Basic information Safety Supplier Related

2-NITRO-1-PROPANOL

Basic information Safety Supplier Related

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
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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
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Safety Information

Safety Statements 
23-24/25
WGK Germany 
3
HS Code 
29055900

MSDS

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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

2-NITRO-1-PROPANOLSupplier

Alfa Aesar
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