52-51-7
52-51-7
Chemical Structure
Bronopol
Synonym(s): BNPD; BNPK
- CAS No.: 52-51-7
- Formula:C3H6BrNO4
- Molecular Weight:199.99
IUPAC Name: 2-bromo-2-nitropropane-1,3-diol
InChIKey: LVDKZNITIUWNER-UHFFFAOYSA-N
SMILES: OCC([N+]([O-])=O)(Br)CO
Biological Activity: Bronopol is an antibacterial agent with low toxicity (to mammals) and high activity (especially against Gram-negative bacteria). Bronopol oxidizes protein thiols, inhibits enzymatic activity, and exhibits antibacterial activity. Bronopol is also a formaldehyde releaser[2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Bronopol | 98.0% | Bronopol is an antibacterial agent with low toxicity (to mammals) and high activity (especially against Gram-negative bacteria). Bronopol oxidizes protein thiols, inhibits enzymatic activity, and exhibits antibacterial activity. Bronopol is also a formaldehyde releaser. | ||||||||||||||||||||
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Bronopol (Standard) | ≥98% | Bronopol (Standard) is the analytical standard of Bronopol. This product is intended for research and analytical applications. Bronopol is an antibacterial agent with low toxicity (to mammals) and high activity (especially against Gram-negative bacteria). Bronopol oxidizes protein thiols, inhibits enzymatic activity, and exhibits antibacterial activity. Bronopol is also a formaldehyde releaser. | ||||||||||||||||||||
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Bronopol-d4 | Bronopol-d4 is deuterium labeled Bronopol. Bronopol is an antibacterial agent with low toxicity (to mammals) and high activity (especially against Gram-negative bacteria). Bronopol oxidizes protein thiols, inhibits enzymatic activity, and exhibits antibacterial activity. Bronopol is also a formaldehyde releaser. | |||||||||||||||||||||
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Bromodichloronitromethane | Bromodichloronitromethane is one of Halonitromethanes, which are a recently identified class of disinfection by-products (DBPs) in drinking water. | |||||||||||||||||||||
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Dibromochloronitromethane | Dibromochloronitromethane is one of Halonitromethanes, which are a recently identified class of disinfection by-products (DBPs) in drinking water. | |||||||||||||||||||||
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Tribromonitromethane | Tribromonitromethane is one of Halonitromethanes, which are a recently identified class of disinfection by-products (DBPs) in drinking water. | |||||||||||||||||||||
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Abrucomstat | 95.0% | Abrucomstat (3-Nitroxypropanol) is an orally active methyl coenzyme M reductase inhibitor. Abrucomstat decreases ruminal methanogenesis. | ||||||||||||||||||||
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THAM | 99.88% | THAM (Tris) is a low-toxicity amino alcohol buffer, a specific CO2-consuming proton acceptor that buffers carbon dioxide and acid both in vitro and in vivo. THAM binds protons to form bicarbonate, reduces PaCO2, and induces intracellular alkalization, thereby ameliorating hypercapnia-induced elevation of pulmonary blood vessels and pulmonary arterial pressure. THAM may cause PaCO2 rebound, hypoglycemia, and respiratory depression. THAM removes amniotic epithelium and preserves the basement membrane, but depletes extracellular matrix and reduces the adhesion rate of limbal epithelial cells. THAM can act as a CO2 carrier to enhance the productivity and carbon utilization rate of Scenedesmus obliquus. THAM is a key component of buffer solutions used in various biological, cell culture, biochemical, and molecular biology applications. | ||||||||||||||||||||
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THAM acetate | 97.0% | THAM acetate is a low-toxicity amino alcohol buffer, a CO2-consuming proton acceptor that buffers carbon dioxide and acid both in vitro and in vivo. THAM acetate binds protons to form bicarbonate, reduces PaCO2, and induces intracellular alkalization, thereby ameliorating hypercapnia-induced elevation of pulmonary blood vessels and pulmonary arterial pressure. THAM acetate may cause PaCO2 rebound, hypoglycemia, and respiratory depression. THAM acetate removes amniotic epithelium and preserves the basement membrane, but depletes extracellular matrix and reduces the adhesion rate of limbal epithelial cells. THAM acetate can act as a CO2 carrier to enhance the productivity and carbon utilization rate of Scenedesmus obliquus. THAM acetate is a key component of buffer solutions used in various biological, cell culture, biochemical, and molecular biology applications. | ||||||||||||||||||||
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THAM hydrochloride (≥99%, reagent grade) | 99.80% | THAM hydrochloride (≥99%, reagent grade), also known as Tris-HCl, is a buffer commonly used in various biochemical and molecular biology applications to maintain a stable pH environment. Tris-HCl has unique chemical properties that allow it to resist changes in pH when acidic or basic substances are added, which makes it useful for stabilizing biological samples or reagents. It is commonly used in electrophoresis and protein purification procedures. | ||||||||||||||||||||
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3-Nitropropanoic acid | 99.94% | 3-Nitropropanoic acid (β-Nitropropionic acid) is an irreversible and orally active inhibitor of succinate dehydrogenase. 3-Nitropropanoic acid exhibits potent antimycobacterial activity with a MIC value of 3.3 μM. 3-Nitropropanoic acid can induce cell apoptosis. | ||||||||||||||||||||
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2-Amino-2-methyl-1,3-propanediol | 98.0% | 2-Amino-2-methyl-1,3-propanediol is a solid-solid phase change material with energy release and heat storage properties. 2-Amino-2-methyl-1,3-propanediol can crystallize from a supercooled solid state, release thermal energy during heating, and store thermal energy in the supercooled solid state. 2-Amino-2-methyl-1,3-propanediol can be used in the production of surfactants, vulcanization accelerators, and as a biological buffer. | ||||||||||||||||||||
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Tris(hydroxymethyl)nitromethane | Tris (hydroxymethyl) nitromethane is a fungicide and slime control agent. Tris (hydroxymethyl) nitromethane exhibits cytotoxicity against EBV-transformed human Burkitt's lymphoma cells. Tris (hydroxymethyl) nitromethane also serves as an important raw material and intermediate in organic synthesis. | |||||||||||||||||||||
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References
- [2]. Kireche M, et al., Evidence for chemical and cellular reactivities of the formaldehyde releaser bronopol, independent of formaldehyde release. Chem Res Toxicol. 2011 Dec 19;24(12):2115-28. [Content Brief]
- [3]. Nieminen L, et al., The pain aggression induced by bronopol in the rat. Acta Pharmacol Toxicol (Copenh). 1975 Sep;37(3):237-41. [Content Brief]
