Structure of 122628-50-6
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Methoxatin Disodium is used as a cofactor (prosthetic group) for enzyme-catalyzed redox reactions of glucose and methanol dehydrogenases.
Synonyms: PQQ disodium salt; Methoxatin disodium salt
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| CAS No. : | 122628-50-6 |
| Formula : | C14H4N2Na2O8 |
| M.W : | 374.17 |
| SMILES Code : | O=C(C1=NC2=C(C(NC(C(O)=O)=C3)=C3C(C2=O)=O)C(C([O-])=O)=C1)[O-].[Na+].[Na+] |
| Synonyms : |
PQQ disodium salt; Methoxatin disodium salt
|
| MDL No. : | MFCD00151711 |
| InChI Key : | UFVBOGYDCJNLPM-UHFFFAOYSA-L |
| Pubchem ID : | 3078772 |
| GHS Pictogram: |
|
| Signal Word: | Warning |
| Hazard Statements: | H302 |
| Precautionary Statements: | P264-P270-P301+P312-P330-P501 |
In Vitro:
|
Cell Line
|
Concentration | Treated Time | Description | References |
| HEI-OC1 auditory cells | 0.1 nM or 1.0 nM | 1 day | To investigate the protective effects of PQQ on the H2O2-induced premature senescence model in HEI-OC1 auditory cells and elucidate its mechanism of action. Results showed that PQQ pretreatment restored mitochondrial respiratory capacity, reduced mitochondrial potential decline, promoted mitochondrial fusion, and accelerated mitochondrial movement. Additionally, PQQ pretreatment significantly increased the protein expression of SIRT1 and PGC-1α and decreased PGC-1α acetylation. | NPJ Aging. 2022 Apr 19;8(1):3 |
| SH-SY5Y cells | 5 µM | 12 hours | To evaluate the protective effect of PQQ against Aβ1-42-induced neurotoxicity. Results showed PQQ effectively reduced ROS production. | Adv Sci (Weinh). 2024 May;11(18):e2308970 |
| L6 myotubes | 0.5 µM | 2 hours | To evaluate the effect of PQQ on lipid metabolism in insulin-resistant L6 myotubes, showing that short-term PQQ treatment decreased free fatty acids and triacylglycerols levels. | Int J Mol Sci. 2020 Nov 8;21(21):8382 |
| Retinal cells | 50 µM | 2 hours | To assess the effect of PQQ on ATP content, results showed an increase in ATP levels | Acta Neuropathol Commun. 2023 Sep 8;11(1):146 |
| Mouse brain cortical cells | 0.1, 0.5, 1, 5, 10, 50 µM | 2 hours | To assess the effect of PQQ on ATP content, results showed a significant increase in ATP levels | Acta Neuropathol Commun. 2023 Sep 8;11(1):146 |
| Kupffer cells | 10, 50 and 100 nM | 2 hours | Simulated sepsis-induced acute liver injury, PQQ treatment alleviated inflammation, oxidative stress and apoptosis in LPS-induced Kupffer cells | Bioengineered. 2021 Dec;12(1):2459-2468 |
| BV2 microglia cells | 0.1, 1, 10 µM | 2 hours pretreatment followed by 12 hours incubation | PQQ pretreatment significantly decreased rotenone-induced lactate dehydrogenase (LDH) release and suppressed the up-regulation of pro-inflammatory factors (IL-1β, IL-6, TNF-α) and NO release. Additionally, PQQ pretreatment increased the ratio of LC3-II/LC3-I and expression of Atg5, indicating enhanced autophagy. | Molecules. 2020 Sep 23;25(19):4359 |
| L6 myotubes | 0.5 µM | 24 hours | To evaluate the effect of PQQ on lipid metabolism in insulin-resistant L6 myotubes, showing that long-term PQQ treatment increased diacylglycerols and triacylglycerols levels. | Int J Mol Sci. 2020 Nov 8;21(21):8382 |
| SH-SY5Y cells | 0.1, 1, 10 µM | 24 hours | The conditioned medium (CM) from PQQ-pretreated BV2 cells significantly increased the viability of SH-SY5Y cells, indicating that PQQ protects neuronal cells from damage by inhibiting microglia-mediated inflammatory responses. | Molecules. 2020 Sep 23;25(19):4359 |
| TM3 cells | 100 nM | 24 hours | To investigate the effect of PQQ on testosterone synthesis and cholesterol metabolism in PA-treated TM3 cells. Results showed that PQQ significantly increased intracellular cholesterol levels and testosterone synthesis, while reducing LDH release and PI uptake. | Cell Death Dis. 2023 Nov 7;14(11):723 |
