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N-Hydroxyurethane

N-Hydroxyurethane Suppliers list
Company Name: Capot Chemical Co.,Ltd.
Tel: 571-85586718 +8613336195806
Email: sales@capotchem.com
Products Intro: Product Name:N-Hydroxyurethane
CAS:589-41-3
Purity:97%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: CAS:589-41-3
Purity:0.99 Package:5G,10G,25G,50G,100G,250G,1KG
Company Name: Alfa Chemistry
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Products Intro: Product Name:N-Hydroxyurethane
CAS:589-41-3
Company Name: Aston Chemical
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Products Intro: Product Name:N-Hydroxyurethane
CAS:589-41-3
Company Name: Dayang Chem (Hangzhou) Co.,Ltd.
Tel: 571-88938639 +8617705817739
Email: info@dycnchem.com
Products Intro: Product Name:N-Hydroxyurethane
CAS:589-41-3
Purity:0.95&0.99 Package:0.1KG;1KG;1000KG Remarks:Hot selling
N-Hydroxyurethane Basic information
Product Name:N-Hydroxyurethane
Synonyms:n-hydroxyethylcarbamate;NSC-71045;NSC-83629;SQ 16819;N-HYDROXYURETHAN;N-HYDROXYURETHANE;N-HYDROXYURETHAN 94+%;Ethyl hydroxycarbamate 97%
CAS:589-41-3
MF:C3H7NO3
MW:105.09
EINECS:209-648-0
Product Categories:Amines;Mutagenesis Research Chemicals;Aliphatics;Hydroxylamines;Hydroxylamines (N-Substituted)
Mol File:589-41-3.mol
N-Hydroxyurethane Structure
N-Hydroxyurethane Chemical Properties
Boiling point 113-116 °C3 mm Hg(lit.)
density 1.3895 (rough estimate)
refractive index n20/D 1.445(lit.)
Fp >230 °F
storage temp. -20°C
solubility Diethyl Ether, Dimethyl Sulfoxide, Water
form Oil
pka9.30±0.23(Predicted)
color Yellow
BRN 1747529
CAS DataBase Reference589-41-3(CAS DataBase Reference)
NIST Chemistry ReferenceCarbamic acid, hydroxy-, ethyl ester(589-41-3)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
WGK Germany 2
RTECS FB1750000
HS Code 2928009090
ToxicityLD50 intraperitoneal in rat: 800mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
N-Hydroxyurethane Usage And Synthesis
Chemical PropertiesYellow Oil
UsesReactant 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
UsesHydroxyurethane is a metabolite of carcinogenic Urethane (U825300).
Biochem/physiol ActionsN-Hydroxyurethane causes the chromosomal fragmentation at millimolar concentrations and cell toxicity in cultured normal human leukocytes.
N-Hydroxyurethane Preparation Products And Raw materials
Tag:N-Hydroxyurethane(589-41-3) Related Product Information
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