Weight | 199.988 g/mol |
---|---|
Formula | C3H6BrNO4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
bronopol (52-51-7)
2-bromo-2-nitro-1,3-propanediol · bronosol
Score:
#72 in Microbiology
,
#948 in Biology
,
#1049 in Chemistry
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- Antibacterial properties of plasma-modified and triclosan or bronopol coated polyethylene (Polymer, 2006)
- Antibacterial action of 2-bromo-2-nitropropane-1,3-diol (bronopol). (Antimicrobial Agents and Chemotherapy, 1988)
- Some Aspects of the Mode of Action of the Antibacterial Compound Bronopol (2-bromo-2-nitropropan-1,3-diol) (Journal of Applied Microbiology, 1973)
- SOME PROPERTIES OF BRONOPOL, A NEW ANTIMICROBIAL AGENT ACTIVE AGAINST PSEUDOMONAS AERUGINOSA. (Journal of Pharmacy and Pharmacology, 1964)
- Reactions to Quaternium 15, Bronopol and Germall 115 in a standard series (Contact Dermatitis, 1986)
- The activity and safety of the antimicrobial agent bronopol (2-bromo-2-nitropropan-1, 3-diol) (1978)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H228: Flammable solid
Warning Flammable solids - Category 2 - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H335: May cause respiratory irritation
Warning Specific target organ toxicity, single exposure; Respiratory tract irritation - Category 3 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - 2-bromo-2-nitro-1,3-propanediol
- bronosol
-
SMILESC(C(CO)([N+](=O)[O-])Br)O
-
InChIKeyLVDKZNITIUWNER-UHFFFAOYSA-N
- Pubchem - bronopol
- Wikipedia - bronopol
Bronopol (INN) is an organic compound that is used as an antimicrobial. It is a white solid although commercial samples appear yellow. The first cited synthesis of 2-Bromo-2-nitro-1,3-propanediol is 1897 according to Molbase.
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