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Carbamic acid

Carbamic acid, also known as aminoformic acid, is the simplest organic compound in the class of carbamic acids, characterized by the molecular formula CH₃NO₂ (or NH₂COOH), where a hydrogen atom in ammonia is replaced by a carboxy group.^[1] It features a structure with a carboxyl group directly bonded to an amino group, making it the parent compound of carbamates and analogous to carbonic acid in its functional group arrangement.^[2] With a molecular weight of 61.04 g/mol, it is a one-carbon metabolite observed in biological systems such as Escherichia coli, though it exists primarily as the conjugate base carbamate rather than the free acid.^[1] Despite its structural simplicity, carbamic acid is highly unstable under standard conditions and cannot be isolated or synthesized in pure form, readily decomposing into ammonia (NH₃) and carbon dioxide (CO₂).^[2] This instability arises from the weak C–N bond and the tendency to revert to its precursor components, similar to the decomposition of carbonic acid, preventing direct esterification to form carbamates.^[2] In specialized environments, such as low-temperature interstellar ices formed from ammonia and carbon dioxide mixtures, carbamic acid and its dimer can persist up to 290 K before subliming or decomposing.^[3] Carbamic acid holds significant chemical and biochemical importance as the foundational species for carbamate derivatives, which are esters widely applied in agriculture as insecticides (e.g., N-methylcarbamates) and herbicides due to their selective toxicity and biodegradability via hydrolysis.^[2] These derivatives also serve as intermediates in the synthesis of polyurethanes, versatile polymers used in foams, coatings, and insulation materials produced from diisocyanates and diols.^[2] In biological contexts, carbamic acid intermediates facilitate CO₂ capture and transport in amine-based systems, underscoring its role in metabolic pathways despite its transient nature.^[1]

Properties

Physical properties

Carbamic acid has the molecular formula H₂NCO₂H (also written as NH₂COOH) and a molar mass of 61.040 g/mol.^[1] In the solid state at low temperatures, it exists as a white solid that forms dimers linked by hydrogen bonds between the carboxylic acid moieties.^[4]^[5] The compound exhibits thermal stability up to approximately 280 K (−93 °C) for the monomer and 290 K for the dimer, above which it decomposes into ammonia and carbon dioxide or sublimes.^[4] Due to this instability at room temperature, carbamic acid lacks distinct melting or boiling points and instead undergoes sublimation around 280 K.^[4] It is highly soluble in water, with a computed solubility of approximately 379 g/L attributed to its polar structure, though experimental data on solubility in organic solvents remains limited.^[6]

Chemical properties

Carbamic acid exhibits significant instability, undergoing endothermic decomposition into ammonia and carbon dioxide above approximately 280 K via the reaction

\mathrm{H_2NCO_2H \rightarrow NH_3 + CO_2}

with a gas-phase activation barrier of 149 kJ/mol, though solvation in icy environments lowers this barrier and accelerates the process.^[4] This thermal decomposition highlights its fleeting nature in condensed phases, where it persists only up to approximately 280 K before subliming or dissociating.^[4] As a weak acid, carbamic acid has computed pKa values ranging from 3.9 to 5.9, enabling the formation of salts such as ammonium carbamate upon deprotonation.^[6]^[7] Recent studies indicate that, unlike some early reports suggesting a zwitterionic form, carbamic acid exists primarily in its neutral form (H₂NCOOH) in low-temperature solids and ices, stabilized by hydrogen bonding, though the zwitterionic form (H₃N⁺COO⁻) is thermodynamically unstable and decomposes rapidly in isolation. In aqueous solutions, carbamic acid readily undergoes hydrolysis, often via alkaline pathways that yield bicarbonate species, underscoring its role as a transient intermediate in carbon dioxide fixation reactions, such as those in amine-promoted CO₂ capture systems.^[8] This reactivity stems from nucleophilic attack by water or hydroxide on the carbonyl group, facilitating conversion to more stable products. Infrared spectroscopy provides key insights into its functional groups, revealing characteristic absorptions including N-H stretches near 3400 cm⁻¹, a C=O stretch at approximately 1700 cm⁻¹ (specifically 1698 cm⁻¹ in ices) indicative of the neutral carbamoyl moiety, and O-H stretches around 3000 cm⁻¹, though these features are complicated by hydrogen bonding in solid or solvated states.^[9]^[4]