| KGN cells | 20 µM | 24 hours | To evaluate the effects of PQQ and MSC-Mito on mitochondrial function and oxidative stress in KGN cells. The results showed that the combined treatment significantly restored mitochondrial membrane potential and ATP production, reduced ROS and MDA levels, and increased SOD content. | Stem Cell Res Ther. 2024 Apr 5;15(1):97 |
| Primary chicken hepatocytes | 50, 100, 200 nM | 24 hours | Improves lipid metabolism and hepatocyte tolerance to fatty degeneration and oxidative damage by enhancing mitochondrial biogenesis, thereby increasing anti-oxidative activity and anti-apoptosis capacity | Int J Mol Sci. 2021 Feb 1;22(3):1458 |
| Human BM-MSCs | 1, 5, 10, 20 µM | 24 hours | To detect the effect of PQQ on the expression of Nrf2 and Keap1 | Aging Cell. 2023 Sep;22(9):e13912 |
| Primary cardiomyocytes | 100 µM | 24 hours | Evaluate the effect of PQQ on PE-induced cardiomyocyte hypertrophy, results showed PQQ significantly alleviated PE-induced hypertrophic activity | Front Pharmacol. 2022 Sep 27;13:977385 |
| H9C2 cardiomyocytes | 1-200 µM | 24 hours | Evaluate the effect of PQQ on cell viability, results showed no cytotoxicity at 1-200 μM PQQ concentrations | Front Pharmacol. 2022 Sep 27;13:977385 |
| HL-1 cardiomyocytes | 1-200 µM | 24 hours | Evaluate the effect of PQQ on cell viability, results showed no cytotoxicity at 1-200 μM PQQ concentrations | Front Pharmacol. 2022 Sep 27;13:977385 |
| MLE-12 alveolar type II epithelial cells | 40 µM | 24 hours | To assess the effect of PQQ on PM2.5-induced cell migration capacity. Results showed that PQQ significantly attenuated the enhanced migratory ability induced by PM2.5. | J Cell Mol Med. 2024 Apr;28(8):e18299 |
| MLE-12 alveolar type II epithelial cells | 40 µM | 24 hours | To investigate the inhibitory effect of PQQ on PM2.5-induced epithelial-mesenchymal transition (EMT). Results showed that PQQ reversed PM2.5-induced changes in cell morphology and reduced the expression of mesenchymal markers Vimentin and Snail. | J Cell Mol Med. 2024 Apr;28(8):e18299 |
| MLE-12 alveolar type II epithelial cells | 10, 20, 40 µM | 24 hours | To evaluate the inhibitory effect of PQQ on PM2.5-induced upregulation of collagen expression. Results showed that PQQ significantly reduced COL1A1 protein expression in a dose- and time-dependent manner. | J Cell Mol Med. 2024 Apr;28(8):e18299 |
| AC16 human myocardial cells | 1 and 10 nM | 24 hours | To investigate the protective effects of PQQ on AC16 cells under high glucose conditions. Results showed that 10 nmol/L PQQ significantly reduced high glucose-induced cell damage, inhibited NLRP3 inflammasome activation and NF-κB signaling pathway, decreased ROS production, and improved mitochondrial membrane potential. | Eur J Nutr. 2022 Jun;61(4):1823-1836 |
| 16-HBE cells | 5-80 µM | 24 or 48 hours | To examine the cytotoxicity of PQQ, results showed that PQQ reduced 16-HBE cell viability in a dose-dependent manner, but cell viability remained above 70% at 5-80 μM. | Mediators Inflamm. 2022 Oct 29;2022:1267841 |
| H9c2 cells | 1, 2.5, 5 µM | 3 hours pretreatment followed by 24 hours exposure to Iso | To investigate the protective effects of PQQ against Iso-induced cardiac hypertrophy. Results showed that PQQ pretreatment significantly reduced Iso-induced cardiac hypertrophy, consistent with the results in AC16 cells. | Int J Mol Med. 2020 Mar;45(3):873-885 |
| AC16 cells | 1, 2.5, 5 µM | 3 hours pretreatment followed by 24 hours exposure to Iso | To investigate the protective effects of PQQ against Iso-induced cardiac hypertrophy. Results showed that PQQ pretreatment significantly inhibited the expression of cardiac hypertrophy marker proteins, such as atrial natriuretic peptide, brain natriuretic peptide and β-myosin heavy chain, and inhibited the activation of the NF-κB signaling pathway. | Int J Mol Med. 2020 Mar;45(3):873-885 |
