Diurea
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Diurea
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CAS No:
110-21-4
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Formula:
C2H6N4O2
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Chemical Name:
Diurea
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Synonyms:
1,2-Hydrazinedicarboxamide;Biurea;1,1′-Hydrazobis(formamide);Bicarbamamide;Hydrazodicarboxamide;Hydrazodicarbonamide;Hydrazine,1,2-bis(aminocarbonyl)-;Bicarbamimidic acid;Ureidourea;Hydrazocarbonamide;Hydrazinedicarboxylic acid diamide;Hydrazine-N,N′-bis(carboxamide);Hydradicarbonamide;N,N′-Biscarbamoylhydrazine;Hydrazodicarbamide;Cellmic 142;HDCA;S 3176;KBH 30;LDA;LDA (fire retardant);NSC 1897;Diurea;FE 823;(Carbamoylamino)urea;77107-48-3
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CAS No:
Description
WHITE POWDERWhite powder.
Biurea is a white powder. (NTP, 1992)
Biurea is a white powder. (NTP, 1992)
Diurea Basic Attributes
118.09
118.09
203-747-2
POJ4UOY01H
1897
DTXSID6024628
Plates from water
29280000
Characteristics
110
-2.1
Biurea is a white powder. (NTP, 1992)
1.604 g/cm3 @ Temp: -5 °C
258 °C
220.6°C (rough estimate)
153.7ºC
1.4462 (estimate)
In water, 238 mg/L at 16 deg C
5.9X10-5 mm Hg at 25 deg C /Estimated/
LD50 oral in rat: > 2gm/kg
Henry's Law constant = 1X10-19 atm-cu m/mol at 25 °C /Estimated/
Hydroxyl radical reaction rate constant = 4.0X10-12 cu cm/molec-sec at 25 °C /Estimated/
Insoluble in water.
Amides and Imides
BIUREA is chemically classified as an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Safety Information
IRRITANT
36/37/38
24/25
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
H315
SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.
The flash point of this compound is not available, however it is probably non-flammable. (NTP, 1992)
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Fires associated with this compound should be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
SMALL SPILLS AND LEAKAGE: If you spill this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then dampen the solid spill material with toluene, then transfer the dampened material to a suitable container. Use absorbent paper dampened with toluene to pick up any remaining material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent-wash all contaminated surfaces with toluene followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. STORAGE PRECAUTIONS: You should store this material in a refrigerator. (NTP, 1992)
RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)|... Vinyl coated hand protection, natural or reclaimed rubber protection, rubber aprons, and plastic eye and face protection ... used when working with small quantities. Where possibility of gross splashing exists, full protective clothing made of rubber, neoprene or vinyl-coated materials should be worn. For respiratory protection in situations where recommended tolerance limits are ... exceeded, respiratory protective equipment ... must be used. /Hydrazine and derivatives/
Inhalation of salt dusts should be avoided. /Hydrazine & derivatives/|Engineering controls, such as process enclosure or local exhaust ventilation, shall be used when needed to keep concentrations of airborne hydrazines within acceptable levels. Ventilation systems shall be designed to prevent accumulation or recirculation of airborne hydrazines in the workplace environment and to remove hydrazines from the breathing zone of workers. /Hydrazines/
Toxicity
LD50 Rat oral >2000 mg/kg
Biological half-lives were significantly different among the three acetylation phenotypes (analysis of variance, P < 0.05): 3.94+/-1.70 hours for slow acetylators, 2.25+/-0.37 hours for intermediate acetylators, and 1.86+/-0.67 hours for rapid acetylators. /Hydrazine/
Drug Information
/In animals/ the compound is mainly excreted in the feces and to a smaller part in the urine after oral dosing.|Two-week repeated and 13-week subchronic inhalation exposures of F344/N rats and B6C3F1 mice to /azodicarbonamide/ (ADA) were conducted ... . The mean air concentrations of ADA in the 2-week studies were 207, 102, 52, 9.4, or 2.0 mg/cu m. ... In the 13-week subchronic study, the mean air concentrations of ADA were 204, 100, or 50 mg/cu m. ... Lung tissue from male rats was analyzed for ADA and biurea, the major metabolite of ADA. No ADA was detected. The amount of biurea in the lungs increased nonlinearly with increasing exposure concentration, suggesting that clearance was somewhat impaired with repeated exposures. However, even at the highest exposure concentration, this amount of biurea was less than 1% of the estimated total ADA deposited over the exposure period. /Azodicarbonamide/
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)
Diurea Use and Manufacturing
The unsubstituted parent semicarbazide is best made from urea and hydrazine; using excess urea, hydrazodicarbonamide is formed.|/Hydrazodicarboxamide/ is made by refluxing an aqueous solution of urea and hydrazine.
Used in the production of ADC foaming agent
1,2-Hydrazinedicarboxamide: ACTIVE
Computed Properties
Molecular Weight:118.10
XLogP3:-2.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:2
Exact Mass:118.04907545
Monoisotopic Mass:118.04907545
Topological Polar Surface Area:110
Heavy Atom Count:8
Complexity:96.6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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