Insensitive Munitions Research Articles

Dissolution and Transport of Insensitive Munitions Fomulation Imx-104: Overland Flow in Rills

Dissolution and Transport of Insensitive Munitions Fomulation Imx-104: Overland Flow in Rills

Response Surface Methodology for Performance Evaluation of Insensitive Munitions Wastewater Membrane Filtration

Response Surface Methodology for Performance Evaluation of Insensitive Munitions Wastewater Membrane Filtration

Oxidative degradation of nitroguanidine (NQ) by UV-C and oxidants: Hydrogen peroxide, persulfate and peroxymonosulfate

Nitroguanidine (NQ), a component used in insensitive munitions formulations, has high solubility which often leads to highly contaminated wastewater streams. In this work, batch experiments were conducted to investigate and compare the NQ degradation by UV-based advanced oxidation processes (AOPs); hydrogen peroxide (H2O2), persulfate (PS) and peroxymonosulfate (PMS) were selected as oxidants. A preliminary evaluation of AOPs kinetics, byproducts, and potential degradation pathways were carried out and compared to NQ degradation by direct UV-C photolysis. The effects of oxidant dosage, NQ concentrations and pH were evaluated by determining the respective kinetic constants of degradation. Among the treatments applied, UV/PS showed to be a promising and effective alternative leading to faster rates of degradation respect to both oxidant dosage (25 mM) and initial NQ concentrations (≤24 mM). Nevertheless, the degradation rate of NQ by UV/PS appeared to be affected strongly by the initial pH compared to UV/H2O2 and UV/PMS, with the lowest rate overall at pH ≥ 8.0. In addition, the main byproducts from NQ degradation, guanidine and cyanamide, showed to be involved in further degradation steps only with UV/PS and UV/PMS suggesting higher degradation effectiveness of these oxidants compared UV/H2O2 and UV alone.

High-pressure structural stability and melting performance of α-2,4-dinitroanisole

Energetic materials have to face variable environments throughout their life cycle. Therefore, revealing the evolvement of energetic materials under complex conditions is of great importance for their applications. As an energetic material, α-2,4-Dinitroanisole (α-DNAN) exhibits low sensitivity and can be used in the formulation of melt-cast insensitive munitions as a replacement for TNT. Despite numerous studies focusing on DNAN, the high-pressure investigation of DNAN is still limited. Using diamond anvil cell and resistance heating techniques, this study investigates the structural variation and melting performance of α-DNAN at high pressures. The results are as follows. A phase transition occurred at 1.5 ​GPa. The high-pressure phase kept stable and had the tendency to be amorphous at high pressures. The high-temperature and high-pressure Raman measurement and optical photographing illustrated that pressure significantly influenced the melting temperature of α-DNAN. From 0.6 to 1.2 and then to 1.9 ​GPa, the melting point increased from 130 ​°C to 182 ​°C and finally to 285 ​°C. When the pressure reached 1.9 ​GPa, decomposition occurred and was accompanied by a melting process. This high-pressure and high-temperature study of DNAN contributes to deeply understanding the structural stability of DNAN and provides important data for the manufacture and storage of DNAN.

Experimental and simulative thermal stability study of HTPE solid propellants in different scales

The hydroxyl-terminated polyether (HTPE) solid propellants are widely recognized as promising alternatives for hydroxyl-terminated polybutadiene (HTPB) propellants due to their compliance with insensitive munition characteristics of composite solid propellant. This study reports thermal stability investigation of HTPE solid propellants in different scales with the help of differential scanning calorimetry (DSC, 0.9 mg), accelerating rate calorimetry (ARC, 0.219 g), and slow cook-off (112 g) tests by taking HTPE/A3/Al/AP/PSAN composite solid propellant as an example. More importantly, for the first time, thermal decomposition kinetic parameters of HTPE solid propellant were calculated by employing iso-conversional Friedman method and using DSC experimental data at different heating rates. The simulation results of adiabatic combustion and slow cook-off of the HTPE propellant were obtained by applying the kinetic parameters in Advanced Kinetics and Technology Solutions software, which exhibited satisfied consistency with the experimental results, with less than 2% average deviation. Finally, the validated kinetic parameters were further employed to describe the large-scale thermal hazards of HTPE propellant and the predicted self-accelerating decomposition temperature of HTPE propellant in 50 kg-scale was 94.2 °C. Our simulative study provided a cogent and convenient strategy to understand thermal hazard of HTPE solid propellant in different scales during usage, storage, and transportation.

