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Phenylurea

CAS No.
64-10-8
Chemical Name:
Phenylurea
Synonyms
1-Phenylurea;VH;N-PHENYLUREA;Urea, N-phenyl-;phenyl-ure;PHENYLUREA;stabilizervh;Urea,phenyl-;AKOS B029810;Stabilizer VH
CBNumber:
CB2252571
Molecular Formula:
C7H8N2O
Molecular Weight:
136.15
MDL Number:
MFCD00007944
MOL File:
64-10-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-18 09:57:46
Product description Number Pack Size Price
N-Phenylurea 97% P36959 100g $28.6
N-Phenylurea 97% P36959 500g $97
Phenylurea >98.0%(HPLC)(N) P0247 25g $30
Phenylurea >98.0%(HPLC)(N) P0247 100g $92
1-Phenylurea ≥98% CS-W017760 100g $12
More product size

Phenylurea Properties

Melting point 145-147 °C(lit.)
Boiling point 238 °C
Density 1,302 g/cm3
vapor density >1 (vs air)
refractive index 1.5769 (estimate)
Flash point 238°C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility H2O: 10 mg/mL, clear
pka 13.37±0.50(Predicted)
form Powder, Crystals and/or Chunks
color White to light yellow
Water Solubility Soluble in water.
Merck 14,7319
BRN 1934615
Stability Stable. Incompatible with strong oxidizing agents.
InChI 1S/C7H8N2O/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)
InChIKey LUBJCRLGQSPQNN-UHFFFAOYSA-N
SMILES NC(=O)Nc1ccccc1
CAS DataBase Reference 64-10-8(CAS DataBase Reference)
FDA UNII 862I85399W
EPA Substance Registry System Urea, phenyl- (64-10-8)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319
Precautionary statements  P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P501-P301+P312a-P330-P501a
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn
Risk Statements  22
Safety Statements  22-36/37-24/25
WGK Germany  3
RTECS  YU0650000
TSCA  TSCA listed
HS Code  29242100
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Toxicity LD50 oral in rat: 2gm/kg
NFPA 704
1
2 0

Phenylurea price More Price(40)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P36959 N-Phenylurea 97% 64-10-8 100g $28.6 2026-04-30 Buy
Sigma-Aldrich P36959 N-Phenylurea 97% 64-10-8 500g $97 2026-04-30 Buy
TCI Chemical P0247 Phenylurea >98.0%(HPLC)(N) 64-10-8 25g $30 2026-04-30 Buy
TCI Chemical P0247 Phenylurea >98.0%(HPLC)(N) 64-10-8 100g $92 2026-04-30 Buy
ChemScene CS-W017760 1-Phenylurea ≥98% 64-10-8 100g $12 2026-06-04 Buy
Product number Packaging Price Buy
P36959 100g $28.6 Buy
P36959 500g $97 Buy
P0247 25g $30 Buy
P0247 100g $92 Buy
CS-W017760 100g $12 Buy

Phenylurea Chemical Properties,Uses,Production

Herbicide residues

According to European Union regulations, the maximum residue level (MRL) for a single phenylurea herbicide is 0.1 μg/L in drinking water and 0.01–0.05 mg/kg in food (Commission Directive 2019/1792/EC)[1].

Chemical Properties

Colorless needle-like crystals or off-white powder. Melting point 147°C(decomposition), soluble in hot water, hot alcohol, ether, ethyl acetate and acetic acid.

Uses

Phenylureas are commonly used soil-applied herbicides for control of grass and small-seeded broadleaf weeds.

Uses

Phenyl urea is used in organic synthesis. It acts as an efficient ligand for palladium-catalyzed Heck and Suzuki reactions of aryl bromides and iodides.

Preparation

Phenylurea is synthesized by the reaction of aniline and urea. Put urea, hydrochloric acid and aniline into the reaction pot, heat and stir, reflux at 100-104°C for 1 hour, add water and stir, cool, filter, wash the filter cake with water, and dry to obtain the finished product of phenylurea.

Application

Phenyl urea pesticide, liquid, poisonous appears as a liquid dissolved or suspended in a liquid carrier. Contains any of several related compounds (Diuron, Fenuron, Linuron, Neburon, Siduron, Monuron) formally derived from urea. Carrier is water emulsifiable. Toxic by inhalation, skin absorption, or ingestion.

