Conditions | Yield |
---|---|
With potassium fluoride; nitrylfluoride In acetonitrile at -30 - -20℃; | 90% |
With sulfuric acid; nitric acid In dichloromethane; water at 5℃; Cooling with ice; | 90% |
With sulfuric acid; nitric acid In dichloromethane at 0 - 20℃; for 18h; | 75.9% |
Conditions | Yield |
---|---|
With chloroform; nitric acid at -10℃; |
propyl nitrate
Conditions | Yield |
---|---|
With nitrylfluoride In acetonitrile |
Conditions | Yield |
---|---|
With methyl nitrite; ultra-zero air; nitrogen(II) oxide at 25.9℃; for 0.333333h; Product distribution; Rate constant; Irradiation; other alkyl peroxy radical generator (Cl2); |
propane
A
i-propyl nitrite
B
n-propyl nitrite
C
isopropyl nitrate
D
propyl nitrate
E
2-nitropropane
F
1-Nitropropane
Conditions | Yield |
---|---|
With dihydrogen peroxide; Nitrogen dioxide at 24.9℃; under 300.02 Torr; Rate constant; Product distribution; Mechanism; boric-acid-coated surface; various pressure and carrier-gas composition; | A 12 % Chromat. B 7 % Chromat. C 16 % Chromat. D 5 % Chromat. E 46 % Chromat. F 14 % Chromat. |
propane
A
i-propyl nitrite
B
isopropyl nitrate
C
propyl nitrate
D
2-nitropropane
E
1-Nitropropane
F
acetone
Conditions | Yield |
---|---|
With dihydrogen peroxide; oxygen; Nitrogen dioxide at 24.9℃; under 300.02 Torr; Rate constant; Product distribution; Mechanism; boric-acid-coated surface; various O2 concn.; |
Conditions | Yield |
---|---|
With silver nitrate In acetonitrile at 20℃; for 24h; |
2-(2-methyl-5-(4-(methylsulfonyl)phenyl)-1-phenyl-1H-pyrrol-3-yl)ethyl-1H-imidazole-1-carboxylate
propyl nitrate
2-(2-methyl-5-(4-(methylsulfonyl)phenyl)-1-phenyl-1H-pyrrol-3-yl)ethyl-3-(nitrooxy)propyl carbonate
Conditions | Yield |
---|---|
With pyridine; 1,8-diazabicyclo[5.4.0]undec-7-ene at 20℃; for 3h; | 68% |
propyl nitrate
2,4-dibenzyloxybenzaldehyde
2,4-Dibenzyloxybenzonitrile
Conditions | Yield |
---|---|
In water; acetic acid | 40% |
Conditions | Yield |
---|---|
Mehrtaegiges Stehenlassen.; |
Conditions | Yield |
---|---|
With propan-1-ol; sodium n-propoxide at 110℃; im Rohr; |
Conditions | Yield |
---|---|
With ethanol; ammonia at 100℃; |
propyl nitrate
diisopropyl n-butylphosphonate
phosphoric acid diisopropyl ester propyl ester
Conditions | Yield |
---|---|
(i) nBuLi, iPr2NH, THF, hexane, (ii) /BRN= 1701406/; Multistep reaction; |
propyl nitrate
dibutyl butylphosphonate
phosphoric acid dibutyl ester propyl ester
Conditions | Yield |
---|---|
(i) nBuLi, iPr2NH, THF, hexane, (ii) /BRN= 1701406/; Multistep reaction; |
1,2-dimethyl-1H-benzimidazole
propyl nitrate
1-methyl-2-nitromethylbenzimidazole
Conditions | Yield |
---|---|
With ammonia; sodium 1.30min 2. 30min, ether; Yield given. Multistep reaction; |
2'-hydroxy-3',4'-dimethoxyacetophenone
propyl nitrate
1-(2-Hydroxy-3,4-dimethoxy-phenyl)-2-nitro-ethanone
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
propyl nitrate
1-(2-Hydroxy-phenyl)-propan-1-on
A
propyl salicylate
B
2-((Z)-1-Hydroxy-2-nitro-propenyl)-phenol
C
salicylic acid
Conditions | Yield |
---|---|
Yield given. Multistep reaction. Yields of byproduct given; |
propyl nitrate
3-Hydroxyacetophenone
A
Propyl 3-hydroxybenzoate
B
1-(3-Hydroxy-phenyl)-2-nitro-ethanone
Conditions | Yield |
---|---|
Yield given. Multistep reaction. Yields of byproduct given; |
propyl nitrate
1-(2-hydroxyphenyl)-2-methylpropan-1-one
A
propyl salicylate
B
1-(2-Hydroxy-phenyl)-2-methyl-2-nitro-propan-1-one
C
salicylic acid
Conditions | Yield |
---|---|
Yield given. Multistep reaction. Yields of byproduct given; |
