| Weight | 446.591 g/mol |
|---|---|
| Formula | C28H34N2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 8 |
DENATONIUM BENZOATE (3734-33-6)
Bitrex
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LabBot
- Effectiveness of capsaicin and bitrex repellents for deterring browsing by captive mule deer (Journal of Wildlife Management, 1994)
- Bittering agents in the prevention of accidental poisoning: children's reactions to denatonium benzoate (Bitrex). (Emergency Medicine Journal, 1991)
- Research on the Effectiveness of Denatonium Benzoate as a Deterrent to Liquid Detergent Ingestion by Children (Toxicological Sciences, 1982)
- Denatonium benzoate as a deterrent to ingestion of toxic substances: toxicity and efficacy. (Veterinary and Human Toxicology, 1993)
- Denatonium benzoate: review of efficacy and safety. (Veterinary and Human Toxicology, 1991)
- EVALUATIONS OF AVERSIVE AGENTS TO INCREASE THE SELECTIVITY OF RODENTICIDES, WITH EMPHASIS ON DENATONIUM BENZOATE (BITREX) BITTERIN G AGENT (1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Bitrex
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SMILESCC[N+](CC)(CC1=CC=CC=C1)CC(=O)NC2=C(C=CC=C2C)C.C1=CC=C(C=C1)C(=O)[O-]
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InChIKeyVWTINHYPRWEBQY-UHFFFAOYSA-N
- Pubchem - DENATONIUM BENZOATE
- Wikipedia - denatonium benzoate anhydrous
Denatonium, usually available as denatonium benzoate (under trade names such as BITTERANT-b, BITTER+PLUS, Bitrex or Aversion) and as denatonium saccharide (BITTERANT-s), is the most bitter chemical compound known, with bitterness thresholds of 0.05 ppm for the benzoate and 0.01 ppm for the saccharide. It was discovered in 1958 during research on local anesthetics by MacFarlan Smith of Edinburgh, Scotland, and registered under the trademark Bitrex. Dilutions of as little as 10 ppm are unbearably bitter to most humans.
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DENATONIUM BENZOATE
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