ChemicalBook > Product Catalog > Chemical pesticides > Germicide > Other germicides > 2-Bromo-2-nitro-1,3-propanediol
2-Bromo-2-nitro-1,3-propanediol Chemical Properties
- Melting point:130-133 °C(lit.)
- Boiling point:358.0±42.0 °C(Predicted)
- Density 2.0002 (rough estimate)
- refractive index 1.6200 (estimate)
- Flash point:167°C
- solubility H2O: soluble100mg/mL, clear, colorless to faintly yellow
- form Crystals or Crystalline Powder
- color White to yellow
- Water Solubility 25 g/100 mL (22 ºC)
- Merck 14,1447
- BRN 1705868
- Stability:Stable. Hygroscopic. Incompatible with strong oxidizing agents, strong bases, strong reducing agents, acid chlorides and anhydrides, moisture.
- CAS DataBase Reference52-51-7(CAS DataBase Reference)
- NIST Chemistry ReferenceBronopol(52-51-7)
- EPA Substance Registry SystemBronopol (52-51-7)
- Hazard Codes Xn,N
- Risk Statements 21/22-37/38-41-50
- Safety Statements 26-37/39-61-36/37/39
- RIDADR UN 3241 4.1/PG 3
- WGK Germany 2
- RTECS TY3385000
- F 4.2-8-9-21
- TSCA Yes
- HazardClass 4.1
- PackingGroup III
- HS Code 29055999
- Hazardous Substances Data52-51-7(Hazardous Substances Data)
- ToxicityLD50 in mice, rats (mg/kg): 350, 400 orally (Croshaw)
2-Bromo-2-nitro-1,3-propanediol Usage And Synthesis
- Chemical Propertiesoff-white crystalline powder
- Chemical PropertiesBronopol is a white or almost white crystalline powder; odorless or with a faint characteristic odor.
- UsesPreservative in cosmetics and toiletries. Antiseptic.
- Production MethodsBronopol is synthesized by the reaction of nitromethane with paraformaldehyde in an alkaline environment, followed by bromination. After crystallization, bronopol powder may be milled to produce a powder of the required fineness.
- General DescriptionWhite crystals. Ignite easily and burn readily. May detonate under strong shock. Decomposes when heated, evolving toxic gases. Toxic by skin absorption, inhalation or ingestion.
- Air & Water ReactionsHighly flammable. Water soluble.
- Reactivity ProfileIncompatible with strong oxidizing agents, strong bases, strong reducing agents, acid chlorides and acid anhydrides. 2-Bromo-2-nitro-1,3-propanediol is also incompatible with sulfhydryl compounds or with aluminum or iron containers (it is stable in contact with tin or stainless steel).
- HazardToxic by all routes of exposure; skin irritant.
- Health HazardFire may produce irritating and/or toxic gases. Contact may cause burns to skin and eyes. Contact with molten substance may cause severe burns to skin and eyes. Runoff from fire control may cause pollution.
- Fire HazardFlammable/combustible material. May be ignited by friction, heat, sparks or flames. Some may burn rapidly with flare burning effect. Powders, dusts, shavings, borings, turnings or cuttings may explode or burn with explosive violence. Substance may be transported in a molten form at a temperature that may be above its flash point. May re-ignite after fire is extinguished.
- Pharmaceutical ApplicationsBronopol 0.01–0.1% w/v is used as an antimicrobial preservative either alone or in combination with other preservatives in topical pharmaceutical formulations, cosmetics, and toiletries; the usual concentration is 0.02% w/v.
- Contact allergensBronopol is a preservative sometimes considered as a formaldehyde releaser. It was reported to be an allergen in cosmetics, cleaning agents, dairy workers, and a lubricant jelly used for ultrasound examination.
- Safety ProfilePoison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Moderately toxic by skin contact. An eye and human skin irritant. An antiseptic. When heated to decomposition it emits very toxic fumes of NOx, and Br-.
- SafetyBronopol is used widely in topical pharmaceutical formulations and
cosmetics as an antimicrobial preservative.
Although bronopol has been reported to cause both irritant and hypersensitivity adverse reactions following topical use, it is generally regarded as a nonirritant and nonsensitizing material at concentrations up to 0.1% w/v. At a concentration of 0.02% w/v, bronopol is frequently used as a preservative in ‘hypoallergenic’ formulations.
