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N-Hydroxyurethane

N-Hydroxyurethane structure

CAS No.: 589-41-3

Chemical Name:: N-Hydroxyurethane

Synonyms: NHU;SQ 16819;NSC-83629;NSC-71045;85.0%(GC&HYDROXYURETHAN;Hydroxyurethane;N-HYDROXYURETHAN;N-HYDROXYURETHANE;N-Hydroxyurethane>

CBNumber:: CB2725765

Molecular Formula:: C3H7NO3

Molecular Weight:: 105.09

MDL Number:: MFCD00002108

MOL File:: 589-41-3.mol

Last updated:2023-06-08 17:06:36

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N-Hydroxyurethane Properties

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)
FDA UNII	QWI3C4ASI7
NIST Chemistry Reference	Carbamic acid, hydroxy-, ethyl ester(589-41-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)

GHS07

Signal word

Warning

Hazard statements

H302+H312+H332

Precautionary statements

P501-P261-P270-P271-P264-P280-P362+P364-P301+P312+P330-P302+P352+P312-P304+P340+P312

Risk Statements

36/37/38

Safety Statements

26-36/37/39

WGK Germany

RTECS

FB1750000

HS Code

2928009090

Toxicity

LD50 intraperitoneal in rat: 800mg/kg

NFPA 704

	1
0		1

N-Hydroxyurethane price More Price(12)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich	119474	N-Hydroxyurethane	589-41-3	5g	$246	2023-06-20	Buy
Sigma-Aldrich	119474	N-Hydroxyurethane	589-41-3	25g	$531	2022-05-15	Buy
TCI Chemical	H0618	N-Hydroxyurethane >85.0%(GC)(N)	589-41-3	1g	$31	2024-03-01	Buy
TCI Chemical	H0618	N-Hydroxyurethane >85.0%(GC)(N)	589-41-3	5g	$109	2024-03-01	Buy
TRC	H991050	Hydroxyurethane	589-41-3	25g	$395	2021-12-16	Buy

Product number	Packaging	Price	Buy
119474	5g	$246	Buy
119474	25g	$531	Buy
H0618	1g	$31	Buy
H0618	5g	$109	Buy
H991050	25g	$395	Buy

N-Hydroxyurethane Chemical Properties,Uses,Production

Chemical Properties

Yellow Oil

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

Uses

Hydroxyurethane is a metabolite of carcinogenic Urethane (U825300).

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

N-Hydroxyurethane Suppliers

Global( 109)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
Capot Chemical Co.,Ltd.	571-85586718 +8613336195806	sales@capotchem.com	China	29797	60
ATK CHEMICAL COMPANY LIMITED	+undefined-21-51877795	ivan@atkchemical.com	China	32480	60
Alfa Chemistry		info@alfa-chemistry.com	United States	2344	58
Aston Chemical	13000000000	sales@astonchem.com	United States	1634	58
Dayang Chem (Hangzhou) Co.,Ltd.	571-88938639 +8617705817739	info@dycnchem.com	CHINA	52867	58
LEAP CHEM CO., LTD.	+86-852-30606658	market18@leapchem.com	China	24738	58
Hebei Guanlang Biotechnology Co., Ltd.	+86-19930503259 +86-19930503259	cherry@crovellbio.com	China	18458	58
GIHI CHEMICALS CO.,LIMITED	+8618058761490	info@gihichemicals.com	China	49999	58
Shanghai Acmec Biochemical Technology Co., Ltd.	+undefined18621343501	product@acmec-e.com	China	33349	58
Nanjing Bicbiotechnology Co., Ltd	+86-2552131256 +86-18251840740	sales@bicbiotech.com	China	6000	58

Supplier	Advantage
Capot Chemical Co.,Ltd.	60
ATK CHEMICAL COMPANY LIMITED	60
Alfa Chemistry	58
Aston Chemical	58
Dayang Chem (Hangzhou) Co.,Ltd.	58
LEAP CHEM CO., LTD.	58
Hebei Guanlang Biotechnology Co., Ltd.	58
GIHI CHEMICALS CO.,LIMITED	58
Shanghai Acmec Biochemical Technology Co., Ltd.	58
Nanjing Bicbiotechnology Co., Ltd	58

N-Hydroxyurethane Spectrum

N-Hydroxyurethane(589-41-3)MS N-Hydroxyurethane(589-41-3)¹HNMR N-Hydroxyurethane(589-41-3)¹³CNMR N-Hydroxyurethane(589-41-3)IR1 N-Hydroxyurethane(589-41-3)Raman

589-41-3(N-Hydroxyurethane)Related 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

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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 ETHYL HYDROXYCARBAMATE ETHYL N-HYDROXYCARBAMATE HYDROXYCARBAMIC ACID ETHYL ESTER Ethylester kyseliny N-hydroxykarbaminove Ethyl Hydroxycarbamate Hydroxycarbamic Acid Ethyl Ester N-Hydroxyurethane ethylesterkyselinyn-hydroxykarbaminove hydroxy-carbamicaciethylester Hydroxyurethane N-Carbethoxyhydroxylamine NHU N-Hydroxy ethyl carbamate N-Hydroxyurethane> 85.0%(GC& 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)