ChemicalBook > CAS DataBase List > N-Hydroxyurethane

N-Hydroxyurethane

Product Name
N-Hydroxyurethane
CAS No.
589-41-3
Chemical Name
N-Hydroxyurethane
Synonyms
NHU;SQ 16819;NSC-71045;NSC-83629;85.0%(GC&HYDROXYURETHAN;Hydroxyurethane;N-HYDROXYURETHAN;N-HYDROXYURETHANE;N-Hydroxyurethane>
CBNumber
CB2725765
Molecular Formula
C3H7NO3
Formula Weight
105.09
MOL File
589-41-3.mol
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N-Hydroxyurethane Property

Boiling point:
113-116 °C3 mm Hg(lit.)
Density 
1.3895 (rough estimate)
refractive index 
n20/D 1.445(lit.)
Flash point:
>230 °F
storage temp. 
-20°C
solubility 
Diethyl Ether, Dimethyl Sulfoxide, Water
form 
Oil
pka
9.30±0.23(Predicted)
color 
Yellow
BRN 
1747529
CAS DataBase Reference
589-41-3(CAS DataBase Reference)
NIST Chemistry Reference
Carbamic acid, hydroxy-, ethyl ester(589-41-3)
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Safety

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
2
RTECS 
FB1750000
HS Code 
2928009090
Toxicity
LD50 intraperitoneal in rat: 800mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
119474
Product name
N-Hydroxyurethane
Packaging
5g
Price
$246
Updated
2023/06/20
Sigma-Aldrich
Product number
119474
Product name
N-Hydroxyurethane
Packaging
25g
Price
$531
Updated
2022/05/15
TCI Chemical
Product number
H0618
Product name
N-Hydroxyurethane
Purity
>85.0%(GC)(N)
Packaging
1g
Price
$31
Updated
2024/03/01
TCI Chemical
Product number
H0618
Product name
N-Hydroxyurethane
Purity
>85.0%(GC)(N)
Packaging
5g
Price
$109
Updated
2024/03/01
TRC
Product number
H991050
Product name
Hydroxyurethane
Packaging
25g
Price
$395
Updated
2021/12/16
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N-Hydroxyurethane Chemical Properties,Usage,Production

Chemical Properties

Yellow Oil

Uses

Hydroxyurethane is a metabolite of carcinogenic Urethane (U825300).

Uses

Reactant involved in:

  • Synthesis of molecules used for intermolecular Sharpless aminohydroxylation reactions
  • Intermolecular ortho-C-H amidation of anilides
  • Cinchona alkaloid-catalyzed asymmetric cycloaddition
  • Allylic arylation

Biochem/physiol Actions

N-Hydroxyurethane causes the chromosomal fragmentation at millimolar concentrations and cell toxicity in cultured normal human leukocytes.

N-Hydroxyurethane Preparation Products And Raw materials

Raw materials

Preparation Products

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N-Hydroxyurethane Suppliers

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589-41-3, N-HydroxyurethaneRelated Search:

Trinexapac-ethyl Urethane ETHYL ANTHRANILATE Benzocaine Triethyl orthoformate Ethyl acetate ISOXADIFEN-ETHYL Ethyl acrylate Ethyl formate Ethanol Ethyl cyanoacetate Ethylparaben Ethyl 4-(butylamino)benzoate Ethyl propiolate tert-Butyl (Mesitylsulfonyl)oxycarbaMate tert-Butyl N-hydroxycarbamate Ethyl chloroformate BENZYL N-HYDROXYCARBAMATE

  • ETHYL HYDROXYCARBAMATE
  • ETHYL N-HYDROXYCARBAMATE
  • HYDROXYCARBAMIC ACID ETHYL ESTER
  • Ethylester kyseliny N-hydroxykarbaminove
  • Ethyl Hydroxycarbamate Hydroxycarbamic Acid Ethyl Ester
  • <i>N</i>-Hydroxyurethane
  • ethylesterkyselinyn-hydroxykarbaminove
  • hydroxy-carbamicaciethylester
  • Hydroxyurethane
  • N-Carbethoxyhydroxylamine
  • NHU
  • N-Hydroxy ethyl carbamate
  • n-hydroxyethylcarbamate
  • NSC-71045
  • NSC-83629
  • SQ 16819
  • N-HYDROXYURETHAN
  • N-HYDROXYURETHANE
  • N-HYDROXYURETHAN 94+%
  • Ethyl hydroxycarbamate 97%
  • HYDROXYURETHAN
  • N-hydroxycarbamic acid ethyl ester
  • N-Hydroxycarbamic acid ethyl
  • N-Hydroxyurethane&gt
  • 85.0%(GC&amp
  • Carbamic acid, N-hydroxy-, ethyl ester
  • 589-41-3
  • HONHCOOCH2CH3
  • Hydroxylamines
  • Hydroxylamines (N-Substituted)
  • Organic Building Blocks
  • Nitrogen Compounds
  • Protected Amines
  • Building Blocks
  • Amines
  • Mutagenesis Research Chemicals
  • Aliphatics
  • Hydroxylamines
  • Hydroxylamines (N-Substituted)