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Glycerintrinitrat

Trinitroglycerin

HCID 4510
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Grundinformationen

CAS
55-63-0
Standard-SMILES
O=[N+]([O-])OCC(CO[N+](=O)[O-])O[N+](=O)[O-]
InChIKey
SNIOPGDIGTZGOP-UHFFFAOYSA-N
Summenformel
C3H5N3O9
Durchschnittliche Molmasse
227,085 g/mol
Monoisotopische Masse
227,00257874

Namen und Bezeichner

Bevorzugter Name
Trinitroglycerin
IUPAC
Propane-1,2,3-triyl trinitrate
Lokaler Name
Glycerintrinitrat
Englischer Name
Nitroglycerin
Summenformel
C3H5N3O9
Molmasse
227.09

Namen und Synonyme

Glyceryl trinitrateNITROGLYCERINENTGDiluted NitroglycerinTNGGTNNitrolingualNitroglicerinaSNGNitrol

Datenbank-Bezeichner

CAS
55-63-0
PubChem CID
4510
DTXSID
DTXSID1021407
ChEMBL
CHEMBL730
ChEBI
CHEBI:28787
UNII
G59M7S0WS3
EC Number
200-240-8
Nikkaji
J4.491A

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
2.8 °; · 2.8°; mp 13.5°
Siedepunkt
368.78 °C · 368.78°C (rough estimate)
Dichte
1515 · d1515 1.599; d44 1.6144; d415 1.6009; d425 1.5918
Brechungsindex
15 · nD15 1.474
Flammpunkt
12 °C · 12°C
storage temp.
-20 °C · -20°C
Löslichkeit
Miscible with acetone and with anhydrous ethanol
Aggregatzustand
solution
Wasserlöslichkeit
1.25 g/L · 1.25g/L(25 ºC)
Spezifische Wärmekapazität
1.03 J/ · Cp(gas): 1.03 J/(g·K), at 25℃
Henry's Law Constant
2.3 · 2.3×102 mol/(m3Pa) at 25℃, HSDB (2015)
Dielectric constant
19 · 19.0(20℃)
BCS Class
1 · 1
Major Application
pharmaceutical (small molecule)
InChI
1S/C3H5N3O9/c7-4(8)13-1-3(15-6(11)12)2-14-5(9)10/h3H,1-2H2
InChIKey
SNIOPGDIGTZGOP-UHFFFAOYSA-N
SMILES
O=[N+]([O-])OCC(CO[N+]([O-])=O)O[N+]([O-])=O
CAS Datenbank
55 · 55-63-0(CAS DataBase Reference)
NIST chemische Informationen
1 · 1,2,3-Propanetriol, trinitrate(55-63-0)
EPA chemische Informationen
Nitroglycerin (55-63-0)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

OEL
STEL: 0.1 mg/m3 [skin]
wgk
3
IDLA
75 mg/m3
tsca
TSCA listed
ridadr
UN 3064 3/PG II (NITROGLYCERIN, SOLUTION IN ALCOHOL with more than 1 % but not more than 5 % nitroglycerin)
hs_code
2920900002
risk_code
11-51/53-33-26/27/28-3-36-20/21/22-23/24/25
Toxizität
LD50 oral in rabbit: 1607mg/kg
hazard_code
E,T+,N,Xn,T
safety_code
7-16-61-45-36/37-35-33-26
hazard_class
1.1A
packing_group
I
Speicherklasse
3 - Flammable liquids
Giftige Stoffe Daten
55-63-0(Hazardous Substances Data)
Hazard Classifications
Acute Tox. 3 DermalAcute Tox. 4 OralFlam. Liq. 2

Chemie und Industrie

Anwendungen · 4 Einträge

Beschreibung3. S o n s t i g e s Nitrazingelb ist ein säureempfindlicher Farbstoff und wird in der analytischen Chemie als pH-Indikator im Bereich von pH 6,0 bis 7,0 eingesetzt.

BeschreibungNitroglycerin is an oily, poisonous, clear to pale yellow, explosive liquid.Nitroglycerin is made by nitrating glycerol. Early industrial processes used a batch process in which glycerol was added to a mixture with approximately equal volumes of nitric acid and sulfuric acid.The sulfuric acid serves to ionize the nitric acid and removes water formed in the nitration process.

HistoryIt was first prepared in 1846 by the Italian chemist Ascanio Sobrero (1812–1888), who nitrated glycerol using a mixture of nitric acid and sulfuric acid. Sobrero, who was injured in an explosion doing his research, realized the compound’s danger and abandoned work on nitroglycerin. Twenty years after Sobrero’s discovery, Alfred Nobel (1833–1896) developed its use commercially. Nobel mixed nitroglycerin with other substances, searching for a safe way to transport it and make it less sensitive to heat and pressure.nitroglycerin when it was first marketed,and Nobel continued to experiment with methods to make nitroglycerin safer.One of these was mixing nitroglycerin with materials to make a solid form of nitroglycerin. Nobel discovered that when nitroglycerin was mixed with a silica-based diatomaceous earth material called kieselguhr,a relatively stable product resulted.The mixture produced a paste that Nobel could pack into cardboard tubes;these could then be inserted into holes drilled into rock structures and detonated.In 1867,Nobel patented his mixture and called it dynamite,a name derived from the Greek word dunamis, meaning power.Nobel also perfected a blasting cap made from mercury fulminate (Hg(ONC)2) and potassium chlorate (KClO3) to detonate the nitroglycerin.

VerwendenNitroglycerin has medicinal use as a vasodilator. The main medical use of nitroglycerin is to treat angina pectoris. Nitroglycerin was first used to treat this condition in the late 19th century. It is prescribed today in various forms (tablet, ointment, patches, and injection) for patients who suffer from angina pectoris. Nitroglycerin is marketed under various trade names: Nitro-Dur, Nitrostat, Nitrospan, Nitro-Bid, and Tridil. When used in medications, the name glyceryl trinitrate is often used instead of nitroglycerin.

Vor- und nachgelagerte Produkte

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1
Reaktionsaufzeichnung erstellen
Reaktionsgleichung von HRID 1156505
HRID 1156505als Produktuspto-grants-1982_06

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Vorgelagerte Rohstoffe

SalpetersureSchwefelsureGlycerolEthanol

Nachgelagerte Produkte

1,2-DINITROGLYCERIN2-MONONITROGLYCERIN1,3-DINITROGLYCERIN

Ergänzende Hinweise

DefinitionChEBI: A nitroglycerol that is glycerol in which the hydrogen atoms of all three hydroxy groups are replaced by nitro groups. It acts as a prodrug, releasing nitric oxide to open blood vessels and so alleviate heart pain.