Method for derivatization and isotopic analysis of the insensitive munition compound 3-nitro-1,2,4-triazol-5-one (NTO)

This paper describes an offline low-temperature derivatization method combined with gas chromatography-isotope ratio mass spectrometry (GC-IRMS) to enable compound-specific isotope analysis (CSIA) of C and N in the explosive compound 3-nitro-1,2,4-triazole-5-one (NTO). NTO is being used widely as a component of insensitive munition (IM) composites such as IMX-101, a formulation that is being used to replace the more shock sensitive TNT in artillery shells. The alkylation of NTO with methyl iodide (MeI) as the derivatization reagent was performed in acetone solution at room temperature using triethylamine (Et3N) as a base catalyst. The methylated product of NTO derivatization was identified as 4-methyl-3-nitro-1,2,4-triazol-5-one (MNTO). Accurate and reproducible results were achieved by systematic optimization of MeI and Et3N concentrations and reaction time. Isotopic values of MNTO obtained by GC-IRMS were normalized against those of two 2,4-dinitroanisole (DNAN) in-house reference materials that had been calibrated with isotopic standard reference materials, USGS40 and USGS41a. The resulting method detection limit for derivatization/GC-IRMS of NTO was 788ng of NTO, yielding a precision of ±0.3‰ for both δ13C and δ15N values in good agreement with δ13C and δ15N values for NTO determined by elemental analyzer-IRMS.

Removal of munition constituents in stormwater runoff: Screening of native and cationized cellulosic sorbents for removal of insensitive munition constituents NTO, DNAN, and NQ, and legacy munition constituents HMX, RDX, TNT, and perchlorate.

Technologies are needed to address contamination with energetic compounds at military installations. This research developed and evaluated novel and sustainable materials that can be used to remove munition constituents (MC) from stormwater runoff. Initial work focused on 3-nitro-1,2,4-triazol-5-one (NTO), as it is both highly soluble and ionized at environmentally relevant pH values. Screening cellulosic materials indicated that cationized (CAT) versions of pine shavings (pine, henceforth) and burlap (jute) demonstrated >70% removal of NTO from artificial surface runoff. CAT materials also demonstrated >90% removal of the anionic propellant perchlorate. NTO removal (~80%) by CAT pine was similar across initial pH values from 4 to 8.5 S.U. An inverse relationship was observed between NTO removal and the concentration of the major anions chloride, nitrate, and sulfate due to competition for anion binding sites. Sorption isotherms were performed using a mixture of the three primary legacy explosives (octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX), hexahydro-1,3,5-trinitro-s-triazine (RDX), 2,4,6-trinitrotoluene (TNT)), the three insensitive MC (nitroguanidine (NQ), NTO, 2,4-dinitroanisole (DNAN)), and perchlorate. Isotherm results indicated that effective removal of both legacy and insensitive MC would best be achieved using a mixture of peat moss plus one or more of the cationized cellulosic materials.

Reductive Transformation of 3-Nitro-1,2,4-triazol-5-one (NTO) by Leonardite Humic Acid and Anthraquinone-2,6-disulfonate (AQDS).

