File:Nitroglycerin.svg · Wikimedia Commons · See Wikimedia Commons
نیتروگلیسرین
Sign in to saveAlso known as glyceryl trinitrate, trinitroglycerin, nitroglycerine, trinitroglycerol, nitroglycerol, glycerol, nitric acid triester, 1,2,3-propanetrioltrinitrate, 1,2,3-propanetriyl nitrate
یک ترکیب شیمیایی
OverviewAI-generated
Nitroglycerin is a chemical compound with the formula C₃H₅N₃O₉. Its IUPAC name is 1,3-dinitrooxypropan-2-yl nitrate. The substance was discovered in 1847. It has a molecular mass of 227.003 and a density of 1.60.
Physical properties include a melting point of 56 and a decomposition point of 140. The vapor pressure is 0.0003, and solubility is 0.1. The compound has a charge of 0, with 9 hydrogen bond acceptors and 0 hydrogen bond donors. Its xlogp value is 1.6, and the topological polar surface area is 165.
Exposure limits are defined for safety, with a ceiling exposure limit of 2 and a short-term exposure limit of 0.1. The immediately dangerous to life or health level is 75. The defined daily dose is 5.
Synthesized by Vinony from 28 facts across 4 sources: Wikidata, PubChem, PubMed, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Chemical data
- Formula
- C3H5N3O9
- Molecular weight
- 227.09 g/mol
- IUPAC name
- 1,3-dinitrooxypropan-2-yl nitrate
- SMILES
- C(C(CO[N+](=O)[O-])O[N+](=O)[O-])O[N+](=O)[O-]
- InChIKey
- SNIOPGDIGTZGOP-UHFFFAOYSA-N
- XLogP
- 1.6
- Polar surface area
- 165 Ų
- H-bond donors
- 0
- H-bond acceptors
- 9
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 1981
- Admin. routes
- parenteral, topical
- Indications
- pain, stroke, osteoporosis, hypertension
via ChEMBL · EBI
Research
18,769 papers- Transdermal nitroglycerin (glyceryl trinitrate). A review of its pharmacology and therapeutic use.ReviewDrugs · 1990Todd PA, Goa KL, Langtry HDDOI: 10.2165/00003495-199040060-00009
- Intravenous glyceryl trinitrate (nitroglycerin). A review of its pharmacological properties and therapeutic efficacy.ReviewDrugs · 1984Sorkin EM, Brogden RN, Romankiewicz JADOI: 10.2165/00003495-198427010-00003
- Effect of Nitroglycerin on the Performance of MR Coronary Angiography.Journal of magnetic resonance imaging : JMRI · 2017Heer T, Reiter S, Trißler M et al.DOI: 10.1002/jmri.25483
- Fresh nitroglycerin (glyceryl trinitrate).American heart journal · 1966Burch GE, DePasquale NPDOI: 10.1016/0002-8703(66)90171-2
- CORONARY VASODILATORS.ReviewDiseases of the chest · 1963FISCH S, DEGRAFF ACDOI: 10.1378/chest.44.5.533
- ANGINA PECTORIS.ReviewBiochemical clinics · 1963CHEVALIER H, DE BUSTAMENTE JS
- Transdermal glyceryl trinitrate.Anaesthesia · 1986Charters PDOI: 10.1111/j.1365-2044.1986.tb13095.x
- CORONAROGRAPHY.Bibliotheca cardiologica · 1964PAULIN S
via PubMed
Wikidata facts
- Subclass of
- nitrate ester
- Has part
- nitrogen
- Mass
- 227.003
- Has use
- medication
Show 21 more facts
- Commons category
- Nitroglycerin
- chemical formula
- C₃H₅N₃O₉
- NIOSH Pocket Guide ID
- 0456
- density
- 1.60
- legal status (medicine)
- boxed warning
- immediately dangerous to life or health
- 75
- melting point
- 13
- decomposition point
- 122
- vapor pressure
- 0.0003
- solubility
- 0.1
- ceiling exposure limit
- 2
- short-term exposure limit
- 0.1
- active ingredient in
- pharmaceutical preparation of nitroglycerin
- World Health Organisation international non-proprietary name
- glyceryl trinitrate
- canonical SMILES
- C(C(CO[N+](=O)[O-])O[N+](=O)[O-])O[N+](=O)[O-]
- time of discovery or invention
- 1847-00-00
- subject has role
- medication
- discoverer or inventor
- Ascanio Sobrero
- defined daily dose
- 5
- has characteristic
- flammable liquid
- significant drug interaction
- avanafil
Sources (7)
via Wikidata · CC0
Gallery (18)
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