Description

Ethyl dimethylcarbamate (CAS No. 687-48-9) is a high-purity organic compound with the molecular formula C₅H₁₁NO₂ and IUPAC name ethyl N,N-dimethylcarbamate. This versatile carbamate ester is synthesized under stringent quality control measures to ensure optimal purity and consistency, making it ideal for research and industrial applications. It appears as a clear, colorless liquid with a mild odor and is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. Ethyl dimethylcarbamate is widely utilized as a reagent in organic synthesis, pharmaceutical intermediates, and agrochemical development. Each batch undergoes rigorous analytical testing, including GC-MS and HPLC, to verify identity, purity, and absence of contaminants. Packaged in amber glass bottles or sealed drums to ensure stability, this product is designed for laboratory and bulk-scale use.

Properties

• CAS Number: 687-48-9
• Complexity: 80.5
• IUPAC Name: ethyl N,N-dimethylcarbamate
• InChI: InChI=1S/C5H11NO2/c1-4-8-5(7)6(2)3/h4H2,1-3H3
• InChI Key: SUDHEDJJFGYYPL-UHFFFAOYSA-N
• Exact Mass: 117.078978594
• Molecular Formula: C5H11NO2
• Molecular Weight: 117.15
• SMILES: CCOC(=O)N(C)C
• Topological: 29.5
• Monoisotopic Mass: 117.078978594
• Synonyms: ETHYL DIMETHYLCARBAMATE, Carbamic acid, N,N-dimethyl-, ethyl ester, 211-695-7, 687-48-9, Ethyl N,N-dimethylcarbamate, Dimethylethoxyformamide, Carbamic acid, dimethyl-, ethyl ester, N,N-Dimethylurethane, Dimethylcarbamic acid ethyl ester, Di-N-methyl ethyl carbamate, NSC-14090, Ethyldimethyl carbamate, Ethyl N,N-dimethyl carbamate, Ethyl N,N-dimethylcarbaminate, CCRIS 4092, EINECS 211-695-7, NSC 14090, BRN 1744697, dimethylurethane, dimethyl urethane, MFCD01738220, ETHYLDIMETHYLCARBAMATE, (CH3)2NCOOC2H5, 4-04-00-00222 (Beilstein Handbook Reference), MS4FB5752R, SCHEMBL1201195, SCHEMBL1415989, SCHEMBL1415992, SCHEMBL5780605, WLN: 2OVN1&1, C2H5OC(O)N(CH3)2, DTXSID40218829, NSC14090, AKOS006241752, AS-57876, DB-334312, CS-0112757, NS00036683, A10839, EN300-719460

Application

Ethyl dimethylcarbamate serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of carbamate-based drugs and prodrugs. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its reactivity as a carbamate derivative. Additionally, this compound finds use in organic chemistry as a protecting group or building block for more complex molecular architectures.

Safety and Hazards

GHS Hazard Statements

• H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
• H351 (100%): Suspected of causing cancer [Warning Carcinogenicity]

Precautionary Statements

• P203, P264, P270, P280, P301+P317, P318, P330, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (100%)
• Carc. 2 (100%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.