3-Nitro-1,2,4-triazol-5-one (NTO) is a major and the most water-soluble constituent in the insensitive munition formulations IMX-101 and IMX-104. While NTO is known to undergo redox reactions in soils, its reaction with soil humic acid has not been evaluated. We studied NTO reduction by anthraquinone-2,6-disulfonate (AQDS) and Leonardite humic acid (LHA) reduced with dithionite. Both LHA and AQDS reduced NTO to 3-amino-1,2,4-triazol-5-one (ATO), stoichiometrically at alkaline pH and partially (50-60%) at pH ≤ 6.5. Due to NTO and hydroquinone speciation, the pseudo-first-order rate constants (kObs) varied by 3 orders of magnitude from pH 1.5 to 12.5 but remained constant from pH 4 to 10. This distinct pH dependency of kObs suggests that NTO reactivity decreases upon deprotonation and offsets the increasing AQDS reactivity with pH. The reduction of NTO by LHA deviated continuously from first-order behavior for >600 h. The extent of reduction increased with pH and LHA electron content, likely due to greater reactivity of and/or accessibility to hydroquinone groups. Only a fraction of the electrons stored in LHA was utilized for NTO reduction. Electron balance analysis and LHA redox potential profile suggest that the physical conformation of LHA kinetically limited NTO access to hydroquinone groups. This study demonstrates the importance of carbonaceous materials in controlling the environmental fate of NTO.

Iron(II) monosulfide (FeS) minerals reductively transform the insensitive munitions compounds 2,4-dinitroanisole (DNAN) and 3-nitro-1,2,4-triazol-5-one (NTO)

As military applications of the insensitive munitions compounds (IMCs) 2,4-dinitroanisole (DNAN) and 3-nitro-1,2,4-triazol-5-one (NTO) increase, there is a growing need to understand their environmental fate and to develop remediation strategies to mitigate their impacts. Iron (II) monosulfide (FeS) minerals are abundant in freshwater and marine sediments, marshes, and hydrothermal environments. This study shows that FeS solids can reduce DNAN and NTO to their corresponding amines under anoxic ambient conditions. The reactions between IMCs and the FeS minerals were surface-mediated since they did not occur when only dissolved Fe2+(aq) and S2−(aq) were present. Mackinawite, a tetragonal FeS with a layered structure, reduced DNAN mainly to 2-methoxy-5-nitroaniline (MENA), which in turn was partially reduced to 2-4-diaminoanisole (DAAN). The layered structure of mackinawite provided intercalation sites likely responsible for partial adsorption of MENA and DAAN. Mackinawite entirely reduced NTO to 3-amino-1,2,4-triazol-5-one (ATO). The reduction of IMCs showed concurrent oxidation of mackinawite to goethite and elemental sulfur. A commercial FeS product, composed mainly of pyrrhotite and troilite, reduced DNAN to DAAN and NTO to ATO. At pH 6.5, DNAN and NTO transformation rates were 667 and 912 μmol h−1 m−2, respectively, on the mackinawite surface and 417 and 1344 μmol h−1 m−2, respectively, on the commercial FeS surface. This is the first report of the reduction of a nitro-heterocyclic compound (NTO) by FeS minerals. The evidence indicates that DNAN and NTO can be rapidly transformed to their succeeding amines in anoxic subsurface environments and aquatic sediments rich in FeS minerals.

Mode of action evaluation for reduced reproduction in Daphnia pulex exposed to the insensitive munition, 1-methyl-3-nitro-1-nitroguanidine (MeNQ)

