5-AMINOLEVULINIC ACID HYDROCHLORIDE |
PRODUCT
IDENTIFICATION
|
CAS
NO. |
106-60-5 (Base),
5451-09-2 (Hydrochloride) |
|
EINECS
NO. |
226-679-5 |
FORMULA |
NH2CH2COCH2CH2COOH·HCl |
MOL
WT. |
167.59 |
H.S.
CODE |
2922.50.5000
|
TOXICITY |
|
SYNONYMS |
5-Amino-4-oxopentanoic acid hydrochloride; |
5-Amino-3-oxopentansaeure
(German); ácido 5-amino-3-oxopentanoico (Spanish);
Acide 5-amino-3-oxopentanoïque (French); gamma-Aminolevulinic acid hydrochloride;
delta-Aminolevulinic acid hydrochloride; Aminolevulinic acid hydrochloride;
5-Aminolevulinate hydrochloride; Levulan; Levulan Kerastick;
|
SMILES
|
NCC(CCC(O)=O)=O.Cl
|
CLASSIFICATION
|
Aminolevulinate,
Keto Acids, Dermatologic Agent, Hypoglycemic Agent,
Photosensitizing Agent, Radiation Sensitizing Agent,
Phototherapy.
|
PHYSICAL AND CHEMICAL PROPERTIES
|
PHYSICAL
STATE |
White
crystalline powder
|
MELTING POINT |
156 - 158 C
(Decomposes) |
BOILING
POINT |
|
SPECIFIC GRAVITY |
|
SOLUBILITY
IN WATER |
Soluble |
AUTOIGNITION |
|
pH |
|
VAPOR DENSITY |
5.78 |
NFPA RATINGS |
Health: 1; Flammability: 1; Reactivity: 0 |
REFRACTIVE
INDEX
|
|
FLASH
POINT |
|
STABILITY |
Stable under ordinary conditions. Hygroscopic. |
GENERAL
DESCRIPTION & APPLICATIONS
|
5-Aminolevulinic acid is an intermediate in heme biosynthesis in the body. Two
molecules of ALA are condensed to form porphobilinogen. It is the first step
compound in the porphyrin synthesis. Porphyrin is a class of cyclic
tetrapyrrolic ring structure compounds joined by four methene bridges (=C-)
through alpha-carbon atoms of four pyrroles. Porphyrins are water-soluble
biological pigments occuring widely in animal and plant tissues to take part in
important biological functions such as metal-binding cofactors in hemoglobins in
the blood of animals, chlorophyll in plants for photosynthesis, and certain
enzymes for cell respiration. Numerous types of porphyrins can be obtained
through the modification of a natural porphyrins and total synthesis. Not only
their chemical transformations through nucleophilic and electrophilic
substitution, substituent modification, reduction, oxidation but also thier
metalation and demetalation properties with iron, zinc, copper, nickel, and
cobalt give valuable biological applications in molecular biology,
fluoroimmunoassay, catalysts and new pharmaceutical developments. Wikipedia
Linking: http://en.wikipedia.org/wiki/5-Aminolevulinic_acid
|
SALES
SPECIFICATION |
APPEARANCE
|
White
crystalline powder
|
PURITY |
98.0%
min
|
WATER
|
0.5%
max
|
ASH
|
0.5%
max
|
HEAVY
METAL
|
20ppm
max
|
TRANSPORTATION |
PACKING |
|
HAZARD CLASS |
|
UN
NO. |
|
OTHER
INFORMATION |
FEMA Number: 2627 European Hazard
Symbols: , Risk Phrases: 36/36/38-66,
Safety Phrases: 26-36/37 |
GENERAL
DESCRIPTION OF PHOTOSENSITIZING AGENTS
|
Photosensitizing agents such as Hematoporphyrin D are pharmacologically inactive
but when excited by visible light or a specific wavelength concentrate
selectively in metabolically active diseased tissue and are converted to active
metabolite to produce a beneficial reaction affecting the tissue by the