Structure

Carbamic acid has the molecular formula \ce{NH2CO2H} or \ce{CH3NO2}, consisting of an amino group (\ce{-NH2}) directly bonded to a carboxyl group (\ce{-COOH}). The central carbon atom is bonded to the nitrogen, a double-bonded oxygen (\ce{C=O}), and a hydroxyl group (\ce{-OH}), resulting in a structure analogous to carbonic acid but with one \ce{OH} replaced by \ce{NH2}. The molecule is generally planar, with the amino group exhibiting some pyramidal character due to the sp³ hybridization of nitrogen, though computational studies indicate partial conjugation leading to near-planarity.^[3] Due to its instability, experimental structural data are limited, and parameters are primarily derived from quantum chemical calculations. For instance, at the B3LYP/cc-pVTZ level in the gas phase, the \ce{C=O} bond length is 1.21 Å and the \ce{C-O} (single) bond is 1.36 Å, comparable to those in acetic acid.^[3] Carbamic acid can also exist in a zwitterionic form, \ce{^+H3N-COO^-}, particularly in low-temperature environments or computational models, where the proton transfers from the carboxyl to the amino group; this form is highly unstable and readily decomposes to \ce{NH3} and \ce{CO2}.^[10]

Discovery and synthesis

Historical aspects

The term "carbamic acid" was first recorded between 1860 and 1865, derived from the combination of "carb-" (referring to carbon) and "amide," reflecting its conceptual origin as a urea derivative. It was initially described as a hypothetical parent compound underlying the structure of carbamates, which are esters or salts derived from this unstable acid.^[11]^[12] Early recognition of compounds related to carbamic acid emerged in the 19th century through observations of natural extracts, particularly from the Calabar bean (Physostigma venenosum), used traditionally as an ordeal poison in West Africa. Western documentation began in 1846 when the bean's effects were noted, leading to the isolation of physostigmine—a methyl carbamate—in 1864 by chemists Jobst and Hesse. This discovery highlighted carbamate structures in natural alkaloids, prompting further chemical exploration.^[13]^[14]^[15] Formal identification of carbamic acid itself built on the known reaction between ammonia and carbon dioxide, which forms ammonium carbamate as a stable salt; this reaction was empirically observed in the early 19th century, but the acid was proposed as an intermediate in the 1870s during studies of urea formation. In the context of urea synthesis, Justus von Liebig, collaborating with Friedrich Wöhler in the 1830s, analyzed urine constituents and degradation products, including urea, leading to early 20th-century proposals viewing carbamic acid as a key intermediate in biochemical pathways related to urea.^[16]^[17] Pre-1950 developments included initial spectroscopic studies in the 1940s that confirmed structural features in carbamic acid derivatives, such as ethyl carbamate, using emerging infrared techniques to probe amidic bonds. However, the acid's instability prevented commercial isolation until low-temperature methods in the late 20th century enabled its preparation and characterization as a solid at low temperatures, marking a milestone in direct characterization. These historical insights also underscored carbamic acid's role as an intermediate in urea production processes.^[18]^[19]