The US Department of Defense (DOD) is developing insensitive munitions (IMs) that are resistant to unintended detonation to protect warfighters. To enable material life-cycle analysis for the IM, 1-methyl-3-nitro-1-nitroguanidine (MeNQ), ecotoxicological impacts assessment was required. A previous investigation of MeNQ exposures in Daphnia pulex revealed concentration-responsive decreases in reproduction relative to controls (0 mg/L) across a 174, 346, 709, 1385, and 2286 mg/L exposure range. The present study used those exposures to conduct global transcriptomic expression analyses to establish hypothetical mode(s) of action underlying inhibited reproduction. The number of significantly affected transcripts and the magnitude of fold-change differences relative to controls tended to increase with increasing MeNQ concentration where hierarchical clustering analysis identified separation among the “low” (174 and 346 mg/L) and “high” (709, 1385, and 2286 mg/L) exposures. Vitellogenin is critical to Daphnia reproductive processes and MeNQ exposures significantly decreased transcriptional expression for vitellogenin-1 precursor at the lowest exposure level (174 mg/L) with benchmark dose (BMD) levels closely tracking concentrations that caused inhibited reproduction. Additionally, juvenile hormone-inducible protein, chorion peroxidase, and high choriolytic enzyme transcriptional expression were impacted by MeNQ exposure having potential implications for egg production / maturation and overall fecundity. In concert with these effects on specific genes involved in Daphnia reproductive physiology, MeNQ exposures caused significant enrichment of several canonical-pathways responsible for metabolism of cellular energy substrates where BMD levels for transcriptional expression were observed at ≤100 mg/L. These observations imply possible effects on whole-organism energy budgets that may also incur indirect costs on reproduction.

Physicochemical Parameters of Insensitive Munition Constituent Methylnitroguanidine (MeNQ) of Importance to Environmental Fate and Transport

Abstract1‐methyl‐3‐nitroguandine (MeNQ) is being pursued as an insensitive munition to replace legacy munitions such as TNT and RDX. This study was intended to determine the basic physicochemical properties of MeNQ as well as potential environmental fate pathways. The solubility of MeNQ was determined to be 12.92±0.52 g/L and aqueous photolysis was found to efficiently degrade the munition, where its quantum yield and half‐life were found to be 0.009 and 0.59 days, respectively. Hydrolysis was an insignificant degradation pathway resulting in 8.1 % degradation at pH 4, 2.6 % at pH 7, and 6.2 % at pH 9 after five days at an elevated temperature. Volatilization at environmentally relevant conditions was found to be insignificant as the molecule thermally degrades, leading to an inability to calculate Henry's Constant for volatilization from water. Spectroscopic (UV‐vis, FTIR, NMR) and analytical (HPLC) studies were undertaken and are shown alongside the parent molecule, NQ, for comparison to characterize the emerging munition.

Accumulation of Insensitive Munition Compounds in the Earthworm Eisenia andrei from Amended Soil: Methodological Considerations for Determination of Bioaccumulation Factors.

The present study investigates the bioaccumulation of the insensitive munition compounds 2,4-dinitroanisole (DNAN) and 3-nitro-1,2,4-triazol-5-one (NTO), developed for future weapons systems to replace current munitions containing sensitive explosives. The earthworm Eisenia andrei was exposed to sublethal concentrations of DNAN or NTO amended in Sassafras sandy loam. Chemical analysis indicated that 2- and 4-amino-nitroanisole (2-ANAN and 4-ANAN, respectively) were formed in DNAN-amended soils. The SumDNAN (sum of DNAN, 2-ANAN, and 4-ANAN concentrations) in soil decreased by 40% during the 14-d exposure period. The SumDNAN in the earthworm body residue increased until day 3 and decreased thereafter. Between days 3 and 14, there was a 73% decrease in tissue uptake that was greater than the 23% decrease in the soil concentration, suggesting that the bioavailable fraction may have decreased over time. By day 14, the DNAN concentration accounted for only 45% of the SumDNAN soil concentration, indicating substantial DNAN transformation in the presence of earthworms. The highest bioaccumulation factor (BAF; the tissue-to-soil concentration ratio) was 6.2 ± 1.0 kg/kg (dry wt) on day 3 and decreased to 3.8 ± 0.8 kg/kg by day 14. Kinetic studies indicated a BAF of 2.3 kg/kg, based on the earthworm DNAN uptake rate of 2.0 ± 0.24 kg/kg/d, compared with the SumDNAN elimination rate of 0.87 d-1 (half-life = 0.79 d). The compound DNAN has a similar potential to bioaccumulate from soil compared with trinitrotoluene. The NTO concentration in amended soil decreased by 57% from the initial concentration (837 mg NTO/kg dry soil) during 14 d, likely due to the formation of unknown transformation products. The bioaccumulation of NTO was negligible (BAF ≤ 0.018 kg/kg dry wt). Environ Toxicol Chem 2021;40:1713-1725. © 2021 SETAC. This article has been contributed to by US Government employees and their work is in the public domain in the USA.