| SH-SY5Y cells | 100 µM | 30 minutes | To investigate the protective effects of PQQ on rotenone-injured SH-SY5Y cells and its mechanisms. Results showed that PQQ promoted mitochondrial biogenesis via activation of the AMPK signaling pathway and alleviated rotenone-induced cell injury. | Acta Pharmacol Sin. 2021 May;42(5):665-678 |
| Mouse brain microvascular endothelial bEND.3 cells | 1, 10, 100 µM | 48 or 72 hours | To investigate the protective effect of PQQ on high glucose-induced damage in bEND.3 cells. Results showed that PQQ significantly reversed high glucose-induced cell viability reduction, suppressed apoptosis and ROS production, and restored mitochondrial membrane potential and number. | Acta Pharmacol Sin. 2014 Nov;35(11):1402-10 |
| CD4+ T cells | 20-80 µM | 5 days | To test the effect of PQQ on Th2 cell differentiation, results showed that PQQ significantly inhibited IL-4 and IL-5 production in a dose-dependent manner. | Mediators Inflamm. 2022 Oct 29;2022:1267841 |
| IPEC-J2 cells | 10 nM | 6-hours pretreatment followed by 2-hours co-culture | To evaluate the protective effect of PQQ against H2O2-induced oxidative damage. Results showed that PQQ pretreatment significantly improved cell viability, increased the expression of tight junction proteins (ZO-1, ZO-2, Occludin, Claudin-1), reduced ROS and MDA levels, and upregulated nuclear Nrf2 and HO-1 protein expression. | J Anim Sci Biotechnol. 2021 Jun 18;12(1):77 |
| Ram sperm | 0 nM, 10 nM, 100 nM, 1000 nM, 10,000 nM | 96 hours | To evaluate the effect of PQQ on chilled ram sperm quality, results showed that PQQ significantly improved sperm motility, membrane integrity, and acrosome integrity. | Antioxidants (Basel). 2024 Jan 15;13(1):104 |
| Boar sperm | 1000 nM | After freezing-thoursawing | Improved post-thaw sperm motility, viability, and acrosome integrity, reduced oxidative stress, and protected mitochondrial function. | Antioxidants (Basel). 2025 Jan 16;14(1):102 |
In Vivo:
|
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
| Laying hens | High-energy low-protein diet-induced metabolic dysfunction-associated fatty liver disease model | Dietary supplementation | 0.08 and 0.16 mg/kg diet | Continued for 4 weeks | Significantly ameliorated liver biological functions, suppressed the progression of MAFLD mainly through enhanced lipid metabolism and protection of liver from oxidative injury | Int J Mol Sci. 2021 Feb 1;22(3):1458 |
| Duroc × Landrace × Yorkshire crossbred pigs | Weaned piglet model | Oral (dietary supplementation) | 0.15%, 0.30%, 0.45% PQQ·Na2 | 28 days | To investigate the effects of PQQ on growth performance, diarrhea incidence, and redox status in weaned pigs. Results showed that 0.45% PQQ significantly improved average daily gain (ADG) and gain-to-feed ratio (G:F), reduced diarrhea incidence and MDA content in liver and jejunum, and increased SOD activity in liver. 0.3% PQQ decreased ileal and liver MDA concentration, and 0.15% PQQ decreased ileal MDA concentration. | J Anim Sci Biotechnol. 2021 Jun 18;12(1):77 |
| Laying hens | Laying hens performance model | Dietary supplementation | 0.4 mg/kg | 8 weeks | Increased the antioxidant ability of layers and eggs which might be in connection with the activation of the Nrf2/HO-1 pathway and optimized gut microflora | Food Chem X. 2023 Nov 30;20:101021 |
| ICR mice | Rotenone-induced Parkinson’s disease model | Intraperitoneal injection | 0.8, 4, 20 mg/kg/day | Once daily for 3 weeks | To investigate the neuroprotective effects of PQQ in a rotenone-induced Parkinson’s disease mouse model. Results showed that PQQ dose-dependently alleviated locomotor deficits and nigral dopaminergic neuron loss, and promoted mitochondrial biogenesis. | Acta Pharmacol Sin. 2021 May;42(5):665-678 |
