64-10-8

64-10-8
64-10-8
64-10-8

64-10-8

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100 Kilogram

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  • Min.Order :100 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

64-10-8 64-10-8 C7H8N2O

Quick Details

  • Appearance:powder
  • Application:64-10-8
  • PackAge:Depended
  • ProductionCapacity:300|Kilogram|Month
  • Storage:Refrigerator
  • Transportation:by air or by sea

Superiority:

PHENYLUREA Basic information
Product Name: PHENYLUREA
Synonyms: N-PHENYLUREA;PHENYLCARBAMIDE;PHENYLUREA;1-Phenylurea;Monophenylurea;phenyl-ure;phenylureapesticide,liquid,flammable,poisonous;phenylureapesticide,liquid,poisonous
CAS: 64-10-8
MF: C7H8N2O
MW: 136.15
EINECS: 200-576-5
Product Categories: Bioactive Small Molecules;Building Blocks;Carbonyl Compounds;Cell Biology;Chemical Synthesis;Organic Building Blocks;P;Ureas
Mol File: 64-10-8.mol
PHENYLUREA Structure
 
PHENYLUREA Chemical Properties
mp  145-147 °C(lit.)
bp  238 °C
density  1,302 g/cm3
vapor density  >1 (vs air)
Fp  238°C
solubility  H2O: 10 mg/mL, clear
Merck  14,7319
BRN  1934615
Stability: Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 64-10-8(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn
Risk Statements  22
Safety Statements  22-36/37
WGK Germany  3
RTECS  YU0650000
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
 
PHENYLUREA Usage And Synthesis
Chemical Properties off-white powder
General Description A solid or liquid absorbed on a dry carrier. A wettable powder. Contains any of several related products (Diuron, Fenuron, Linuron, Monuron, Neburon, Siduron) formally derived from urea. Toxic by inhalation, skin absorption, or ingestion. Obtain the technical name of the specific pesticide from the shipping papers and contact CHEMTREC, 800-424-9300 for response information.
Reactivity Profile Organic 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). Contains any of several related compounds (Diuron, Fenuron, Linuron, Neburon, Siduron, Monuron) formally derived from urea.
Health Hazard Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
Fire Hazard Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.
 
PHENYLUREA Preparation Products And Raw materials
Preparation Products 4-UREIDO-BENZENESULFONYL CHLORIDE-->4-PHENYLSEMICARBAZIDE-->1,4-DIPHENYLSEMICARBAZIDE
 
 
 

 

 

 

 

 

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