Synthesis methods

Carbamic acid is primarily synthesized in the laboratory through the direct reaction of ammonia and carbon dioxide at low temperatures, typically below 250 K, where the exothermic addition forms the solid compound in equilibrium with ammonium carbamate. The reaction proceeds via nucleophilic addition: \ce{NH3 + CO2 -> H2NCO2H}, and a subsequent proton transfer with additional ammonia yields \ce{[NH4+][H2NCO2^-]}. This method, adapted from interstellar ice simulations, efficiently produces carbamic acid and ammonium carbamate in a 1:1 ratio above 80 K, with the acid persisting up to approximately 280 K before decomposition begins.^[4] For substituted carbamic acids, a similar approach involves bubbling carbon dioxide through solutions of secondary amines (R₂NH) at low temperatures, often in solvents like methanol, to form RR′NCO₂H as solids or precipitates. This direct carboxylation occurs at ambient or mildly reduced temperatures and low CO₂ pressures, with complete conversion of the amine achievable in pure or dilute solutions. For example, diamines yield solid carbamic acids quantitatively under a CO₂ flow at room temperature.^[20]^[21] An alternative historical route, though hazardous due to the toxicity of phosgene, involves reacting ammonia with phosgene to form carbamoyl chloride (\ce{H2NCOCl}) at high temperatures around 400–500 °C, followed by careful hydrolysis with water to generate carbamic acid. This method achieves high yields for the chloride intermediate (90–95%) but is largely supplanted by safer CO₂-based processes.^[22]^[23] Modern catalytic methods for CO₂ fixation enhance efficiency, particularly for substituted variants. Tin alkoxides, such as organotin(IV) dimethoxides, catalyze the reaction of amines with CO₂ to form carbamates as stable precursors to carbamic acids, with yields up to 92% under mild conditions (e.g., 100–150 °C, 10–20 bar). Transition-metal-free protocols, including those using superbases or ionic liquids, enable direct synthesis from amines and CO₂ under pressure (e.g., 1–5 MPa at 50–100 °C), avoiding metal contaminants and achieving good selectivity for carbamic acid derivatives.^[24]^[25] On an industrial scale, carbamic acid serves as a transient intermediate in the Bosch-Meiser urea process, where ammonia and carbon dioxide react at 170–220 °C and 12.5–25 MPa to form ammonium carbamate, which dehydrates to urea (\ce{H2NCO2H + NH3 -> [NH4][H2NCO2] -> (NH2)2CO + H2O}). Single-pass conversion to the carbamate stage is high, but single-pass conversion to urea is typically around 50-70% due to equilibrium limitations in dehydration, necessitating recycling. Purification of carbamic acid remains challenging owing to its volatility and tendency to decompose back to NH₃ and CO₂ above -50 °C.^[26]^[27]

Derivatives

Substituted carbamic acids

Substituted carbamic acids are compounds of the general formula RR′NCO₂H, where R and R′ represent alkyl or aryl groups.^[28] These include N-monosubstituted derivatives, such as methylcarbamic acid (CH₃NHCO₂H), formed from primary amines, and N,N-disubstituted derivatives from secondary amines.^[29] These acids are synthesized directly by the reaction of amines with carbon dioxide under mild conditions, often at ambient temperature and pressure in non-aqueous solvents.^[30] The mechanism involves nucleophilic attack by the amine on CO₂, facilitated by a second amine molecule or water through a concerted six-membered transition state, with an activation energy of approximately 13 kcal/mol for methylamine.^[30] Unlike the parent carbamic acid, which decomposes above 230 K, substituted variants exhibit somewhat greater stability in polar solvents due to hydrogen bonding, though they remain transient species.^[29] Substituted carbamic acids are generally unstable and decompose via decarboxylation to the corresponding amine and CO₂, particularly in aqueous media.^[2] Most cannot be isolated as solids at room temperature and are characterized under cryogenic conditions or in matrix isolation experiments; for example, neutral methylcarbamic acid has been characterized in matrix isolation experiments as forming stable dimers that persist up to 260 K, although the associated ionic precursor decomposes above 230 K.^[29] Electron-withdrawing groups on the substituents can enhance acidity by stabilizing the conjugate base, analogous to effects in related carboxylic acids, though quantitative data for carbamic acids is limited.^[31] In organic synthesis, these acids serve as reactive intermediates, often generated in situ for the preparation of carbamates and ureas without isolation.^[32] They find utility as precursors in pharmaceutical synthesis, where their transient nature allows controlled functionalization before decomposition.^[32]

