35601-81-1

Basic information

• Product Name: isopropyl ethylcarbamate
• Synonyms: isopropyl ethylcarbamate;Ethylcarbamic acid 1-methylethyl ester
• CAS NO: 35601-81-1
• Molecular Formula: C6H13NO2
• Molecular Weight: 131.17292
• EINECS: 252-636-5
• Mol File: 35601-81-1.mol

Chemical Properties

• Boiling Point: 183.8°Cat760mmHg
• Flash Point: 65°C
• Appearance: /
• Density: 0.935g/cm³
• Vapor Pressure: 0.756mmHg at 25°C
• Refractive Index: 1.415
• CAS DataBase Reference: isopropyl ethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: isopropyl ethylcarbamate(35601-81-1)
• EPA Substance Registry System: isopropyl ethylcarbamate(35601-81-1)

Safety Data

• Hazardous Substances Data: 35601-81-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Isopropyl ethylcarbamate is used as an anthelmintic drug for the treatment of parasitic infections, specifically targeting filariasis. It works by paralyzing and killing the worms, thereby reducing the symptoms and complications associated with the infection.
Used in Insect Repellent Industry:
As an insect repellent, isopropyl ethylcarbamate is used to deter insects and protect against bites that may transmit diseases or cause discomfort.
Used in Cosmetics and Personal Care Products:
Isopropyl ethylcarbamate is used as a preservative in cosmetics and personal care products to maintain their freshness and prevent spoilage, ensuring the safety and efficacy of these products for consumers.
Used in Topical Medications:
Isopropyl ethylcarbamate is used as an active ingredient in topical medications to provide relief from itching, which can be caused by various skin conditions or insect bites. Its effectiveness in alleviating itching contributes to the overall comfort and well-being of individuals using these medications.

InChI:InChI=1/C6H13NO2/c1-4-7-6(8)9-5(2)3/h5H,4H2,1-3H3,(H,7,8)

Upstream product

• 67-63-0 isopropyl alcohol 
• 109-90-0 ethyl isocyanate 
• 75-04-7 ethylamine 
• 74305-11-6 C₅H₁₀N₂O₄ 

Relevant articles and documents

Removal of flotation collector O-isopropyl-N-ethylthionocarbamate from wastewater

Flotation collector O-isopropyl N-ethylthionocarbamate (IPETC) is widely used for separation of sulfide ores. Its removal from water by several oxidation processes was studied. Photocatalytic oxidation with air in the presence of iron salts, utilizing solar irradiation or artificial UV-A light is very efficient. Oxidation leads through the formation of O-isopropyl N-ethylcarbamate and several other reaction intermediates to total decomposition of organic compound in the final stage in 1 day. Similar results were obtained with a Fenton type oxidation with hydrogen peroxide and iron salts. Treatment with sodium hypochlorite yields mainly O-isopropyl N-ethylcarbamate. The formation of this compound in wastewaters can be of concern, since simple alkyl carbamates are cancer suspect agents.

Continuous Flow Synthesis of Urea-Containing Compound Libraries Based on the Piperidin-4-one Scaffold

The advantages of performing reactions in continuous flow vs. the classic batch processes render flow chemistry a suitable technique for library synthesis. Inspired by our recent work to create fluorine-containing nitrogen heterocycles and by the potentia

Nucleophilic Substitutions to Carbonic Acid Derivates. XII. Kinetics and Mechanism of the Reaction of N-Nitro-N-alkyl-urethanes with Primary Aliphatic Amines

The aminolysis of N-alkyl-N-nitrourethanes takes place, as the kinetical studies demonstrate, by means of several consecutive steps.The nucleophilic attack of the amine (first step; reaction B), as well as the proton-transfere (second step; reaction C), are quick pre-equilibres, followed by the slow, rate-determining elimination of the nitramino-group (reaction D).During the deprotonation, an intermediate with two to the nitramino-group antiperiplanar orbitals is formed, providing the necessary mesomeric assistance of the elimination.