Animal toxicity studies have shown no evidence of phototoxicity or tumor occurrence when bronopol is applied to rodents topically or administered orally; and there is no in vitro or in vivo evidence of mutagenicity; this is despite the demonstrated potential of bronopol to liberate nitrite on decomposition, which in the presence of certain amines may generate nitrosamines. Formation of nitrosamines in formulations containing amines may be reduced by limiting the concentration of bronopol to 0.01% w/v and including an antioxidant such as 0.2% w/v alpha tocopherol or 0.05% w/v butylated hydroxytoluene;(14) other inhibitor systems may also be appropriate.
LD50 (dog, oral): 250 mg/kg
LD50 (mouse, IP): 15.5 mg/kg
LD50 (mouse, IV): 48 mg/kg
LD50 (mouse, oral): 270 mg/kg
LD50 (mouse, SC): 116 mg/kg
LD50 (mouse, skin): 4.75 g/kg
LD50 (rat, IP): 26 mg/kg
LD50 (rat, IV): 37.4 mg/kg
LD50 (rat, oral): 180 mg/kg
LD50 (rat, SC): 170 mg/kg
LD50 (rat, skin): 1.6 g/kg
- storageBronopol is stable and its antimicrobial activity is practically
unaffected when stored as a solid at room temperature and ambient
relative humidity for up to 2 years.
The pH of a 1.0% w/v aqueous solution is 5.0–6.0 and falls slowly during storage; solutions are more stable in acid conditions.
Microbiological assay results indicate longer half-lives than those obtained by HPLC and thus suggest that degradation products may contribute to antimicrobial activity. Formaldehyde and nitrites are among the decomposition products, but formaldehyde arises in such low concentrations that its antimicrobial effect is not likely to be significant. On exposure to light, especially under alkaline conditions, solutions become yellow or brown-colored but the degree of discoloration does not directly correlate with loss of antimicrobial activity.
The bulk material should be stored in a well-closed, nonaluminum container protected from light, in a cool, dry place.
- IncompatibilitiesSulfhydryl compounds cause significant reductions in the activity of bronopol, and cysteine hydrochloride may be used as the deactivating agent in preservative efficacy tests; lecithin/polysorbate combinations are unsuitable for this purpose. Bronopol is incompatible with sodium thiosulfate, with sodium metabisulfite, and with amine oxide or protein hydrolysate surfactants. Owing to an incompatibility with aluminum, the use of aluminum in the packaging of products that contain bronopol should be avoided.
- Regulatory StatusIncluded in topical pharmaceutical formulations licensed in Europe. Included in the Canadian List of Acceptable Non-medicinal Ingredients.
2-Bromo-2-nitro-1,3-propanediol Preparation Products And Raw materials
- 3-BROMO-3-NITRO-2,4-PENTANEDIOL 5-Bromo-5-nitro-1,3-dioxane 2-BROMO-2-NITRO-3-[(2-THIENYLCARBONYL)OXY]PROPYL THIOPHENE-2-CARBOXYLATE 2-BROMO-2-NITRO-3-([3-(TRIFLUOROMETHYL)BENZOYL]OXY)PROPYL 3-(TRIFLUOROMETHYL)BENZOATE nibroxane 2-BROMO-3-[(4-CHLOROBENZOYL)OXY]-2-NITROPROPYL 4-CHLOROBENZOATE 2-Bromo-2-nitro-1,3-propanediol Isopropyl alcohol 1,3-Propanediol p-Nitrobenzoic acid 1-Propanol Nitromethane Nitrobenzene NITROGEN DIOXIDE 1-Phenyl-2-nitropropene Bromine 2,4,6-TRINITROTOLUENE Triisopropanolamine
- Company Name:Alfa Aesar Gold
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- Company Name:Weifang Kaihong Chemical Limited Gold
- Company Name:Shanghai SMEC Trading Co., Ltd. Gold
- Company Name:Wuhan Mengqi Technology Co., Ltd. Gold
- Company Name:Hubei Xingyinhe Chemical Co., Ltd. Gold