Carbamate esters

Carbamate esters, with the general formula \ce{RR'NCO2R''} where R, R', and R'' are typically alkyl or aryl groups, represent stable derivatives of carbamic acid in which the acidic proton is replaced by an alkoxy or aryloxy group.^[33] These compounds combine amide-like and ester-like characteristics due to resonance stabilization between the nitrogen lone pair and the carbonyl group, resulting in a planar structure around the C-N-C-O moiety.^[34] Representative examples include ethyl carbamate (\ce{H2NCO2CH2CH3}), also known as urethane, and methyl carbamate (\ce{H2NCO2CH3}), both of which are white crystalline solids at room temperature.^[35] Synthesis of carbamate esters commonly proceeds via alcoholysis of isocyanates, where an isocyanate (\ce{RNCO}) reacts with an alcohol (\ce{R''OH}) to yield the carbamate (\ce{RNHCO2R''}) under mild conditions, often catalyzed by bases or metal salts to facilitate nucleophilic addition.^[33] Another key route involves the reaction of chloroformates (\ce{R''OC(O)Cl}) with amines (\ce{RR'NH}), producing the carbamate (\ce{RR'NCO2R''}) and HCl, typically in the presence of a base like triethylamine or cesium carbonate to neutralize the acid byproduct; this method is versatile for incorporating diverse substituents and can be optimized with catalysts such as indium for improved yields and selectivity in multifunctional substrates.^[34] Additionally, carbamate esters are accessible through the Curtius or Hofmann rearrangements, in which acyl azides or bromoamides are converted to isocyanates under thermal or chemical activation, followed by trapping with alcohols to form the ester directly.^[33] Carbamate esters exhibit good chemical stability at room temperature, resisting hydrolysis under neutral conditions and maintaining integrity during storage or processing, which contrasts with the instability of the parent carbamic acid.^[35] However, ethyl carbamate demonstrates carcinogenic potential, classified as a probable human carcinogen based on sufficient evidence from animal studies showing tumors in multiple organs, leading to restrictions in its industrial and pharmaceutical uses.^[35] In infrared spectroscopy, the carbonyl stretching frequency appears as a strong absorption around 1700 cm⁻¹, shifted lower than typical esters (1735–1750 cm⁻¹) due to the electron-donating nitrogen resonance that weakens the C=O bond.^[36] Reactivity of carbamate esters includes base- or enzyme-catalyzed hydrolysis, which cleaves the ester linkage to regenerate the amine (\ce{RR'NH}), alcohol (\ce{R''OH}), and carbon dioxide (\ce{CO2}), with rates influenced by the leaving group and substitution on nitrogen.^[33] This hydrolysis serves as a protective strategy in synthesis but also limits their persistence in biological environments. Carbamate esters play a crucial role as precursors in polymer chemistry, particularly in the formation of polyurethanes through stepwise reaction of diisocyanates with diols, yielding linear or crosslinked networks with the repeating urethane linkage.^[33] Ethyl carbamate was first synthesized in the mid-19th century, with Charles-Adolphe Wurtz reporting its preparation in 1848–1849 via the reaction of ethanol with cyanic acid or related precursors, marking an early milestone in organic ester chemistry.^[37] Due to its carcinogenic properties, its application has since been curtailed in many contexts, though it remains a model compound for studying carbamate behavior.^[35]

