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SUMATRIPTAN | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 103628-46-2 | |
EINECS NO. | ||
FORMULA | C13H19N3O2S | |
MOL WT. | 281.37 | |
H.S. CODE |
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TOXICITY |
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SYNONYMS | Imigran; Imitrex; | |
3-[2-(Dimethylamino)ethyl]-N-methyl-1H-indole-5-methanesulfonamide;
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SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | White to off-white crystalline powder | |
MELTING POINT | 164 - 165 C | |
BOILING POINT | ||
SPECIFIC GRAVITY | ||
SOLUBILITY IN WATER | ||
pH | ||
VAPOR DENSITY |
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AUTOIGNITION |
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NFPA RATINGS |
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REFRACTIVE INDEX |
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FLASH POINT |
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STABILITY | Stable under ordinary conditions. | |
APPLICATIONS |
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Sumatriptan
[su(lfon)am(ide) triptan] is a selective serotonin antagonist used in the treatment of
migraine headache. It is a white to off-white powder; soluble in water and in
saline. Its chemical designation is 3-[2-(Dimethylamino)ethyl]- N-methyl- indole-
5-methanesulfonamide. Its succinate
is administered subcutaneously and orally. |
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SALES SPECIFICATION | ||
APPEARANCE |
White to off-white crystalline powder | |
IDENTIFICATION |
Complies |
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ASSAY (HPLC) |
98.5% min | |
MELTING POINT | 164 - 165 C | |
LOSS ON DRYING |
0.5% max |
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HEAVY METALS |
20ppm max |
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RESIDUE ON IGNITION |
0.1% max |
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RELATED MATERIAL | 1.5% max | |
TRANSPORTATION | ||
PACKING | 10kgs in tin can | |
HAZARD CLASS | ||
UN NO. | ||
GENERAL DESCRIPTION OF TYRAMINE & TRYPTAMINE |
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Tyramine [4-(2-Aminoethyl)phenol] is a monoamine compound of 4-hydroxy phenethylamine. It is derived from tyrosine, an amino acid (protein building block) that is the precursor of norepinephrine. It, through its effect on neurotransmitters, may affect several health conditions, including Parkinson's disease, depression, alcohol withdrawal support, and Phenylketonuria. (PKU). Tyramine is naturally found in plant and animal tissues, certain cheeses and ergot or produced synthetically. It is metabolized by monoamine oxidase. Tyramine or its derivatives can be used in pharmaceutical industry such as:
Tryptamine [3-(2-Aminoethyl)indole] is a biologically important monoamine compound derived by the decarboxylation of tryptophan, indole side chain amino acid. In addition to its function to build the structure of protein, tryptophan is a precursor for neurotransmitter and neurohormone. Tryptamine (biological monoamine) effects vasoconstriction by causing the release of norepinephrine at postganglionic nerve endings. Several mental disorders and health conditions are explained as due to either an excess or deficiency of monoamines. There are many natural tryptamines in both animal and plant as well as synthetics modified by chemical constituents and substituted at appropriate positions in the motif. Common tryptamine class compounds include;
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