HEPTAMINOL ACEPHYLLINATE
Flammability | 1 | |
Toxicity | 2 | |
Body Contact | 1 | |
Reactivity | 1 | |
Chronic | 0 | |
SCALE: Min/Nil=0 Low=1 Moderate=2 High=3 Extreme=4 |
Theophylline derivative used as a muscle relaxant in diseases of the cardiovascular
system, asthma, bronchopneumonia, bronchitis and cardiac, pulmonary or renal oedema.
C8-H19-N-O.C9-H10-N4-O4, C8-H19-N-O.C9-H10-N4-O4, "heptaminol theophylline ethanoate",
"heptaminol theophylline-7-acetate", "heptaminol theophylline-7-acetate", "6-amino-2-
methylheptan-2-ol salt of theophyllin-7-ylacetic acid", "6-amino-2-methylheptan-2-ol salt
of theophyllin-7-ylacetic acid", "muscle relaxant"
None
Although ingestion is not thought to produce harmful effects, the material may still be damaging to the health of the individual following ingestion, especially where pre- existing organ (e.g. liver, kidney) damage is evident. Present definitions of harmful or toxic substances are generally based on doses producing mortality (death) rather than those producing morbidity (disease, ill-health). Gastrointestinal tract discomfort may produce nausea and vomiting. In an occupational setting however, ingestion of insignificant quantities is not thought to be cause for concern. Xanthine derivatives may produce nausea, vomiting, anorexia, stomach pain, vomiting of blood and diarrhea. Protein in the urine, increased amounts of urine output, and increased excretion of renal tubular cells and red blood cells may also occur. Effects on breathing may include increased rate and stoppage. Central nervous system effects may include restlessness, dizziness, headache, sleep disturbance, very brisk reflexes, stammering speech, muscle twitches and convulsions alternating with severe depression. Overdose can cause coma. Cardiovascular effects include palpitations, low blood pressure, fast heart rate, extra contractions, life-threatening irregularities of the ventricles and failure of circulation. Other symptoms of overexposure include rash, fever, flushing, high blood sugar, inappropriate secretion of antidiuretic hormone, and relaxation of the smooth muscle of the airways.
Although the material is not thought to be an irritant, direct contact with the eye may produce transient discomfort characterized by tearing or conjunctival redness (as with windburn). The dust may produce eye discomfort causing smarting, pain and redness.
The material is not thought to produce adverse health effects or skin irritation following contact (as classified using animal models). Nevertheless, good hygiene practice requires that exposure be kept to a minimum and that suitable gloves be used in an occupational setting.
The material is not thought to produce adverse health effects or irritation of the respiratory tract (as classified using animal models). Nevertheless, good hygiene practice requires that exposure be kept to a minimum and that suitable control measures be used in an occupational setting. Persons with impaired respiratory function, airway diseases and conditions such as emphysema or chronic bronchitis, may incur further disability if excessive concentrations of particulate are inhaled.
Principal routes of exposure are by accidental skin and eye contact andinhalation of generated dusts. Activity is mediated through inhibition of phosphodiesterase with a resulting increase in intracellular cyclic adenosine phosphate (cyclic AMP). The substance may be foetotoxic.