| SD rats | Sepsis model | Intraperitoneal injection | 10 mg/kg | Administered 1 hour before surgery and continuously for 2 weeks post-surgery | PQQ treatment alleviated acute liver injury, inflammatory and oxidative stress damage and apoptosis of liver tissue cells in sepsis rats | Bioengineered. 2021 Dec;12(1):2459-2468 |
| Balb/c mice | OVA-induced allergic airway inflammation model | Intraperitoneal injection | 10 mg/kg or 20 mg/kg | Once daily for 11 days | To examine the effect of PQQ on allergic airway inflammation, results showed that PQQ significantly attenuated airway inflammation, reduced BALF inflammatory cell counts, altered the percentages of Th1, Th2, Th17, and Treg cells, and regulated the JAK-STAT signaling pathway. | Mediators Inflamm. 2022 Oct 29;2022:1267841 |
| C57BL/6J mice | High-fat diet-induced obese mouse model | Intragastric administration | 10 mg/kg/day | Once daily for 8 weeks | To investigate the effect of PQQ on lipid metabolism and testosterone synthesis in obese mice. Results showed that PQQ significantly improved abnormal lipid metabolism, increased testosterone levels, and improved testicular structure and sperm quality. | Cell Death Dis. 2023 Nov 7;14(11):723 |
| C57BL/6 mice | Diabetic cardiomyopathy model | Oral | 10, 20, or 40 mg/kg/day | Daily administration for 12 weeks | To investigate the protective effects of PQQ on diabetic cardiomyopathy. Results showed that PQQ significantly alleviated myocardial hypertrophy and fibrosis, enhanced antioxidant function, reduced inflammatory cytokine levels, and inhibited the NF-κB/NLRP3 inflammasome-mediated pyroptosis signaling pathway. | Eur J Nutr. 2022 Jun;61(4):1823-1836 |
| C57BL/6J mice | Chemotherapy-induced premature ovarian insufficiency model | Oral | 15 mg/kg PQQ | Once daily for three weeks | To evaluate the therapeutic effects of PQQ and MSC-Mito on ovarian function in POI mice. The results showed that the combined treatment significantly restored body weight, ovarian volume and relative weight, improved the estrous cycle, increased the number of follicles at various stages, reduced atretic follicles, and restored sex hormone secretion and antioxidant capacity. | Stem Cell Res Ther. 2024 Apr 5;15(1):97 |
| Mice | Retinal axotomy explant model and Rotenone-induced retinal degeneration model | Intraperitoneal injection | 20 mg/kg | Single injection or every 48 hours for 2 weeks | To evaluate the neuroprotective effect of PQQ on retinal ganglion cells, results showed PQQ was neuroprotective in both models | Acta Neuropathol Commun. 2023 Sep 8;11(1):146 |
| C57/BL6 mice | Aβ1-42-induced Alzheimer's disease mouse model | Intragastric administration | 20 mg/kg | Once daily for 14 days | To evaluate the effect of PQQ on cognitive dysfunction. Results showed PQQ significantly improved short-term memory and spatial learning in AD mice. | Adv Sci (Weinh). 2024 May;11(18):e2308970 |
| Sprague-Dawley rats | Oral toxicokinetic study | Oral | 250 mg/kg, 500 mg/kg, 1000 mg/kg | Single dose and 28-day repeated administration | Study the toxicokinetic properties and safety evaluation of PQQ disodium salt | Molecules. 2022 Nov 17;27(22):7947 |
| Duroc × Landrace × Yorkshire crossbred piglets | Enterotoxigenic Escherichia coli K88 infection model | Dietary supplementation | 3 mg/kg | 14 days | To evaluate the effect of PQQ on gut inflammation and microbiota dysbiosis induced by ETEC K88. Results showed that PQQ supplementation significantly alleviated ETEC K88-induced jejunal mucosal barrier function damage and regulated colonic microbiota. | Front Microbiol. 2020 Jul 24;11:1754 |
| Weaned piglets | LPS-induced intestinal inflammation model | Oral | 3.0 mg/kg | 14 days | Alleviated intestinal inflammation and cell apoptosis, improved intestinal barrier function via the MKK3/6-P38 pathway | Int J Mol Sci. 2024 Sep 8;25(17):9723 |