Outdoor dissolution and photodegradation of insensitive munitions formulations IMX-101 and IMX-104: Photolytic transformation pathway and mechanism study

New munition compounds have been developed to replace traditional explosives to prevent unintended detonations. However, insensitive munitions (IM) can leave large proportion of unexploded charge in the field, where it is subjected to photodegradation and dissolution in precipitation. The photolytic reactions occurring on the surfaces of IMX-101 and IMX-104 formulations and the subsequent fate of photolytic products in the environment were thoroughly investigated. The constituents of IMX-101 and IMX-104 formulations dissolve sequentially under rainfall in the order of aqueous solubility: 3-nitro-1,2,4-triazol-5-one (NTO) > nitroguanidine (NQ) > 2,4-dinitroanisole (DNAN) > 1,3,5-hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). A linear relationship between DNAN dissolution and rainwater volume was observed (r2: 0.86–0.99). It was estimated that it would take 16–228 years to completely dissolve these formulation particles under natural environmental conditions in Oracle, AZ. We used LC/MS/MS and GC/MS to examine the dissolution samples from IMX-101 and 104 particles exposed to rainfall and sunlight and found six DNAN photo-transformation products including 2-methoxy-5-nitrophenol, 4-methoxy-3-nitrophenol, 4-methoxy-3-nitroaniline, 2-methoxy-5-nitroaniline, 2,4-dinitrophenol, and methoxy-dinitrophenol, which are in good agreement with computational modeling results of bond strengths. The main DNAN photodegradation pathways are therefore proposed. Predicted eco-toxicity values suggested that the parent compound DNAN, methoxy-nitrophenols, methoxy-nitroanilines and the other two products (2,4-dinitrophenol and methoxy-dinitrophenol) would be harmful to fish and daphnid. Our study provides improved insight about the rain dissolution and photochemical behavior of IM formulations under natural conditions, which helps to form target-oriented strategies to mitigate explosive contamination in military training sites.

Selecting the best electron donor and operational temperature for the rapid biotransformation of the insensitive munitions compound 2,4-dinitroanisole (DNAN) by anaerobic sludge.

2,4-Dinitroanisole (DNAN) is a toxic compound increasingly used by the military that can be released into the environment on the soil of training fields and in the wastewater of manufacturing plants. DNAN's nitro groups are anaerobically reduced to amino groups by microorganisms when electron donors are available. Using anaerobic sludge as the inoculum, we tested different electron donors for DNAN bioreduction at 20 and 30 °C: acetate, ethanol, pyruvate, hydrogen, and hydrogen + pyruvate. Biotic controls without external electron donors and abiotic controls with heat-killed sludge were also assayed. No DNAN conversion was observed in the abiotic controls. In all biotic treatments, DNAN was reduced to 2-methoxy-5-nitroaniline (MENA), which was further reduced to 2,4-diaminoanisole (DAAN). Ethanol or acetate did not increase DNAN reduction rate compared to the endogenous control. The electron donors that caused the fastest DNAN reductions were (rates at 30 °C): H2 and pyruvate combined (311.28 ± 10.02 μM·d-1·gSSV-1), followed by H2 only (207.19 ± 5.95 μM·d-1·gSSV-1), and pyruvate only (36.35 ± 2.95 μM·d-1·gSSV-1). Raising the temperature to 30 °C improved DNAN reduction rates when pyruvate, H2, or H2 + pyruvate were used as electrons donors. Our results can be applied to optimize the anaerobic treatment of DNAN-containing wastewater.

