- 5-Aminolevulinic acid
- 5-Aminolevulinic acid benzyl ester hydrochloride
- 5-Aminolevulinic acid hexyl ester hydrochloride
- 5-Aminolevulinic acid hydrochloride
- 5-Aminolevulinic acid hydrochloride
- 5-Aminolevulinic acid methyl ester hydrochloride
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Cas Database |
| Name |
5-Aminolevulinic acid methyl ester hydrochloride |
EINECS | 279-151-1 |
| CAS No. | 79416-27-6 | Density | N/A |
| PSA | 69.39000 | LogP | 0.96970 |
| Solubility | very faint turbidity | Melting Point |
119-121° |
| Formula | C6H11NO3.HCl | Boiling Point | 228°C at 760 mmHg |
| Molecular Weight | 181.619 | Flash Point | 99.5°C |
| Transport Information | N/A | Appearance | N/A |
| Safety | 26-36 | Risk Codes | 36/37/38 |
| Molecular Structure |
|
Hazard Symbols |
 Xi
|
| Synonyms |
Metvix;P 1202;d-Aminolevulinic acid methyl ester hydrochloride;Pentanoicacid, 5-amino-4-oxo-, methyl ester, hydrochloride (9CI);5-Amino-4-oxopentanoicacid methyl ester hydrochloride;Methyl 5-amino-4-oxopentanoate hydrochloride;Methyl5-aminolevulinate hydrochloride;Methyl ALA ester hydrochloride;Methylaminolevulinate hydrochloride; |
Article Data | 7 |
5-Aminolevulinic acid methyl ester hydrochloride Synthetic route
| Conditions | Yield |
|---|---|
| With thionyl chloride at 20℃; for 30h; | 86.3% |
| With thionyl chloride at 20℃; for 48h; | 81% |
| With thionyl chloride at 0 - 20℃; | |
| With thionyl chloride |
| Conditions | Yield |
|---|---|
| With thionyl chloride at 60℃; for 5h; |
- 53856-93-2
methyl 5-bromo-4-oxopentanoate
- 79416-27-6
methyl aminolevulinate
| Conditions | Yield |
|---|---|
| Multi-step reaction with 3 steps 1: 1.) K2CO3 / 1.) DMFA, 20 deg C, 20 min, 2.) 72 h, 3.) water, 20 deg C, 24 h 2: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 3: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
- 109258-71-1
methyl 5-(1,3-dioxoisoindolin-2-yl)-4-oxopentanoate
- 79416-27-6
methyl aminolevulinate
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 2: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
- 123-76-2
levulinic acid
- 79416-27-6
methyl aminolevulinate
| Conditions | Yield |
|---|---|
| Multi-step reaction with 4 steps 1: 10.7 g / Br2, urea / 48 h / 20 °C 2: 1.) K2CO3 / 1.) DMFA, 20 deg C, 20 min, 2.) 72 h, 3.) water, 20 deg C, 24 h 3: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 4: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
- 114681-18-4
2,2-dimethyl-4,6-dioxo-5-(3-phthalimido-2-oxopropyl)-1,3-dioxane
- 79416-27-6
methyl aminolevulinate
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 2: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
- 5451-09-2
5-aminolevulinic acid hydrochloride
- 79416-27-6
methyl aminolevulinate
| Conditions | Yield |
|---|---|
| With hydrogenchloride In methanol | |
| With hydrogenchloride In methanol |
- 79416-27-6
methyl aminolevulinate
- 203866-13-1
(2S,4S)-1-(tert-butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid
- 871979-17-8
5-[(1-tert-butoxycarbonyl-(4S)-fluoro-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
| Conditions | Yield |
|---|---|
| With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
- 79416-27-6
methyl aminolevulinate
- 83624-01-5
(2S,4R)-1-(tert-butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylic acid
- 871979-27-0
5-[(1-tert-butoxycarbonyl-(4R)-methoxy-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
| Conditions | Yield |
|---|---|
| With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
- 15761-39-4
1-(tert-butoxycarbonyl)-L-proline
- 79416-27-6
methyl aminolevulinate
- 871979-33-8
N-(N-tert-butoxycarbonyl-L-prolyl)-5-aminolaevulinic acid methyl ester
| Conditions | Yield |
|---|---|
| With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
5-Aminolevulinic acid methyl ester hydrochloride Chemical Properties
Molecular Structure:
.gif)
Molecular Formula: C6H12ClNO3
Molecular Weight: 181.6174
IUPAC Name: Methyl 5-amino-4-oxopentanoate hydrochloride
Synonyms of 5-Aminolevulinic acid methyl ester hydrochloride (CAS NO.79416-27-6): Methyl aminolevulinate hydrochloride [USAN] ; EINECS 279-151-1 ; Methyl 5-amino-4-oxopentanoate hydrochloride ; Methyl aminolevulinate HCl ; Methyl aminolevulinate hydrochloride ; Metvix PDT ; Metvixia ; P-1202 ; Pentanoic acid, 5-amino-4-oxo-, methyl ester, hydrochloride ; UNII-7S73606O1A
CAS NO: 79416-27-6
Product Categories: Fatty & Aliphatic Acids, Esters, Alcohols & Derivatives
Flash Point: 99.5 °C
Enthalpy of Vaporization: 46.45 kJ/mol
Boiling Point: 228 °C at 760 mmHg
Vapour Pressure of 5-Aminolevulinic acid methyl ester hydrochloride (CAS NO.79416-27-6): 0.0754 mmHg at 25°C
5-Aminolevulinic acid methyl ester hydrochloride Safety Profile
of 5-Aminolevulinic acid methyl ester hydrochloride (CAS NO.79416-27-6)Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-36
WGK Germany: 3
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