.33 mg, difference 2.5 %; purity of both within 0.1 % <= 5 %
Counter-ion content Ion chromatography Sodium 0.90 % w/w (± 0.05 %), i.e. 0.05 mg per vial; acetate < 0.05 %
Trifluoroacetate Ion chromatography, LOQ 20 ppm < 20 ppm; acetate, chloride and phosphate below LOQ <= 1000 ppm
Water content Coulometric Karl Fischer, USP <921> 4.80 ± 0.24 % w/w (k = 2), i.e. 0.25 mg per vial <= 8.0 %
Mass balance Peptide + counter-ion + water 93.88 + 0.90 + 4.80 = 99.58 % (± 1.3 %) Close to 100 %
pH Potentiometric, 5 mg/ml in water 5.2 4.4 to 6.0
Solubility Visual, 5 mg/ml and 1 mg/ml >= 5 mg/ml in water and in bacteriostatic water; clear, colourless to faintly yellow, free of particles within 30 s Clear solution
Bacterial endotoxins Kinetic chromogenic LAL, USP <85> < 0.05 EU/mg (< 0.26 EU per vial) <= 10 EU/mg
Sterility Membrane filtration, USP <71>; fluid thioglycollate 30 to 35 °C and soya bean casein digest 20 to 25 °C No growth after 14 days, 2 vials No growth
Microbial enumeration Plate method, USP <61> and <62> TAMC < 10 CFU/g, TYMC < 10 CFU/g; E. coli, Salmonella, S. aureus and P. aeruginosa absent in 1 g TAMC <= 1000 CFU/g, TYMC <= 100 CFU/g, specified organisms absent
Residual solvents Headspace GC, USP <467> Acetonitrile 45 ppm; N,N-dimethylformamide, methanol, dichloromethane, diethyl ether, diisopropyl ether and piperidine each < 10 ppm (LOQ 10 ppm) ICH Q3C: acetonitrile <= 410, DMF <= 880, methanol <= 3000, dichloromethane <= 600, ethers <= 5000 ppm
Elemental impurities ICP-MS after microwave digestion (HNO3/H2O2), USP <233> Cd, Pb, As, Hg < 0.05 µg/g; Co, V, Ni < 0.10 µg/g, all below LOQ ICH Q3D(R2) Class 1 and 2A, parenteral PDE
Chiral purity (D-amino acids) Acid hydrolysis (6 M DCl in D2O, 110 °C, 24 h), Marfey's derivatisation (FDAA), LC-MS D-Asp 0.12 %, D-Ser 0.08 %, D-Glu 0.05 %, others < 0.05 %; Gly achiral; sum of D-forms 0.29 % Each D-amino acid <= 0.2 %, sum of D-forms <= 0.5 %
Compound screening LC-HRMS full scan, m/z 100 to 2000, against library: fentanyl and analogues, Epithalon, Selank, Semax, protected intermediates (tBu, Boc, Trt, Pbf, Fmoc), free amino acids None detected above 0.05 % area No foreign compound above 0.05 % area

SHA-256 datoteke: f4cab91a00e44da3c648e513a70550bbf1624c5d323606e4b0313027e7e17782

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