The investigation of NTO/HMX-based plastic-bonded explosives and its safety performance

3-nitro-1,2,4-triazol-5-one (NTO) is the main component of insensitive munitions (IM) formulation because of its outstanding insensitive properties. In this paper, a series of NTO/HMX-based composite explosives were prepared and characterized. The study focuses on the effect of NTO on the performance of the formulations, especially the safety performance. The results revealed that the mechanical sensitivity of formulations was associated with NTO content, as well as the thermal conductivity, specific heat capacity and Arrhenius parameters. Then, the high amount of NTO using in formulation was proved to be helpful for NTO/HMX-based formulation to exhibit good thermal safety. Besides, by accelerating rate calorimeter (ARC) and a modified cook-off equipment, the pressure and pressure rise rate were proved as the important indicator for judging the thermal safety performance in confined spaces. Finally, the numerical simulation was used as a credible method for predicting the respond temperature of cook-off experiment.

Oxidant‐Accelerated Polydopamine Modification Process for the Fast Fabrication of PDA on HMX with Improved Mechanical Stability

AbstractPolydopamine surface coating shows the capability to improve the adhesive properties as well as mechanical stabilities of energetic materials, which is highly desired for the development of insensitive munitions. However, the slow polymerization process of dopamine makes the coating process time‐consuming and uneconomic. Herein, an oxidant‐accelerated strategy was demonstrated to obtain fast polymerization kinetics of dopamine for the surface modification of HMX crystals. Upon the addition of oxidant, PDA was able to form surface layer of HMX particles within 5 min without changing the shape and polymorph of HMX crystals. The PDA coating showed the ability to improve the wettability of HMX, contributing to its abundant active groups. Moreover, the mechanical stability of PDA on HMX (HMX@PDA) samples was improved accompany with the increasing coating time, and the friction explosion probability and drop height of 300 s treated sample were 40 % and 64 cm, respectively. The detonation velocity was also measured, which showed that the effect of PDA coating on the detonation velocity of HMX was not significant. More importantly, our protocol showed the capability to fabricate HMX@PDA with different particle sizes on a large scale, satisfying the application demands of insensitive high explosives.

Covalent binding with model quinone compounds unveils the environmental fate of the insensitive munitions reduced product 2,4-diaminoanisole (DAAN) under anoxic conditions

2,4-Dinitroanisole (DNAN) is an insensitive munitions compound expected to replace 2,4,6-trinitrotoluene (TNT). The product of DNAN’s reduction in the environment is 2,4-diaminoanisole (DAAN), a toxic and carcinogenic aromatic amine. DAAN is known to become irreversibly incorporated into soil natural organic matter (NOM) after DNAN’s reduction. Herein, we investigate the reactions between DAAN and NOM under anoxic conditions, using 1,4-benzoquinone (BQ) and methoxybenzoquinone (MBQ) as model humic moieties of NOM. A new method stopped the fast reactions between DAAN and quinones, capturing the fleeting intermediates. We observed that DAAN incorporation into NOM (represented by BQ and MBQ models) is quinone-dependent and occurs via Michael addition, imine (Schiff-base) formation, and azo bond formation. After dimers are formed, incorporation reactions continue, resulting in trimers and tetramers. After 20 days, 56.4% of dissolved organic carbon from a mixture of DAAN (1 mM) and MBQ (3 mM) had precipitated, indicating an extensive polymerization, with DAAN becoming incorporated into high-molecular-weight humic-like compounds. The present work suggests a new approach for DNAN environmental remediation, in which DNAN anaerobic transformation can be coupled to the formation of non-extractable bound DAAN residues in soil organic matter. This process does not require aerobic conditions nor a specific catalyst.

