(3-(3-aminopropanamido)propanoyl)-L-histidine CAS CATO-C3D-4642

Purity >95%In StockPharmaceutical Standards
CAS No.CATO-C3D-4642
Molecular FormulaC12H19N5O4
Molecular Weight297.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-(3-aminopropanamido)propanoyl)-L-histidine CAS CATO-C3D-4642 chemical structure

Description

As a certified reference material (CRM), (3-(3-aminopropanamido)propanoyl)-L-histidine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

(3-(3-aminopropanamido)propanoyl)-L-histidine (CAS CATO-C3D-4642) is a high-purity analytical reference standard with the molecular formula C12H19N5O4 and a molecular weight of 297.31 g/mol.

Structurally, (3-(3-aminopropanamido)propanoyl)-L-histidine (C12H19N5O4) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 297.31 g/mol, it falls into the medium-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC12H19N5O4
Molecular Weight297.31 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity>95%
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms5

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