production of cytotoxic free radicals. Photosensitizers are used in the
photodynamic therapy. Photosensitizers are administered topically or
systemically and have been used therapeutically to treat psoriasis, acne and
various types of neoplasms. Photosensitizing agents include:
Photosensitizing Agent |
CAS
RN
|
Acetophenone
|
98-86-2 |
Afloqualone |
56287-74-2 |
alpha-Terthienyl
|
1081-34-1 |
Aluminum phthalocyanine
disulfonate |
68637-19-4 |
Aminomethyltrioxsalen
|
64358-50-5 |
Bacteriochlorin A |
103428-20-2 |
Benzophenone
|
119-61-9 |
Benzoporphyrin D |
113719-89-4 |
Bergamot oil
|
8007-75-8 |
Bergaptol
|
486-60-2 |
Bis(dimethylthexylsiloxy)silicon
2,3-naphthalocyanine |
153454-02-5 |
Bis(tri-n-hexylsiloxy)(2,3-naphthalocyaninato)silicon
|
92396-88-8 |
Cadmium texaphyrin
|
115677-78-6 |
Carprofen
|
52263-47-5 |
Chlorin P6
|
22006-68-4 |
Chloroaluminum
tetrasulfophthalocyanine |
104469-80-9 |
Chloroaluminum-1,11,15,25-tetramethyl-tetrapyrido-porphyrazine |
150437-07-3 |
Chloroaluminum-1,8,15,22-tetramethyl-tetrapyrido-porphyrazine |
150437-06-2 |
Copper benzochlorin
|
145582-83-8 |
Ficusin
|
66-97-7 |
Fullerene C60
|
99685-96-8 |
Gilvocarcin V |
77879-90-4 |
Hematoporphyrin
dicyclohexanyl ether |
119052-80-1 |
Hematoporphyrin D |
68335-15-9 |
Hematoporphyrin dihexyl
ether |
111922-13-5 |
Hematoporphyrin diphenyl
ether |
119052-81-2 |
Hypocrellin A
|
77029-83-5 |
Hypocrellin B
|
123940-54-5 |
Lomefloxacin |
98079-51-7 |
Lumin
|
80893-93-2 |
Lysyl chlorin P6
|
140395-23-9 |
Merocyanine 540 |
58823-12-4 |
meso-Chlorin e6
monoethylene diamine |
147740-90-7 |
Methoxsalen |
298-81-7 |
Monoaspartyl chlorin E6
|
110230-98-3 |
Nitrogen dioxide
|
10102-44-0 |
Ozone
|
10028-15-6 |
Polymyxin B nonapeptide
|
86408-36-8 |
Protoporphyrin IX
|
553-12-8 |
Pyrido(3,4-c)-7-methylpsoralen
|
85878-63-3 |
Riboflavin |
83-88-5 |
Silicon phthalocyanine
|
135719-28-7 |
Talaporfin sodium
|
220201-34-3 |
Tetra(4-N-methylpyridyl)porphine
|
38673-65-3 |
Tiaprofenic acid |
33005-95-7 |
Tin etiopurpurin
|
113471-15-1 |
Tin(IV) chlorin E6
|
128835-29-0 |
Trioxsalen |
3902-71-4 |
Verdin
|
12713-07-4 |
Verteporfin |
129497-78-5 |
Victoria blue BO |
2390-60-5 |
Zinc
tetrabenzylpyridoporphyrin |
146190-75-2 |
Zn(II)-Phthalocyanine
|
14320-04-8 |
1,6-Diphenyl-3-hexene-1,5-diyne |
27370-85-0 |
1,9-Dimethylmethylene
blue |
23481-50-7 |
1-Pyrenemethyl-23,24-bisnor-5-cholen-22-oate-3beta-yl
oleate |
72535-39-8 |
2-(1-Hexyloxyethyl)-2-devinyl
pyropheophorbide-a |
149402-51-7 |
2,3-Naphthalocyanine
|
23627-89-6 |
2,4-Bis(1-decyloxyethyl)-Ga(III)-1,3,5,8-tetramethylporphyrin-6,
7-dipropionyl
diaspartic acid |
135099-39-7 |
2,6-Dimethyl-9-methoxy-4H-pyrrolo(3,2,1-ij)quinolin-4-one
|
131195-83-0 |
3,7,12,17-Tetramethyl-21H,23H-porphine-2,18-dipropanoic acid |
448-65-7 |
4-Methoxycinnamate methyl
ester |
832-01-9 |
5-(N-Hexadecanoyl)aminoeosin
|
114586-25-3 |
5,10,15,20-Tetra(4-hydroxyphenyl)porphyrin
|
51094-17-8 |
5-Aminolevulinic
acid |
106-60-5 |
6-Methylthionecoumarin
|
60257-28-5 |
8-Methoxythionepsoralen
|
72142-97-3 |
|
|
|