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.

P501Dispose of contents/container to..…

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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

Americas 1 Belgium 1 Canada 3 China 57 Europe 2 France 2 Germany 4 India 3 Japan 1 Switzerland 1 The Netherlands 1 United Kingdom 10 United States 29 Global 115

J & K SCIENTIFIC LTD.

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TCI (Shanghai) Development Co., Ltd.

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Energy Chemical

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Shanghai Hanhong Scientific Co.,Ltd.

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Chemsky（shanghai）International Co.,Ltd.

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Thermo Fisher Scientific

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Nanjing Norris-Pharm Technology Co., Ltd

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Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.

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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)