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2-Hydroxyethyl 2-hydroxyethyl-carbamate, also known as HEHEC, is a colorless, odorless liquid with a slightly sweet taste and is soluble in water. It is a chemical compound commonly used as a preservative and antimicrobial agent in personal care products and industrial applications.
Used in Personal Care Products:
HEHEC is used as a preservative and antimicrobial agent in products such as shampoos and lotions for its effectiveness in inhibiting the growth of various microorganisms, including bacteria, yeast, and mold.
Used in Household Cleaners:
HEHEC is used as a preservative and antimicrobial agent in household cleaners for its ability to prevent the growth of bacteria, yeast, and mold, ensuring the cleanliness and safety of the products.
Used in Industrial Applications:
HEHEC is used as a preservative and antimicrobial agent in various industrial applications for its effectiveness in inhibiting the growth of microorganisms, contributing to the quality and safety of the products.

7506-80-1

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7506-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7506-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7506-80:
(6*7)+(5*5)+(4*0)+(3*6)+(2*8)+(1*0)=101
101 % 10 = 1
So 7506-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO4/c7-2-1-6-5(9)10-4-3-8/h7-8H,1-4H2,(H,6,9)

7506-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyethyl N-(2-hydroxyethyl)carbamate

1.2 Other means of identification

Product number -
Other names Thanol C 150

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:7506-80-1 SDS

7506-80-1Relevant academic research and scientific papers

Environment-friendly polyurethane chain extender as well as preparation method and application thereof

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Paragraph 0028-0038, (2020/04/22)

The invention relates to an environment-friendly polyurethane chain extender as well as a preparation method and application thereof, and belongs to the technical field of chemical materials. The compound is represented by the following formula I, wherein R1 is a straight chain or branched chain alkyl group consisting of C1-C6; and R2 is a straight chain or branched chain alkyl group consisting ofC1-C6. The environment-friendly polyurethane chain extender disclosed by the invention is applied to the preparation of a two-component polyurethane coating or adhesive. The environment-friendly chain extender has the beneficial effects that (1) the environment-friendly chain extender is a dibasic alcohol polyurethane chain extender containing carbamate, and the structure of the chain extender does not contain any aromatic group, so that the toxicity of the chain extender is greatly reduced; (2) relatively long operation time of the chain extender and the polyurethane material after mixing isensured; (3) the chain extender is high in strength and good in weather resistance after being cured, so that the performance of a polyurethane product can be improved, the application of the polyurethane product is enriched, and the diversified requirements of people on a polyurethane material are met.

Carbamate multi (methyl) acrylate as well as preparation method and application thereof (by machine translation)

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Paragraph 0037-0040, (2020/05/05)

The preparation method comprises the following steps (: reacting a cyclic carbonate with an organic amine to obtain the carbamate poly)-acrylic acid ester :S1. and reacting the cyclic carbonate with the organic amine, to prepare the radiation-curable urethane polyol ;S2. by catalyzing the ester exchange reaction or the esterification reaction (to prepare the radiation-curable urethane polymethacrylate) and the organic amine to prepare the urethane polyol (through catalyzing the transesterification reaction or the esterification reaction) to obtain the urethane polyalphamethyl (-acrylic acid ester, respectively). The preparation method comprises the following steps: catalyzing the ester exchange reaction or (the esterification reaction to obtain the carbamate polyalphamethyl-). acrylate; and, synthesizing, methyl, acrylic acid, The, preparation method comprises, the following steps: catalyzing the ester exchange reaction or the esterification reaction to obtain the carbamate polyol. (by machine translation)

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