Occurrence

Biological occurrence

Carbamic acid plays a transient role as an intermediate in the urea cycle of mammals, where it is formed during the synthesis of carbamoyl phosphate by carbamoyl phosphate synthetase I (CPSI). In this enzymatic process, bicarbonate is first activated by ATP to form carboxyphosphate, which then reacts with ammonia to generate carbamate (the deprotonated form of carbamic acid, H₂NCOO⁻); this intermediate is subsequently phosphorylated by a second ATP molecule to yield carbamoyl phosphate (H₂NCOOPO₃²⁻), which enters the ornithine transcarbamylase-catalyzed step to produce citrulline.^[38] The reaction can be approximated as NH₃ + CO₂ + ATP → H₂NCO₂H + ADP + Pᵢ, though the full cycle consumes two ATP equivalents and ensures rapid conversion to prevent accumulation.^[39] This step is crucial for detoxifying ammonia in the liver mitochondria, maintaining nitrogen homeostasis. In bacterial metabolism, carbamic acid derivatives are involved in CO₂ fixation and nitrogen assimilation pathways, particularly through the action of carbamate kinase. This enzyme catalyzes the reversible phosphorylation of carbamate to carbamoyl phosphate using ATP (carbamate + ATP ⇌ carbamoyl-P + ADP), where carbamate arises from the non-enzymatic equilibrium of NH₃ and CO₂ (NH₃ + CO₂ ⇌ H₂NCO₂H ⇌ H₂NCOO⁻ + H⁺).^[40] In organisms like Escherichia coli and hyperthermophilic archaea, this facilitates the incorporation of inorganic carbon and nitrogen into organic compounds, such as during arginine biosynthesis or anaerobic energy generation from allantoin degradation.^[41] These processes highlight carbamic acid's utility in microbial adaptation to nitrogen-limited environments. A key biological function of carbamic acid occurs in CO₂ transport within vertebrate blood, where it forms carbaminohemoglobin through binding to the N-terminal amino groups of deoxygenated hemoglobin (Hb-NH₂ + CO₂ → Hb-NH-CO₂H → Hb-NH-COO⁻ + H⁺). This carbamate derivative accounts for approximately 20% of total CO₂ carriage from tissues to lungs, enhancing the Bohr effect by promoting oxygen release.^[42] The binding is favored in deoxygenated states, with up to 0.7–1 mol CO₂ per mol hemoglobin tetramer, underscoring its physiological significance in gas exchange.^[43] Due to its instability in aqueous environments (spontaneous decomposition to NH₃ and CO₂ with a half-life of seconds at physiological pH), carbamic acid exists at trace concentrations (<1 μM) in biological fluids such as blood plasma and cellular compartments, where it is rapidly converted to urea, bicarbonate, or other metabolites.^[44] In evolutionary contexts, carbamic acid is considered a potential prebiotic precursor in amino acid synthesis, as it can serve as a building block for more complex proteinogenic amino acids under primitive Earth conditions, linking simple gases like NH₃ and CO₂ to biogenic molecules.^[4]

Astrophysical occurrence

Ammonium carbamate, a salt derived from carbamic acid, has been tentatively identified in astrophysical environments through infrared spectroscopy of interstellar ices. In a 2025 study utilizing the James Webb Space Telescope (JWST) with the NIRSpec instrument, spectral signatures attributed to ammonium carbamate (NH₄⁺NH₂COO⁻) were observed in the protoplanetary disk d216-0939, located in the Orion Nebula Cluster. These observations, combined with Mid-Infrared Instrument (MIRI) data, revealed features in the 2.8–4.0 μm and 5.6–8 μm wavelength ranges, matching laboratory spectra of UV-irradiated CO₂ + NH₃ ice mixtures heated to 230 K.^[45] Key observational evidence includes characteristic infrared absorption bands, such as the N-H stretching mode at approximately 3300 cm⁻¹ and the C=O stretching mode at around 1700 cm⁻¹, consistent with ammonium carbamate in ice matrices within protostellar disks and molecular clouds. Laboratory simulations indicate that carbamic acid forms in these environments via irradiation of ammonia (NH₃) and carbon dioxide (CO₂) ices at temperatures of 10–20 K, typical of dense interstellar regions. Its abundance is estimated to be on the order of 10⁻⁶ relative to water ice, based on modeled ice compositions in such settings.^[46]^[4] A 2023 study from the University of Hawaii at Mānoa provided further confirmation through lab-based simulations of interstellar ices, demonstrating thermal synthesis of carbamic acid and its dimer from NH₃–CO₂ mixtures deposited at low temperatures and gradually heated. The dimer remains stable up to 290 K, suggesting persistence near young stellar objects where it could serve as a feedstock for complex molecules on cosmic dust grains. These findings imply that carbamic acid's origins predate Earth's formation, potentially arising in stellar nurseries.^[4] Carbamic acid, sometimes considered the simplest amino acid, holds prebiotic significance in astrochemistry, acting as a potential building block for more complex amino acids through dimerization and further reactions in interstellar ices. Its detection supports hypotheses of panspermia, wherein life's molecular precursors could be transported to habitable planets via comets and meteorites from these cosmic environments.^[4]^[47]