Insensitive High Explosives: V. Ballistic Properties and Vulnerability of Nitroguanidine Based Propellants

AbstractThis paper reviews the ballistic properties, stability and vulnerability of gun propellants, gas generators and rocket propellants containing nitroguanidine (NGu), CAS−No [556‐88‐7] as an energetic filler. Nitroguanidine and its formulations burn stable over a broad pressure regime extending from subatmospheric to high pressures (0.1 kPa–400 MPa). Its high nitrogen content (53.83 %) and oxygen balance (Ω=‐30.75 %) effects a high gas pressure in gun propellants combined with low explosion temperature and consequently low signature and reduced erosion. NGu is an effective stabilizer for a broad array of energetic materials encountered in gun and rocket propellants including AP, ADN, HMX, RDX, NGl and also materials with low thermal stability such as NC, HNF, TNAZ and ADN. Finally, the low vulnerability of NGu‐based propellant formulations makes them taylor made to serve insensitive munitions. This review covers 31 NGu‐based rocket and gas generating propellant formulations, 44 gun propellants, five of which contain guanylurea dinitramide, (GuDN, FOX‐12), CAS−No [217464‐38‐5] for comparison, four reference propellants containing neither of the aforementioned ingredients and six combustible cartridge case formulations based on NGu. In addition, the combustion properties of pure NGu, pure GUDN and NGu modified with 17 different catalysts are revised. The review contains 142 references from the public domain.

Catalytic role of solvated electron in the spontaneous degradation of insensitive munition compounds: computational chemistry investigation

The DNAN (2,4-dinitroanisole), NTO (3-nitro-1,2,4-triazol-5-one), and NQ (nitroguanidine) are important insensitive energetic materials used in military applications. They may find their way to the environment during manufacturing, transportation, storage, training, and disposal. A detailed investigation of possible mechanisms for self-degradation of radical anions formed by addition of solvated electron to DNAN, NTO, and NQ species was performed by computational study using the PCM(Pauling)/M06-2X/6-311++G(d,p) approach. Obtained results suggest that only NQ radical anion is able for self-degradation by elimination of nitrite anion. Formation of urea radical on the earlier stage of the NQ radical anion degradation was also predicted.

Multi-species Aquatic Toxicity Assessment of 1-Methyl-3-Nitroguanidine (MeNQ).

The Army is replacing traditional munitions with insensitive munitions (IM) resistant to accidental detonation. The aquatic toxicity of 1-methyl-3-nitroguanidine (MeNQ), which is being assessed for potential use in IM formulations, remains largely untested. The present study fills a number of critical data gaps for MeNQ aquatic toxicity by evaluating effects across two vertebrate and five invertebrate species. Specifically, responses in larval Pimephales promelas, Rana pipiens tadpoles, Chironomus dilutus, Lumbriculus variegatus, Hydra littoralis, Hyalella azteca, and Daphnia pulex were assessed in MeNQ exposures across various acute, subchronic, and chronic bioassays. Overall, survival was unaffected in most of the MeNQ exposures where significant lethal effects were only observed in D. pulex, H. littoralis, and C. dilutus and only at concentrations ≥ 2186mg/L. Significant sublethal effects on growth were observed for C. dilutus at 903mg/L and H. azteca at 1098mg/L in 10-d assays. Significantly decreased reproduction was observed at 2775mg/L for H. azteca in a chronic 35-d assay and at 174mg/L for D. pulex in the 11-d three-brood assay representing a sublethal effect one order of magnitude more sensitive than the effective lethal concentration for D. pulex (2987mg/L). Degradation of MeNQ in ultraviolet light (UV) greatly increased toxicity to D. pulex. Specifically, exposure to a MeNQ solution that was completely UV-degraded prior to D. pulex exposures resulted in an 11-d LC50 of 6.1mg/L and a 50% reduction in reproduction at 3.125mg/L, based on the original MeNQ parent-compound concentrations.