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Dihexyl hexane-1,6-diylbiscarbamate is a chemical compound with the molecular formula C20H38N2O4. It is an organic compound that belongs to the class of carbamates, which are derivatives of carbamic acid. This specific compound is characterized by its long-chain structure, with two hexyl groups (each containing six carbon atoms) attached to a central hexane-1,6-diyl moiety, which is connected to two carbamate groups. Dihexyl hexane-1,6-diylbiscarbamate is used as a plasticizer, a substance added to plastics to increase their flexibility, workability, or durability. It is particularly useful in the production of polyvinyl chloride (PVC) products due to its ability to enhance the plastic's properties without compromising its integrity. The compound is also known for its low volatility and resistance to extraction, making it a stable and effective additive in various industrial applications.

6271-27-8

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6271-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6271-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6271-27:
(6*6)+(5*2)+(4*7)+(3*1)+(2*2)+(1*7)=88
88 % 10 = 8
So 6271-27-8 is a valid CAS Registry Number.

6271-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name hexyl N-[6-(hexoxycarbonylamino)hexyl]carbamate

1.2 Other means of identification

Product number -
Other names N,N'-hexanediyl-bis-carbamic acid dihexyl ester

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:6271-27-8 SDS

6271-27-8Downstream Products

6271-27-8Relevant academic research and scientific papers

Visible-light photocatalyzed oxidative decarboxylation of oxamic acids: a green route to urethanes and ureas

Pawar, Govind Goroba,Robert, Frédéric,Grau, Etienne,Cramail, Henri,Landais, Yannick

supporting information, p. 9337 - 9340 (2018/08/31)

A sustainable metal-free route to urethanes and ureas based on a photocatalyzed oxidative decarboxylation of oxamic acids is described. The reaction includes in situ generation of an isocyanate from the oxamic acid, using an organic dye as a photocatalyst, a hypervalent iodine reagent as an oxidant and a light source, which trigger the free-radical decarboxylation. This protocol successfully avoids the isolation, purification and storage of carcinogenic isocyanates and allows elaboration of urethanes and ureas in a one-pot process from commercially available sources.

Method for Preparing Dicarbamate Compounds

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Paragraph 0032-0033; 0056-0057; 0067-0070, (2017/01/02)

The present invention provides a preparing method of dicarbamate, comprising: a first step of obtaining an alcohol solution including diureido obtained by reacting diamine having 2 to 13 carbon atoms with urea in the presence of alcohol having 3 to 12 carbon atoms at low temperature of 150anddeg;C or less; and a second step of obtaining dicarbamate by reacting the alcohol solution including the diureido at high temperature of 200anddeg;C or more under carbon dioxide pressure. According to the preparing method of the present invention, yield and selectivity of dicarbamate are significantly increased, and formation of an alkylated amine by-product can be minimized.COPYRIGHT KIPO 2016

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