Applications

Industrial applications

Carbamic acid is not employed directly in industrial processes owing to its inherent instability and tendency to decompose into ammonia, carbon dioxide, and water. Instead, its derivatives, such as ammonium carbamate, play crucial roles as intermediates in large-scale manufacturing.^[48] The foremost application involves urea production through the Bosch-Meiser process, in which ammonia and carbon dioxide react under high pressure and temperature to form ammonium carbamate as a key intermediate, followed by dehydration to yield urea: \ce{NH3 + CO2 -> NH2COONH4 -> (NH2)2CO + H2O}. This process accounts for the bulk of industrial activity related to carbamic derivatives, with global urea output surpassing 180 million metric tons annually and accounting for approximately 55% of nitrogen-based fertilizer production (as of 2024).^[49]^[50]^[51]^[52] Carbamate esters derived from carbamic acid serve as essential monomers or linkages in polyurethane synthesis, enabling the production of versatile materials like flexible foams, rigid foams, coatings, and adhesives via reaction with polyols and isocyanates. The global polyurethane market exceeds $80 billion in value each year, underscoring the economic scale of these applications.^[53]^[54] In carbon dioxide capture and sequestration, carbamate formation occurs transiently during amine scrubbing, where primary or secondary amines such as monoethanolamine react with CO₂ to generate carbamates: \ce{2 R-NH2 + CO2 -> R-NH-COONH-R}, facilitating CO₂ absorption before regeneration. This mechanism is central to post-combustion capture in power plants and industrial emissions control.^[55]^[56] Carbamic acid derivatives also function as intermediates in the synthesis of certain herbicides, contributing to the development of carbamate-based compounds for weed control in agriculture.^[57]

Pharmaceutical applications

Carbamate derivatives of carbamic acid play a significant role in pharmaceutical applications, particularly as central nervous system (CNS) agents and in targeted cancer therapies, due to their ability to modulate neurotransmitter systems and exhibit favorable pharmacokinetic profiles. These compounds often function as prodrugs or direct active agents, leveraging the carbamate group's hydrolytic stability for oral bioavailability and controlled release in vivo.^[58] In the category of muscle relaxants and anxiolytics, emylcamate (ethyl methylcarbamate) has been utilized for treating anxiety and muscle spasms by enhancing the inhibitory effects of gamma-aminobutyric acid (GABA) at GABA-A receptors, thereby reducing neuronal excitability in the CNS. This mechanism promotes relaxation without the sedative potency of barbiturates, though its use has declined in favor of newer agents.^[59]^[60] As anticonvulsants, felbamate, a dicarbamate derivative, is approved for refractory epilepsy, particularly partial seizures and Lennox-Gastaut syndrome in children, through dual mechanisms involving blockade of N-methyl-D-aspartate (NMDA) receptors to limit excitotoxicity and enhancement of GABA-mediated inhibition. Despite its efficacy, felbamate's clinical application is restricted due to rare but serious risks of aplastic anemia and hepatic failure, necessitating careful monitoring.^[61]^[62] Beyond CNS applications, carbamate motifs appear in chemotherapeutic agents, such as platinum(IV) complexes bearing axial carbamate ligands, which serve as prodrugs for platinum(II) anticancer drugs like cisplatin analogs. These complexes exhibit improved stability, reduced nephrotoxicity, and enhanced tumor targeting via ligand reduction in hypoxic cancer environments, showing promising cytotoxicity in preclinical models against various solid tumors. Historically, ethyl carbamate (urethane) was employed as an intravenous anesthetic in the mid-20th century but was discontinued due to its carcinogenic potential, linked to DNA damage and tumor induction in animal studies.^[63]^[64]^[65] Pharmacologically, carbamates demonstrate rapid in vivo hydrolysis via esterases, yielding the parent amine, alcohol, and carbon dioxide, which contributes to their short duration of action and generally low toxicity profile compared to organophosphates. Unlike organophosphates, which cause irreversible acetylcholinesterase inhibition leading to prolonged cholinergic crisis, carbamates form reversible carbamylated enzyme intermediates that spontaneously decarbamylate within hours, resulting in milder, self-limiting toxicity. Carbamate-based drugs represent a modest fraction of CNS therapeutics, with established agents like felbamate and rivastigmine comprising part of the portfolio for epilepsy and dementia; however, no new approvals for simple carbamate structures have occurred post-2020, with research shifting toward hybrid carbamate scaffolds for improved selectivity and reduced side effects.^[33]^[66]^[58]

