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  2. Butyric acid - Wikipedia

    en.wikipedia.org/wiki/Butyric_acid

    Butyric acid (/ ˈ b j uː t ɪ r ɪ k /; from Ancient Greek: βούτῡρον, meaning "butter"), also known under the systematic name butanoic acid, is a straight-chain alkyl carboxylic acid with the chemical formula CH 3 CH 2 CH 2 COOH. It is an oily, colorless liquid with an unpleasant odor. Isobutyric acid (2-methylpropanoic acid) is an ...

  3. Body odor - Wikipedia

    en.wikipedia.org/wiki/Body_odor

    These smaller molecules smell, and give body odor its characteristic aroma. [10] Propionic acid (propanoic acid) is present in many sweat samples. This acid is a breakdown product of some amino acids by propionibacteria, which thrive in the ducts of adolescent and adult sebaceous glands.

  4. Isovaleric acidemia - Wikipedia

    en.wikipedia.org/wiki/Isovaleric_acidemia

    Isovaleric acidemia has an autosomal recessive pattern of inheritance.. The disorder has an autosomal recessive inheritance pattern, which means the defective gene is located on an autosome, and two copies of the gene – one from each parent – must be inherited to be affected by the disorder.

  5. Biochemistry of body odor - Wikipedia

    en.wikipedia.org/wiki/Biochemistry_of_body_odor

    There are three types of sweat glands: eccrine, apocrine, and apoeccrine. [1] Apocrine glands are primarily responsible for body malodor and, along with apoeccrine glands, are mostly expressed in the axillary (underarm) regions, whereas eccrine glands are distributed throughout virtually all of the rest of the skin in the body, although they are also particularly expressed in the axillary ...

  6. Isovaleric acid - Wikipedia

    en.wikipedia.org/wiki/Isovaleric_acid

    Isovaleric acid, also known as 3-methylbutanoic acid or β-methylbutyric acid, is a branched-chain alkyl carboxylic acid with the chemical formula (CH 3) 2 CHCH 2 CO 2 H. It is classified as a short-chain fatty acid. Like other low-molecular-weight carboxylic acids, it has an unpleasant odor. The compound occurs naturally and can be found in ...

  7. Organic acidemia - Wikipedia

    en.wikipedia.org/wiki/Organic_acidemia

    Most of the organic acidemias result from defective autosomal genes for various enzymes important to amino acid metabolism.Neurological and physiological harm is caused by this impaired ability to synthesize a key enzyme required to break down a specific amino acid, or group of amino acids, resulting in acidemia and toxicity to specific organs systems.

  8. n-Butyl lactate - Wikipedia

    en.wikipedia.org/wiki/N-Butyl_lactate

    n-Butyl lactate reacts with strong acids, strong bases, and oxidizers.It is also flammable. Exposure to dangerous amounts can occur through inhalation, ingestion, skin contact, or eye contact and causes irritation of the affected area, drowsiness, headache, central nervous system depression, nausea, and vomiting. [1]

  9. Propionic acidemia - Wikipedia

    en.wikipedia.org/wiki/Propionic_acidemia

    This in turn causes an accumulation of dangerous acids and toxins, which can cause damage to the organs. [citation needed] In many cases, propionic acidemia can damage the brain, heart, kidney, liver, cause seizures and delays to normal development such as walking or talking.