2-NITRO-1-PROPANOL
2-NITRO-1-PROPANOL Basic information
- Product Name:
- 2-NITRO-1-PROPANOL
- Synonyms:
-
- 1-Propanol, 2-nitro-
- 2-Nitropropanol
- Ba 51-084789
- 2-NITROPROPANOL-1
- 2-NITRO-1-PROPANOL
- 2-nitropropan-1-ol
- EINECS 220-797-0
- 2-Nitro-1-propanol >=97%
- CAS:
- 2902-96-7
- MF:
- C3H7NO3
- MW:
- 105.09
- EINECS:
- 220-797-0
- Product Categories:
-
- C2 to C6
- Alcohols
- Oxygen Compounds
- Building Blocks
- C2 to C6
- Chemical Synthesis
- Organic Building Blocks
- Oxygen Compounds
- Mol File:
- 2902-96-7.mol
2-NITRO-1-PROPANOL Chemical Properties
- Melting point:
- -20°C (estimate)
- Boiling point:
- 72-74 °C/1 mmHg (lit.)
- Density
- 1.185 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.439(lit.)
- Flash point:
- 212 °F
- storage temp.
- 2-8°C
- pka
- 7.36±0.13(Predicted)
- form
- liquid (clear)
- color
- clear green-yellow
- Water Solubility
- Slightly soluble in water.
- BRN
- 1748592
Safety Information
- Safety Statements
- 23-24/25
- WGK Germany
- 3
- HS Code
- 29055900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
2-NITRO-1-PROPANOL Usage And Synthesis
Uses
2-Nitro-1-propanol is used in improved synthesis of 2,2,2-trinitroethyl ethers, inhibits methane production during in vitro ruminal fermentation.
Uses
2-Nitro-1-propanol was used in improved synthesis of 2,2,2-trinitroethyl ethers.
Uses
2-Nitro-1-propanol is used in an improved synthesis of 2,2,2-trinitroethyl ethers.
Definition
ChEBI: 2-nitro-1-propanol is a C-nitro compound.
General Description
2-Nitro-1-propanol inhibits methane production during in vitro ruminal fermentation. It is a useful antimicrobial supplement which reduces carriage of certain food-borne pathogens in animals.
Synthesis
50-00-0
79-24-3
2902-96-7
77-49-6
To a three-necked round-bottomed flask equipped with a stirring magnet, condenser tube, nitrogen inlet and outlet, and constant-pressure dropping funnel, nitroethane (10 g, 0.13 mol) and triethylamine (0.3 g, 10 mol%) were added sequentially. The resulting light yellow solution was stirred for 10 min and then 37% aqueous formaldehyde solution (21.6 g, 0.27 mol) was added slowly and dropwise over a period of 1 hr. The reaction mixture was stirred continuously at room temperature for 24 h, during which the progress of the reaction was monitored periodically by gas chromatography (GC) to confirm complete conversion of the feedstock. The reaction was terminated after 24 hours and the volatile components were removed using a rotary evaporator. A yellow solution was obtained, which was analyzed by GC to confirm the presence of two target products (2-nitro-1-propanol and 2-nitro-2-methyl-1,3-propanediol). The mixture could be used directly in the subsequent reaction without further purification.
References
[1] Patent: EP2468713, 2012, A1. Location in patent: Page/Page column 3-4
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