N-PROPYLCARBAMATE
N-PROPYLCARBAMATE Basic information
- Product Name:
- N-PROPYLCARBAMATE
- Synonyms:
-
- propylcarbamate
- Propylester kyseliny karbaminove
- propylesterkyselinykarbaminove
- propylurethane
- TIMTEC-BB SBB000036
- CARBAMIC ACID-N-PROPYL ESTER
- Carbamic acid propyl
- n-Propylcarbamate (internal standard)
- CAS:
- 627-12-3
- MF:
- C4H9NO2
- MW:
- 103.12
- EINECS:
- 210-984-5
- Product Categories:
-
- Aliphatics
- Amines
- Metabolites & Impurities
- Mol File:
- 627-12-3.mol
N-PROPYLCARBAMATE Chemical Properties
- Melting point:
- 61-63 °C(lit.)
- Boiling point:
- 92-93 °C/12 mmHg(lit.)
- Density
- 0.9809 (estimate)
- refractive index
- 1.4228 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 13.54±0.50(Predicted)
- color
- White to Off-White
- Water Solubility
- 200.1g/L(37 ºC)
- IARC
- 3 (Vol. 12, Sup 7) 1987
- EPA Substance Registry System
- Propyl carbamate (627-12-3)
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26-36
- RTECS
- FD0875000
- HS Code
- 2924190090
- Hazardous Substances Data
- 627-12-3(Hazardous Substances Data)
N-PROPYLCARBAMATE Usage And Synthesis
Chemical Properties
White Solid
Uses
A metabolite of alkyl carbamate (ethyl or propyl).
Definition
ChEBI: N-Propyl carbamate is a carbamate ester.
Safety Profile
Moderately toxic by ingestion and subcutaneous routes. An experimental teratogen. Questionable carcinogen with experimental neoplas tigenic and tumorigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also CARBAMATES.
Synthesis
71-23-8
57-13-6
627-12-3
623-96-1
1. Catalyst preparation: The catalyst was prepared by calcining La(NO3)3-6H2O in air at 350 °C for 4 hours. 2. Preparation of reactants: 48.0 g of n-propanol, 6.0 g of urea, and 0.8 g (13.3% of the mass of urea) of the above-prepared catalyst were added to the autoclave. 3. Reaction conditions: The reaction was carried out at 180 °C for 6 h under autogenous pressure (ca. 12.2 atm). 4. 4. Product analysis: At the end of the reaction, the yields of dipropyl carbonate (DPC) and propyl carbamate (PC) were 54.2% by weight and 18.3% by weight, respectively.
References
[1] Patent: US2010/312001, 2010, A1. Location in patent: Page/Page column 3
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N-PROPYLCARBAMATE(627-12-3)Related Product Information
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