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1,3-dibutyl-1-nitrosourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56654-52-5

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56654-52-5 Usage

Type of compound

Nitrosourea derivative

Usage

Laboratory research as a mutagen and carcinogen

Toxicity

Known to be toxic

DNA interaction

Can cause damage to DNA

Consequences of DNA damage

Leading to mutations and potentially cancerous growths

Research applications

Studies on the mechanisms of cancer development and investigation of neurodegenerative diseases

Safety precautions

Proper safety precautions and handling procedures should be followed when working with this chemical

Check Digit Verification of cas no

The CAS Registry Mumber 56654-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,5 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56654-52:
(7*5)+(6*6)+(5*6)+(4*5)+(3*4)+(2*5)+(1*2)=145
145 % 10 = 5
So 56654-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H19N3O2/c1-3-5-7-10-9(13)12(11-14)8-6-4-2/h3-8H2,1-2H3,(H,10,13)

56654-52-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dibutyl-1-nitrosourea

1.2 Other means of identification

Product number -
Other names N-Nitroso-N,N'-dibutylharnstoff

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56654-52-5 SDS

56654-52-5Upstream product

56654-52-5Downstream Products

56654-52-5Relevant academic research and scientific papers

Kinetic study of the nitrosation of 1,3-dialkylureas in aqueous-perchloric acid medium

Gonzalez-Alatorre, Guillermo,Guzman-Maldonado, Salvador H.,Escamilla-Silva, Eleazar M.,Loarca-Pina, Guadalupe,Hernandez Benitez, Carlos

, p. 273 - 279 (2007/10/03)

The kinetics of the nitrosation of 1,3-dimethyl (DMU), 1,3-diethyl (DEU), 1,3-dipropylurea (DPU), 1,3-dibuthyl (DBU), and 1,3-diallylurea (DAU) were studied in a conventional UV/vis spectrophotometer in aqueous-perchloric acid media. The kinetic study was carried out using the initial rate method. The reaction rate observed was r = k[H+]2/[H+] + Ka [Diurea][Nitrite] where Ka is the acidity constant of nitrous acid. The diureas exhibited the reactivity order DMU ? DEU > DPU > DAU, which can be interpreted as a function of the steric impediment generated by the R alkyl group in the rate controlling step. A probable relationship between both the chemical reactivity and structure of the nitrosable substrate with the biological activity of the N-nitroso compounds generated is proposed.

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