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Hexaminolevulinate hydrochloride

SIGMA/SML1637 - ≥98% (HPLC)

Synonym: 5-Aminolevulinic acid hexyl ester HAL hydrochloride; 5-Aminolevulinic acid hexyl ester hydrochloride; HAL; Hexvix; Hexyl 5-aminolevulinate hydrochloride; P 1206; n-Hexyl 5-aminolevulinate hydrochloride

CAS Number: 140898-91-5
Empirical Formula (Hill Notation): C11H21NO3 · HCl
Molecular Weight: 251.75
MDL Number: MFCD03695491
Linear Formula: C11H21NO3 · HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML1637-10MG 10 mg
$108.00
1/EA
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45-SML1637-50MG 50 mg
$435.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
InChI 1S/C11H21NO3.ClH/c1-2-3-4-5-8-15-11(14)7-6-10(13)9-12;/h2-9,12H2,1H3;1H
InChI key LZYXPFZBAZTOCH-UHFFFAOYSA-N
Quality Level 100 
SMILES string CCCCCCOC(CCC(CN)=O)=O.[H]Cl
solubility H2O: 20 mg/mL, clear
storage condition desiccated
storage temp. room temp
Biochem/physiol Actions: 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 ALA, and is 50–100 times more efficient than ALA at inducing PpIX, which accumulates preferentially in neoplastic cells. Hexaminolevulinate administration followed by light activation has been used for fluorescence cystoscopy to enhance detection of bladder cancer, in 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.
Packaging: 10, 50 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Purity ≥98% (HPLC)
Storage Temp. room temp
UNSPSC 12352200

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