Identification | Back Directory | [Name]
5-Aminolevulinic acid hexyl ester hydrochloride | [CAS]
140898-91-5 | [Synonyms]
Hexvix P 1206 Hexaminolevulinate HCl ALA HEXYL ESTER HYDROCHLORIDE AMINOLEVULINC ACID HEXYL ESTER Hexaminolevulite hydrochloride HexaMinolevulinate hydrochloride Hexyl 5-aMinolevulinate hydrochloride N-HEXYL 5-AMINOLEVULINATE HYDROCHLORIDE Hexyl 5-amino-4-oxopentanoate hydrochloride AMINOLEVULINIC ACID HEXYL ESTER HYDROCHLORIDE Hexaminolevulinate hydrochloride >=98% (HPLC) Hex-1-yl 5-amino-4-oxopentanoate hydrochloride 5-AMINOLEVULINIC ACID HEXYL ESTER HYDROCHLORIDE DELTA-AMINOLEVULINIC ACID HEXYL ESTER HYDROCHLORIDE 5-AMINO-4-OXOPENTANOIC ACID HEXYL ESTER HYDROCHLORIDE 3-AMinoacetylpropionic acid hexyl ester hydrochloride Pentanoic acid, 5-amino-4-oxo-, hexyl ester, hydrochloride Pentanoic acid, 5-aMino-4-oxo-, hexyl ester, hydrochloride (9CI) Hex-1-yl 5-aminolevulinate hydrochloride, Hex-1-yl 5-amino-4-oxovalerate hydrochloride HEXYL 5-AMINOLEVULINATE HYDROCHLORIDE; P-1206; 5-AMINOLEVULINIC ACID HEXYL ESTER HYDROCHLORIDE Hexyl 5-AMinolevulinate hydrochloride,3-AMinoacetylpropionic acid hexyl ester hydrochloride,Hexyl 5-aMino-4-oxopentanoate Hexyl 5-AMinolevulinate hydrochloride | [Molecular Formula]
C11H22ClNO3 | [MDL Number]
MFCD03695491 | [MOL File]
140898-91-5.mol | [Molecular Weight]
251.75 |
Chemical Properties | Back Directory | [Melting point ]
94° | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
DMSO:41.0(Max Conc. mg/mL);162.86(Max Conc. mM) | [form ]
A solid | [color ]
White to off-white | [Water Solubility ]
H2O: 20mg/mL, clear | [Sensitive ]
Light Sensitive/Hygroscopic | [InChI]
InChI=1S/C11H21NO3.ClH/c1-2-3-4-5-8-15-11(14)7-6-10(13)9-12;/h2-9,12H2,1H3;1H | [InChIKey]
LZYXPFZBAZTOCH-UHFFFAOYSA-N | [SMILES]
C(=O)(OCCCCCC)CCC(=O)CN.Cl |
Hazard Information | Back Directory | [Uses]
Diagnostic agent for the diagnosis of bladder cancer. | [Biological Activity]
Hexaminolevulinate (HAL) hydrochloride is a hexyl ester of 5-Aminolevulinic acid (ALA)a precursor to porphyrins including the photosensitizer protoporphyrin IX (PPIX). Hexaminolevulinate is more lipophilic than ALAand is 50–100 times more efficient than ALA at inducing PpIXwhich accumulates preferentially in neoplastic cells. Hexaminolevulinate administration followed by light activation has been used for fluorescence cystoscopy to enhance detection of bladder cancerin particular carcinoma in situ (CIS). Hexaminolevulinate is also being studied for use in cancer photodynamic therapy. Hexaminolevulinate followed by irradiation produced DNA oxidative damage and apoptosis. |
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