Histamine phosphate
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Histamine phosphate
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CAS No:
51-74-1
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Formula:
C5H12N3O4P
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Chemical Name:
Histamine phosphate
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Synonyms:
HISTAMINEPHOSPHATE,USP;2-(4-Imidazolyl)ethylamine diphosphate salt, 2-(4-Imidazolyl)ethylamine monohydrate diphosphate salt, Histamine monohydrate diphosphate salt;2-(4-Imidazolyl)ethylamine diphosphate salt monohydrate;Histamine diphosphate salt monohydrat;Histamine bisphosphate monohydrate,2-(4-Imidazolyl)ethylamine diphosphate salt monohydrate, 2-(4-Imidazolyl)ethylamine diphosphate salt, Histamine diphosphate salt monohydrate;Histamine diphosphat;Histapon;HistaMine Diphosphate
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CAS No:
Description
Histamine diphosphate is a potent agonist of histamine receptors and vasodilator. It can activate nitric oxide synthetase.
White crystal
ChEBI: A phosphate salt that is the diphosphate salt of histamine.
Histamine bisphosphate monohydrate is an imidazole containing heterocyclic building block that can be employed in chemical synthesis. Its crystal structure belongs to the monoclinic space group,P21/cand shows O–H O and N–HO hydrogen bonds.
Histamine phosphate Basic Attributes
209.14
307.033
3744619
200-118-4
TSCA listed
DTXSID40218980
White
29332900
Characteristics
210
-0.31740
White Powder
128-132 °C
887.3ºC at 760 mmHg
490.4ºC
Soluble in water.
−20°C
-20°C
Safety Information
Ⅲ
3259
3
Xn
26-36-45-36/37/39-22
NI5425000
Xn
P261-P280-P305 + P351 + P338-P342 + P311
20/21/22-36/37/38-42/43-41-37/38-22
Histamine phosphate Use and Manufacturing
A potent histamine receptor agonist
Histamine diphosphate is a potent agonist of histamine receptors. It activates nitric oxide synthetase and is a potent vasodilator.
Computed Properties
Molecular Weight:209.14
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:209.05654287
Monoisotopic Mass:209.05654287
Topological Polar Surface Area:133
Heavy Atom Count:13
Complexity:115
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Stimulate the body to produce anti-histamine antibodies, thereby eliminating the pathogenic effects of endogenous histamine
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