Cosmetic Antiseptic Bronopol Fungicide 2-Bromo-2-Nitro-1,3-Propanediol

Product Details
Place of Origin: WEIFANG,CHINA
Brand Name: ZHAOYU
Certification: ISO 9001; ISO 45001; ISO 14001
Model Number: 99.0%
Payment & Shipping Terms
Minimum Order Quantity: 500 kgs
Price: Negotiatable
Packaging Details: 25kg Cardboard barrel; 500kg Container bag
Delivery Time: 15 work days
Supply Ability: 2000 Tons/Year

Detail Information

Place of Origin WEIFANG,CHINA Brand Name ZHAOYU
Certification ISO 9001; ISO 45001; ISO 14001 Model Number 99.0%
Another Name:: Bronopol、BNPD Chemical Name:: 2-Bromo-2-Nitro-1,3-Propanediol
Molecular Formula:: C3H6BrNO4 Molecular Weight:: 199.988
CAS NO.:: 52-51-7 Einecs NO.:: 200-143-0
Content:: 99.0% Min Moisture:: 0.5% Max
Appearance:: White To Light Yellow Crystalline Powder Melting Point:: 129-132℃
Stability:: Slightly Hygroscopic High Light:

ISO14001 Bronopol Fungicide

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ISO14001 Bronopol In Cosmetics

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Bronopol Fungicide Compound

Product Description

Physical and chemical properties: The content of pure product is 99% (the content of aldehyde is 30%), and the appearance is white to light yellow powder or crystal. The melting point is 130°C. Vapor pressure (20°C) 1.68mPa. Solubility: water 250g/L (22°C); ethanol 500g/L, isopropanol 250g/L, propylene glycol 143g/L, glycerin 10g/L, liquid paraffin <5g/L (23~24°C). Stability: slightly hygroscopic.

Mechanism of antibacterial and antifungal effect: Bronopol has bactericidal effect through different chemical reaction mechanisms in aerobic and anaerobic atmospheres. In an aerobic atmosphere, bronopol catalyzes the oxidation of cysteine amino acids to cystine residues (Shepher et al., 1988). This mechanism is thought to act to kill microorganisms through the formation of reactive oxygen species such as superoxide or peroxide. Moreover, the formed cystine residues are attached to the cell wall, preventing the normal formation of the cell wall. The formation of reactive oxygen species and the cross-linking of cystine residues with the cell wall jointly lead to cell death. In an oxygen-free environment, the mechanism is that cells and extracellular nucleophiles attack the No. 2 carbon atom in the bronopol molecule.

The compound has good bactericidal and antibacterial effects on Gram-positive bacteria, Gram-negative bacteria, molds and yeasts, and is particularly effective on Pseudomonas aeruginosa.

 

Application: In 1919, bronopol was prepared by R.Wilkendorf, and then the British Pharmaceutical Association announced its general name Bromopol. This biocide is mainly used in industrial circulating water, paper pulp, coatings, plastics, cosmetics, wood, and cooling water circulation systems And other fields including agriculture, sterilization, anti-corrosion and anti-algae. Note: ① Due to the good stability of bronopol in acidic solutions, weakly acidic media are ideal for field applications. ② Exposure to light may make the product yellow, sensitive to iron and aluminum packaging materials, and reacts with amines and alkaline compounds. ③flammable. Produces irritating or toxic fumes (or gases) in a fire, including hydrogen bromide and nitrogen oxides.

2-Bromo-2-Nitro-1,3-Propanediol (Bronopol)

Cosmetic Antiseptic Bronopol Fungicide 2-Bromo-2-Nitro-1,3-Propanediol 0

 

Product Name 2-Bromo-2-Nitro-1,3-Propanediol (Bronopol)
Molecular Formula C3H6BrNO4
Molecular Weight 199.988
CAS NO. 52-51-7
Appearance White to light yellow crystalline powder
Content 99.0% min
Melting Point 129-132℃
Moisture 0.5% max

 

Cosmetic Antiseptic Bronopol Fungicide 2-Bromo-2-Nitro-1,3-Propanediol 1

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