???
|
|
??? ??
- ???
- 160-162 °C(lit.)
- ?? ?
- 175-181 °C8 mm Hg(lit.)
- ??
- 1.0630 (rough estimate)
- ???
- 1.5849 (estimate)
- FEMA
- 4215 | TYRAMINE
- ???
- 165°C
- ?? ??
- 2-8°C
- ???
- DMSO(?? ???), ???(?? ???)
- ??? ??
- ??
- ?? ?? (pKa)
- 9.74(at 25℃)
- ??
- ??? ????? ????? ?? ????, ?? ? ???? ? ??
- ??
- 100.00%??. ?? ?? ?? ??? ?? ??? ?? ??
- ?? ??
- ??? ??
- ???? ??
- synthetic
- ???
- 1g/95mL(15℃)
- Merck
- 14,9835
- JECFA Number
- 1590
- BRN
- 1099914
- ???
- ????. ??, ????? ???? ????.
- LogP
- 1.38
- CAS ??????
- 51-67-2(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
??? ?? | Xi | ||
---|---|---|---|
?? ???? ?? | 36/37/38 | ||
????? | 26-36-37/39 | ||
WGK ?? | 3 | ||
RTECS ?? | SJ5950000 | ||
F ?????? | 10-23 | ||
HS ?? | 29214990 | ||
?? ?? ??? | 51-67-2(Hazardous Substances Data) | ||
?? | LD50 intracervical in mouse: 30mg/kg |
??? C??? ??, ??, ??
??
A decarboxylation product of tyrosine found in various fermentation products, including cheeses and some wines. It causes sympathomimetic effects by acting as an indirect agonist, causing the release of endogenous catecholamines. Because it is metabolized principally by monoamine oxidase, patients taking monoamine oxidase inhibitors may have a hypertensive crisis if they ingest foods containing significant amounts of tyramine.??? ??
white to light beige solid??
Reported found in sauerkraut and soy sauce.??
tyramine is uses as pharmaceutical intermediates.??
ChEBI: A primary amino compound obtained by formal decarboxylation of the amino acid tyrosine.Purification Methods
Crystallise tyramine from *benzene or EtOH. [Beilstein 13 IV 1788.]??? ?? ?? ? ???
???
?? ??
??? ?? ??
???( 618)?? ??
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