structure of (Hydroxymethyl)urea

(Hydroxymethyl)urea

CAS No.: 1000-82-4
M. Wt: 90.08120
M. Fa: C2H6N2O2
InChI Key: VGGLHLAESQEWCR-UHFFFAOYSA-N

Names and Identifiers of (Hydroxymethyl)urea

CAS Number

1000-82-4

EC Number

213-674-8

IUPAC Name

hydroxymethylurea

InChI

InChI=1S/C2H6N2O2/c3-2(6)4-1-5/h5H,1H2,(H3,3,4,6)

InChIKey

VGGLHLAESQEWCR-UHFFFAOYSA-N

Canonical SMILES

C(NC(=O)N)O

UNII

15BY095DMS

Physical and chemical properties of (Hydroxymethyl)urea

Boiling Point

237.6ºC at 760 mmHg

Density

1.311 g/cm3

Exact Mass

90.04290

Flash Point

97.5ºC

Melting Point

111 °C

Molecular Formula

C2H6N2O2

Molecular Weight

90.08120

PSA

75.35000

Solubility

VERY SOL IN WATER; SOL IN METHANOL, ACETIC ACID; SOL IN HOT ALCOHOL; INSOL IN ETHER

Vapour Pressure

0.00326mmHg at 25°C

Safety Information of (Hydroxymethyl)urea

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of (Hydroxymethyl)urea

(Hydroxymethyl)urea finds diverse applications across various fields:

  • Polymer Chemistry: It serves as a modifier and plasticizer for urea-formaldehyde resins, enhancing the material properties of these polymers.
  • Cosmetics: Used in cosmetic formulations for its moisturizing properties.
  • Corrosion Inhibition: Effective as an inhibitor for steel corrosion in acidic environments, making it valuable in industrial applications.

Interaction Studies of (Hydroxymethyl)urea

Studies on the interaction of (hydroxymethyl)urea with other compounds reveal its potential as a corrosion inhibitor. For example, it has been shown to enhance the protective qualities of coatings applied to metals when exposed to corrosive environments like hydrochloric acid. Additionally, its interactions with biological molecules could lead to novel therapeutic applications.

Biological Activity of (Hydroxymethyl)urea

Research indicates that (hydroxymethyl)urea exhibits various biological activities. It has been shown to possess anti-corrosive properties, making it useful in protecting metals from acidic corrosion. Furthermore, studies suggest that derivatives of (hydroxymethyl)urea may have potential applications in pharmaceuticals due to their ability to interact with biological systems effectively.

Retrosynthesis analysis of (Hydroxymethyl)urea

  • Route#1

    Cas:13547-17-6
    Cas:1000-82-4
  • Route#2

    Cas:13547-17-6
    Cas:7732-18-5
    Cas:1000-82-4
  • Route#3

    Cas:140-95-4
    Cas:1000-82-4