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Dioctylnitrosoamine, also known as N-Nitroso-N-octyloctanamine, is a chemical compound with the molecular formula C16H34N2O. It is an organic nitrosoamine, which is a derivative of octylamine, and is characterized by the presence of a nitroso group (-N=O). Dioctylnitrosoamine is typically used as a fuel additive, specifically in diesel engines, to improve cetane numbers and enhance combustion efficiency. However, it is important to note that nitrosoamines, including dioctylnitrosoamine, are potentially harmful and can be carcinogenic, which means they have the ability to cause cancer. Due to these health risks, their use is strictly regulated, and they are subject to safety measures to minimize exposure.

6335-97-3

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6335-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6335-97-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6335-97:
(6*6)+(5*3)+(4*3)+(3*5)+(2*9)+(1*7)=103
103 % 10 = 3
So 6335-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H34N2O/c1-3-5-7-9-11-13-15-18(17-19)16-14-12-10-8-6-4-2/h3-16H2,1-2H3

6335-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dioctylnitrous amide

1.2 Other means of identification

Product number -
Other names N-Dioctylnitrosamine

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:6335-97-3 SDS

6335-97-3Downstream Products

6335-97-3Relevant academic research and scientific papers

Oxone-sodium nitrite mediated N-nitrosamines formation under mild conditions from secondary amines

Gaur, Pinki,Banerjee, Shaibal

, p. 2270 - 2279 (2019/07/03)

Herein, we report an efficient synthesis of N-nitrosamines from cyclic, aliphatic, benzylic, and aromatic secondary amines via a novel straightforward, efficient, and mild chemical process using sodium nitrite and Oxone in methanol as a solvent at 0–5 °C. The demonstrated methodology accounts well for the parameters like cost-effective, short reaction time, clean and safe handling along with good to excellent yields.

Iodide-catalyzed synthesis of N-nitrosamines via C-N cleavage of nitromethane

Zhang, Jie,Jiang, Jiewen,Li, Yuling,Wan, Xiaobing

, p. 11366 - 11372 (2013/12/04)

An iodide-catalyzed process to synthesize N-nitrosamines has been developed using TBHP as the oxidant. The mild catalytic system succeeded in cleaving the carbon-nitrogen bond in nitromethane. This methodology uses commercially available, inexpensive catalysts and oxidants and has a wide substrate scope and operational simplicity.

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