propyl nitrate
o-hydroxyacetophenone
A
2'-Hydroxy-ω-nitroacetophenone
B
propyl salicylate
Conditions | Yield |
---|---|
Yield given. Multistep reaction. Yields of byproduct given; |
propyl nitrate
2-methyl-1-phenyl-1H-benzimidazole
1-phenyl-2-nitromethylbenzimidazole
Conditions | Yield |
---|---|
With ammonia; sodium 1. 30min 2. 30min, ether; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
at 181℃; Rate constant; Pyrolysis; |
Conditions | Yield |
---|---|
Zersetzt beim Erhitzen an der Luft explosionsartig; |
propyl nitrate
Conditions | Yield |
---|---|
With hydrogenchloride; n-butyllithium; sodium bicarbonate In tetrahydrofuran; hexane; water |
propyl nitrate
3,4-dibromoacetanilide
acetic acid-(4,5-dibromo-2-nitro-anilide)
Conditions | Yield |
---|---|
With sulfuric acid In ice-water | |
With sulfuric acid In ice-water | |
With sulfuric acid |
propyl nitrate
Nitrogen dioxide
Conditions | Yield |
---|---|
In gaseous matrix Irradiation (UV/VIS); photolysis of alkyl nitrate (pressure 1-10 Torr) at 278-293 K; N2 buffergas; |
Conditions | Yield |
---|---|
-70°C; |
Empirical Formula: C3H7NO3
Molecular Weight: 105.09 g/mol
EINECS: 210-985-0
Index of Refraction: 1.402
Density: 1.081 g/cm3
Flash Point: 42.2 °C
Enthalpy of Vaporization: 33.57 kJ/mol
Boiling Point: 111.6 °C at 760 mmHg
Vapour Pressure: 26.6 mmHg at 25 °C
Solubility: Insoluble in water
Appearance: A white to straw-colored liquid with an ether-like odor
Structure of n-Propyl nitrate (CAS NO.627-13-4):
IUPAC Name of n-Propyl nitrate (CAS NO.627-13-4): Propyl nitrate
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
cat | LDLo | intravenous | 100mg/kg (100mg/kg) | Journal of Pharmacology and Experimental Therapeutics. Vol. 118, Pg. 77, 1956. | |
dog | LDLo | intravenous | 200mg/kg (200mg/kg) | Journal of Pharmacology and Experimental Therapeutics. Vol. 118, Pg. 77, 1956. | |
mouse | LCLo | inhalation | 5816ppm/4H (5816ppm) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD LUNGS, THORAX, OR RESPIRATION: CYANOSIS | American Industrial Hygiene Association Journal. Vol. 19, Pg. 80, 1958. |
rabbit | LD50 | intravenous | 200mg/kg (200mg/kg) | Journal of Pharmacology and Experimental Therapeutics. Vol. 118, Pg. 77, 1956. | |
rat | LCLo | inhalation | 5816ppm/4H (5816ppm) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: CYANOSIS | American Industrial Hygiene Association Journal. Vol. 19, Pg. 80, 1958. |
Reported in EPA TSCA Inventory.
Poison by intravenous route. Inhalation can cause hypotension and methemoglobinemia. Dangerous fire hazard when exposed to heat, flame, or oxidizers. Explosive in the form of vapor when exposed to heat or flame. A shock-sensitive explosive. It can be desensitized by the addition of 1–2% propane, butane, chloroform, dimethyl ether, or diethyl ether. When heated to decomposition it emits toxic fumes of NOx. Used as a fuel ignition promoter, chemical intermediate, and in the manufacture of rocket fuels. See also NITRATES and ESTERS.
OSHA PEL: TWA 25 ppm; STEL 40 ppm
ACGIH TLV: TWA 25 ppm; STEL 40 ppm
DFG MAK: 25 ppm (110 mg/m3)
DOT Classification: 3; Label: Flammable Liquid
n-Propyl nitrate ,its cas register number is 627-13-4. It also can be called Nitrate de propyle normal ; Nitric acid, propyl ester ;and Propyl nitrate . n-Propyl nitrate (CAS NO.627-13-4), range from slight to strong oxidizing agents and if mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation.
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