Pesticidal applications

Carbamate esters serve as key active ingredients in insecticides, primarily functioning as inhibitors of the enzyme acetylcholinesterase (AChE) in target pests. This inhibition disrupts nerve impulse transmission by preventing the breakdown of acetylcholine, leading to overstimulation and paralysis. Unlike organophosphate insecticides, which form a stable, irreversible bond with AChE, carbamates produce a carbamylated enzyme complex that spontaneously hydrolyzes, resulting in reversible inhibition and potentially lower persistence in biological systems.^[67] Prominent examples include carbaryl (1-naphthyl methylcarbamate), widely applied against aphids and other chewing insects on crops such as fruits, vegetables, and ornamentals, with global annual production on the order of 10,000 tonnes. Similarly, aldicarb acts as a systemic insecticide targeting soil-dwelling pests and aphids through the same AChE inhibition mechanism, though its high potency has led to phased restrictions in many regions.^[68]^[69]^[70] In herbicide applications, carbamate derivatives like phenmedipham are used post-emergence for broadleaf weed control in sugar beet crops. Phenmedipham inhibits photosynthesis by blocking electron transport in photosystem II, with selectivity achieved through differences in plant enzyme metabolism; sugar beets rapidly degrade the compound via hydroxylation and conjugation, minimizing phytotoxicity, while susceptible weeds lack this efficiency.^[71]^[72] The development of carbamate pesticides surged post-World War II, building on wartime research into nerve agents, with the first commercial insecticide, carbaryl, introduced in 1956 amid expanding agricultural demands. This era marked a shift from inorganic compounds to synthetics, enabling broader pest control but raising long-term ecological questions.^[73]^[74] Environmental concerns with carbamate pesticides include risks to non-target pollinators, prompting ongoing environmental concerns and calls for restrictions in the European Union to mitigate bee exposure and colony declines. Bioaccumulation is generally low due to their moderate lipophilicity and rapid metabolism in organisms, contrasting with more persistent organochlorines. In soil, half-lives typically range from 1 to 30 days under aerobic conditions, influenced by microbial degradation and temperature, though variability exists based on formulation and application rates. Recent 2024 reviews emphasize sustainable alternatives, such as biopesticides and integrated pest management, to reduce reliance on carbamates while maintaining crop yields.^[75]^[76]^[77]