| Pigs | Weaned piglets | Dietary supplementation | 3.0 mg/kg | 28 days | To compare the effects of pyrroloquinoline quinone (PQQ) and zinc oxide (ZnO) on growth performance, diarrhea indices, nutrient digestibility, antioxidant capacity, neurotransmitter levels, and metabolism in weaned pigs. Results showed that both PQQ and ZnO improved growth performance, nutrient digestibility, antioxidant capacity, and regulated neurotransmitter levels in weaned pigs. | Anim Nutr. 2023 Oct 4;15:409-419 |
| C57BL/6 mice | Ovariectomy (OVX)-induced osteoporosis model | Dietary supplementation | 4 mg/kg | Daily for 8 weeks | To evaluate the protective effect of PQQ on ovariectomy-induced osteoporosis. Results showed that PQQ supplementation could prevent OVX-induced bone loss and improve bone strength by inhibiting oxidative stress and osteocyte senescence. | Int J Biol Sci. 2019 Jan 1;15(1):58-68 |
| Mice | Natural aging-induced osteoporosis model | Dietary supplementation | 4 mg/kg diet | Starting from 6 or 12 months of age, lasting for 12 or 6 months | To evaluate the preventive effect of PQQ supplementation on natural aging-induced osteoporosis | Aging Cell. 2023 Sep;22(9):e13912 |
| C57BL/6 male mice | Iso-induced cardiac hypertrophy model | Intraperitoneal injection | 40 mg/kg | Once every 4 days for approximately 5 weeks | To investigate the protective effects of PQQ against Iso-induced cardiac hypertrophy. Results showed that PQQ pretreatment significantly reduced the increase in myocardial cell surface area induced by Iso and decreased the heart weight/body weight ratio. | Int J Mol Med. 2020 Mar;45(3):873-885 |
| C57BL/6 mice | Transverse aortic constriction (TAC)-induced myocardial hypertrophy model | Gavage | 40 mg/kg | Every other day for 6 weeks | Evaluate the effect of PQQ on TAC-induced myocardial hypertrophy and fibrosis, results showed PQQ significantly suppressed myocardial hypertrophy and fibrosis, and inhibited ferroptotic death of hypertrophic myocardial cells | Front Pharmacol. 2022 Sep 27;13:977385 |
| C57BL/6J mice | PM2.5-induced pulmonary fibrosis model | Intraperitoneal injection | 5 mg/kg | Twice a week for 12 weeks | To evaluate the protective effect of PQQ against PM2.5-induced pulmonary fibrosis. Results showed that PQQ significantly reduced collagen deposition, improved pulmonary function, and decreased the expression of EMT markers COL1A1, Vimentin, Snail, and TGF-β. | J Cell Mol Med. 2024 Apr;28(8):e18299 |
| Bio Calculators | ||||
| Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.67mL 0.53mL 0.27mL |
13.36mL 2.67mL 1.34mL |
26.73mL 5.35mL 2.67mL |
|
| Dissolving Methods |
The prepared working fluid is recommended to be prepared now and used up as soon as possible in a short period of time. The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
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Tags: Pyrroloquinoline quinone disodium | PQQ disodium | Methoxatin disodium | Endogenous Metabolite | redox | co-factor | anionic | methylotropic | bacteriasential | nutrient | immune | function | inhibitor | 122628-50-6 |
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| P402 | Store in a dry place. |
| P403 | Store in a well-ventilated place. |
| P404 | Store in a closed container. |
| P405 | Store locked up. |
| P406 | Store in corrosive resistant/ container with a resistant inner liner. |
| P407 | Maintain air gap between stacks/pallets. |
| P410 | Protect from sunlight. |
| P411 | |
| P412 | Do not expose to temperatures exceeding 50 oC/ 122 oF. |
| P413 | |
| P420 | Store away from other materials. |
| P422 | |
| P402 + P404 | Store in a dry place. Store in a closed container. |
| P403 + P233 | Store in a well-ventilated place. Keep container tightly closed. |
| P403 + P235 | Store in a well-ventilated place. Keep cool. |
| P410 + P403 | Protect from sunlight. Store in a well-ventilated place. |
