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| | 2,4-Dinitrophenol Basic information |
| | 2,4-Dinitrophenol Chemical Properties |
| Melting point | 108-112 °C (lit.) | | Boiling point | 318.03°C (rough estimate) | | density | 1,683 g/cm3 | | vapor density | 6.35 (vs air) | | vapor pressure | 39(x 10-5 mmHg) at 20 °C (Schwarzenbach et al., 1988) | | refractive index | 1.4738 (estimate) | | Fp | 11 °C | | storage temp. | 2-8°C | | solubility | Solubility Sparingly soluble in water; soluble in ethanol, benzene | | form | crystals | | pka | 3.96(at 15℃) | | color | Light yellow | | PH Range | 2.8(colourless)-4.7(yellow) | | Odor | Sweet, musty | | Water Solubility | 0.6 g/100 mL (18 ºC) | | Sensitive | Light Sensitive | | Merck | 14,3280 | | BRN | 1246142 | | Henry's Law Constant | 5.70 x 10-8(atm?m3/mol) at 5 °C (average derived from six field experiments, Lüttke and Levsen, 1997) | | Stability: | Stable. Combustible. | | Major Application | Display device, recording materials, inks, paints, method for preserving food, method for gene expression profiling, treatment of parasitic diseases, neurological diseases, epilepsy, cancer, keratin materials, neoplasms, infectious diseases, neutropenia, detecting chromosome aberrations, bacteria in gastrointestinal track | | CAS DataBase Reference | 51-28-5(CAS DataBase Reference) | | NIST Chemistry Reference | Phenol, 2,4-dinitro-(51-28-5) | | EPA Substance Registry System | 2,4-Dinitrophenol (51-28-5) |
| | 2,4-Dinitrophenol Usage And Synthesis |
| Chemical Properties | light yellow crystal powder | | Uses | Dinitrophenol is used in the manufacture of dyes, as a wood preservative, and as an indicator and analytical reagent. | | Uses | In manufacture of dyes, other organic
chemicals, wood preservatives, photographic
developer, and explosives | | Uses | 2,4-Dinitrophenol (DNP) can be used:
- As a reactant for catalytic reduction reactions.
- To activate carboxylic acids by converting them into dinitrophenyl (DNP) esters.
- To prepare the corresponding ester via acylation reaction using isobutyric anhydride catalyzed by hafnium triflate.
- As an effective cocatalyst to accelerate the activity and enantioselectivity of primary amine organocatalyst derived from natural primary amino acids for direct asymmetric aldol reaction.
- As an alternative activator to tetrazoles in the reaction of phosphoroamidites with nucleosides.
| | Definition | ChEBI: 2,4-dinitrophenol is a dinitrophenol having the nitro groups at the 2- and 4-positions. It has a role as an oxidative phosphorylation inhibitor, a bacterial xenobiotic metabolite, an antiseptic drug, an allergen and a geroprotector. It is a conjugate acid of a 2,4-dinitrophenol(1-). | | Synthesis Reference(s) | The Journal of Organic Chemistry, 60, p. 3445, 1995 DOI: 10.1021/jo00116a034 | | General Description | Solid yellow crystals. Explosive when dry or with less than 15% water. The primary hazard is from blast of an instantaneous explosion and not flying projectiles and fragments. slightly soluble in water and soluble in ether and solutions of sodium or potassium hydroxide. | | Air & Water Reactions | Highly flammable. Slightly soluble in water. | | Reactivity Profile | 2,4-Dinitrophenol may explode if subjected to heat or flame. may explode if allowed to dry out. Forms explosive salts with alkalis and ammonia. Incompatible with heavy metals and their compounds. Also incompatible with strong oxidizing agents, strong bases and reducing agents. Reacts with combustibles. | | Health Hazard | DUST: POISONOUS IF INHALED OR IF SKIN IS EXPOSED. SOLID: POISONOUS IF SWALLOWED. | | Health Hazard | 2,4-Dinitrophenol is a severely acute toxicant, exhibiting high toxicity in animals by all routes of administration. It can be absorbed through the intact skin. The toxic effects are heavy sweating, nausea, vomiting, collapse, and death. Ingestion of 1 g of solid can be fatal to humans. A 30-minute exposure to its vapors at a concentration of 300 mg/m3 was lethal to dogs (NIOSH 1986). Chronic effects include polyneuropathy, weight loss, cataracts, and dermatitis.
LD50 value, oral (rats): 30 mg/kg. | | Fire Hazard | Combustible. May explode if subjected to heat or flame. POISONOUS GAS IS PRODUCED WHEN HEATED. Vapors are toxic. Can detonate or explode when heated under confinement. | | Safety Profile | A deadly human poison
by ingestion. An experimental poison by
ingestion, inhalation, intravenous,
intraperitoneal, subcutaneous, and
intramuscular routes. Moderately toxic by
skin contact. Experimental teratogenic and
reproductive effects. Human systemic
effects: body temperature increase, change
in heart rate, coma. A skin irritant. Mutation
data reported. Phytotoxic. A pesticide. An
explosive. Forms explosive salts with alkalies
and ammonia. When heated to
decomposition it emits toxic fumes of NOx.
See also NITRO COMPOUNDS of
AROMATIC HYDROCARBONS. | | Carcinogenicity | No teratogenic effects have been reported
in limited developmental toxicity studies in
rodents. Decreased fetal body weight and
crown-rump length were noted in rats and
mice after parenteral administration.
2,4-DNP was not genotoxic in most in
vivo and in vitro studies.
An ACGIH threshold limit value (TLV)
has not been established for 2,4-DNP. | | Metabolic pathway | The bacterial strain RB1, which is isolated by
enrichment cultivation with 2,4-dinitrophenol, degrades
this phenol into two aliphatic acids. One metabolite
results from the release of the 2-nitro group as nitrile,
with the production of aliphatic nitro compound,
3-nitroadipate. Then, the 3-nitro group is released
from this metabolite as nitrile. The other metabolite is
4,6-dinitrohexanoic acid possessing two nitro groups
from 2,4-dinitrophenol. | | Purification Methods | Crystallise it from *benzene, EtOH, EtOH/H2O or H2O acidified with dilute HCl, dry it, then recrystallise it from CCl4. Dry it in an oven and store it in a vacuum desiccator over CaSO4. The benzoate has m 132o (from EtOH). [Beilstein 6 IV 1369.] |
| | 2,4-Dinitrophenol Preparation Products And Raw materials |
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