Definition

ChEBI: 1-Phenylurea is a member of ureas.

General Description

Phenylurea is the core structural unit of phenylurea herbicides (PUHs), such as diuron, fenuron, linuron, monuron, isoproturon, monolinuron and chlortoluron. As photosynthesis inhibitors, phenylurea herbicides are widely used in various crops for the pre-emergence and post-emergence control of broadleaf and annual weeds. These herbicides are used on major food crops, including maize (Zea mays) and tomato (Solanum lycopersicum), to control weeds such as lamb’s quarters (Chenopodium album), amaranth (Amaranthus spp.) and barnyard grass (Echinochloa crus-galli)[1].

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.

Purification Methods

Crystallise the urea from boiling water (10mL/g) or amyl alcohol (m 149o). Dry it in a steam oven at 100o. The 1:1 resorcinol complex has m 115o (from EtOAc/*C6H6). [Beilstein 12 H 346, 12 II 204, 12 III 760, 12 IV 734.]

References

[1] Xue-Ying Rui . (2025). Construction of covalent organic framework electrospun composite nanofiber membranes for the efficient extraction and detection of phenylurea herbicides. Food Chemistry, 496, Article 146787. https://doi.org/10.1016/j.foodchem.2025.146787

55-21-0
64-10-8
Synthesis of Phenylurea from Benzamide
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Q:What are the common phenylurea herbicides?STAR - Jun 15,2026
A:Phenylurea herbicides are an important class of pesticides widely used worldwide for weed control in cotton, fruit trees and cereal crops, both before and after emergence. Common phenylurea herbicides include: Diuron, Monuron, Linuron, Fenuron, Isoproturon, Metobromuron, Buturon, Neburon, Monolinuron, Chlorotoluron, Fluometuron, Methabenzthiazuron, etc.

View Lastest Price from Phenylurea manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Phenylurea pictures 2026-07-27 Phenylurea
64-10-8
$15.00 1KG 99% 200 tons/ year Speranza Chemical Co., Ltd.
N-Phenylurea pictures 2026-07-13 N-Phenylurea
64-10-8
1KG 99%Min 3000 tons Xi’an Goldenfeather & One Technology Co., Ltd.
Phenylurea pictures 2026-03-20 Phenylurea
64-10-8
$10.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
  • Phenylurea pictures
  • Phenylurea
    64-10-8
  • $15.00
  • 99%
  • Speranza Chemical Co., Ltd.
  • N-Phenylurea pictures
  • N-Phenylurea
    64-10-8
  • 99%Min
  • Xi’an Goldenfeather & One Technology Co., Ltd.
  • Phenylurea pictures
  • Phenylurea
    64-10-8
  • $10.00
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd
Monophenylurea PHENYLCARBAMIDE PHENYLUREA phenyl-ure phenylureapesticide,liquid,flammable,poisonous phenylureapesticide,liquid,poisonous phenylureapesticide,solid,poisonous Stabilisator VH N-Phenylurea,Phenylcarbamide N-PHENYLUREA FOR SYNTHESIS 250 G N-PHENYLUREA FOR SYNTHESIS 5 G N-Phenylurea 97% N-Phenylurea Vetec(TM) reagent grade, 97% stabilisatorvh Stabilizer VH stabilizervh Urea,phenyl- Phenylcarbamidel AKOS B029810 CHEMPACIFIC 39929 Phenylurea,97% Phenylurea, mono- N-Phenylurea,Phenylcarbamidel PHENY CARBAMIDE (Phenylamino)formamide Phenylurea> Phenylurea, 98%, for synthesis Urea, N-phenyl- Althiazide Impurity 2(Althiazide EP Impurity B) N'-phenyl Urea N-Phenylurea 1-Phenylurea N-PHENYLUREA VH 64-10-8 1964-10-8 1964-10-08 C7H8N2O1 C7H8N20 C6H5NHCONH2 Building Blocks Carbonyl Compounds Organic Building Blocks Ureas Bioactive Small Molecules Building Blocks Carbonyl Compounds Cell Biology Chemical Synthesis Organic Building Blocks P Ureas