| P410 + P412 | Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. |
| P411 + P235 | Keep cool. |
Disposal | |
| Code | Phrase |
| P501 | Dispose of contents/container to ... |
| P502 | Refer to manufacturer/supplier for information on recovery/recycling |
Physical hazards | |
| Code | Phrase |
| H200 | Unstable explosive |
| H201 | Explosive; mass explosion hazard |
| H202 | Explosive; severe projection hazard |
| H203 | Explosive; fire, blast or projection hazard |
| H204 | Fire or projection hazard |
| H205 | May mass explode in fire |
| H220 | Extremely flammable gas |
| H221 | Flammable gas |
| H222 | Extremely flammable aerosol |
| H223 | Flammable aerosol |
| H224 | Extremely flammable liquid and vapour |
| H225 | Highly flammable liquid and vapour |
| H226 | Flammable liquid and vapour |
| H227 | Combustible liquid |
| H228 | Flammable solid |
| H229 | Pressurized container: may burst if heated |
| H230 | May react explosively even in the absence of air |
| H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
| H240 | Heating may cause an explosion |
| H241 | Heating may cause a fire or explosion |
| H242 | Heating may cause a fire |
| H250 | Catches fire spontaneously if exposed to air |
| H251 | Self-heating; may catch fire |
| H252 | Self-heating in large quantities; may catch fire |
| H260 | In contact with water releases flammable gases which may ignite spontaneously |
| H261 | In contact with water releases flammable gas |
| H270 | May cause or intensify fire; oxidizer |
| H271 | May cause fire or explosion; strong oxidizer |
| H272 | May intensify fire; oxidizer |
| H280 | Contains gas under pressure; may explode if heated |
| H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
| H290 | May be corrosive to metals |
Health hazards | |
| Code | Phrase |
| H300 | Fatal if swallowed |
| H301 | Toxic if swallowed |
| H302 | Harmful if swallowed |
| H303 | May be harmful if swallowed |
| H304 | May be fatal if swallowed and enters airways |
| H305 | May be harmful if swallowed and enters airways |
| H310 | Fatal in contact with skin |
| H311 | Toxic in contact with skin |
| H312 | Harmful in contact with skin |
| H313 | May be harmful in contact with skin |
| H314 | Causes severe skin burns and eye damage |
| H315 | Causes skin irritation |
| H316 | Causes mild skin irritation |
| H317 | May cause an allergic skin reaction |
| H318 | Causes serious eye damage |
| H319 | Causes serious eye irritation |
| H320 | Causes eye irritation |
| H330 | Fatal if inhaled |
| H331 | Toxic if inhaled |
| H332 | Harmful if inhaled |
| H333 | May be harmful if inhaled |
| H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
| H335 | May cause respiratory irritation |
| H336 | May cause drowsiness or dizziness |
| H340 | May cause genetic defects |
| H341 | Suspected of causing genetic defects |
| H350 | May cause cancer |
| H351 | Suspected of causing cancer |
| H360 | May damage fertility or the unborn child |
| H361 | Suspected of damaging fertility or the unborn child |
| H361d | Suspected of damaging the unborn child |
| H362 | May cause harm to breast-fed children |
| H370 | Causes damage to organs |
| H371 | May cause damage to organs |
| H372 | Causes damage to organs through prolonged or repeated exposure |
| H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
| Code | Phrase |
| H400 | Very toxic to aquatic life |
| H401 | Toxic to aquatic life |
| H402 | Harmful to aquatic life |
| H410 | Very toxic to aquatic life with long-lasting effects |
| H411 | Toxic to aquatic life with long-lasting effects |
| H412 | Harmful to aquatic life with long-lasting effects |
| H413 | May cause long-lasting harmful effects to aquatic life |
| H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
Sorry,this product has been discontinued.
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