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3); and finally carbamate interacts with the second molecule of ATP in a carbamate kinase reaction to yield CP (Eq. 4).
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The carbamate kinase-like carbamoyl phosphate synthetase ... - PNAS
The gene coding for this CK-like CPS was called cpkA. Carbamoyl phosphate (CP) is a key metabolite in nitrogen metabolism because it is a precursor of both ...
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Carbon Dioxide Transport | Anesthesiology Core Review
Hemoglobin possesses four N-terminal amino groups, each of which can bind CO2 to form carbaminohemoglobin. During the reaction, a proton is released, which ...
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A JWST investigation of the highly inclined disk d216-0939
The detection of molecules in planet-forming disks provides a bridge between the chemical evolution of the interstellar medium (ISM) and chemistries of planets ...
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Carbamic acid produced by the UV/EUV irradiation of interstellar ice ...
We have carried out irradiations of ice mixtures containing H 2 O, 12 CO 2 / 13 CO 2 and NH 3 with ultraviolet (UV)/extreme ultraviolet (EUV) photons.Missing: abundance | Show results with:abundance
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Interstellar ices could have been the nursery for building blocks of life
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Carbamic Acid - an overview | ScienceDirect Topics
Carbamic acid is an organic compound, the monoamide of carbon dioxide, from which carbamates are derived, and is the underlying structure of carbamates.
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Modeling the synthesis section of an industrial urea plant
Urea production consists of two reactions. In the first reaction, ammonia and carbon dioxide react to form ammonium carbamate which decomposes to urea and water ...
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Urea Market Size, Share & Trend, Analysis Graph Report By 2033
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[PDF] Ammonia and Urea Production
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Synthesis of organic carbamates as polyurethane raw materials from ...
We also present a practical and environmentally friendly method for the highly efficient synthesis of various organic carbamates, including industrially ...
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Jul 28, 2025 · The Polyurethane Market is expected to reach USD 87.48 billion in 2025 and grow at a CAGR of 5.36% to reach USD 113.84 billion by 2030.
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Mechanistic insights into carbamate formation from CO2 and amines
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Thermodynamic analysis of carbamate formation and carbon ...
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Carbamic Acid Derivative - an overview | ScienceDirect Topics
The N-methyl esters of carbamic acid are insecticides. Other derivatives of carbamic, thiocarbamic, and dithiocarbamic acids are herbicides and fungicides.
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The research of carbamates as potential drugs began with the discovery of physostigmine, a methyl carbamate ester isolated in pure form from the seeds of ...
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Jun 23, 2017 · The therapeutic efficacy of Emylcamate can be increased when used in combination with Magnesium sulfate. The risk or severity of CNS depression ...
[52]
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Felbamate - StatPearls - NCBI Bookshelf - NIH
Jul 6, 2025 · Mechanism of Action ... Absorption: Felbamate is well absorbed from the gastrointestinal (GI) tract, with oral bioavailability exceeding 90%. Peak ...Continuing Education Activity · Indications · Mechanism of Action · Contraindications
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Synthesis, Characterization, and Cytotoxicity of Platinum(IV ...
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[56]
Hazards of urethane (ethyl carbamate): a review of the literature
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[57]
Urethan - an overview | ScienceDirect Topics
Urethane was once used as an anesthetic in veterinary medicine. Its veterinary use was discontinued in 1948 when its carcinogenic properties were revealed. View ...
[58]
Carbamate Toxicity - StatPearls - NCBI Bookshelf
Carbamates are a class of insecticides structurally and mechanistically similar to organophosphate (OP) insecticides. Carbamates are N-methyl carbamates derived ...Continuing Education Activity · Introduction · Toxicokinetics · Differential Diagnosis<|separator|>
[59]
Mechanism of action of organophosphorus and carbamate ... - NIH
Organophosphorus and carbamate insecticides are toxic to insects and mammals by virtue of their ability to inactivate the enzyme acetylcholinesterase.
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Carbaryl (EHC 153, 1994) - Inchem.org
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Aspects of Pesticidal Uses of Carbaryl on Man and the Environment
On June 9 of the second year, insecticide appli- cation was made and sampling continued. ... Sevin carbaryl insecticide has been used worldwide since 1959 for ...Missing: global | Show results with:global
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The toxicologic effects of the carbamate insecticide aldicarb in ... - NIH
The primary mechanism of toxic action of aldicarb is cholinesterase inhibition. However, unlike the relatively irreversible anticholinesterase activity of the ...
[63]
Herbicide mode of action and sugarbeet injury symptoms
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Basis for Selectivity of Phenmedipham and Desmedipham on Wild ...
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[65]
Organophosphorus and carbamate pesticides
The insecticidal properties of organophosphorus (OP) and carbamate compounds were first discovered in the 1930s, and the compounds were developed for ...
[66]
An Introduction to Insecticides (4th edition)
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[PDF] Special Report 15/2020: Protection of wild pollinators in the EU
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Carbamate pesticides: a general introduction (EHC 64, 1986)
The salts and esters of substituted carbamic acid are more stable than carbamic acid. This enhanced stability is the basis for the synthesis of many derivatives ...<|control11|><|separator|>
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Analytical Evaluation of Carbamate and Organophosphate ...
The LOD and LOQ for all the pesticides of interest ranged from 0.05–0.38 μg/L and 0.15–1.1 μg/L, respectively. These results proved this method to be highly ...
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Pesticides impacts on human health and the environment with their ...
Apr 15, 2024 · This review explored a comprehensive summary of pesticides regarding their updated impacts on human health and advanced safety concerns with legislation.