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CHEMICAL HAZARDS 219
respiratory, cardiac, central, and peripheral nervous systems, as well as liver and kidney function. Alcohol intake should be evaluated.
SPECIAL TESTS Expired air analysis and urinary metabolites have been used to
monitor exposure.
PERSONAL PROTECTIVE METHODS Gloves and protective clothing should be worn, and fullface mask
should be used in areas of excessive vapor concentrations.
BIBLIOGRAPHY Bauer, M., and S. F. Rabene 1974. Cutaneous manifestations of trichloroethylene
toxicity. Arch. Derm. 110:886. Feldman, R. G., R. M. Mayer, and A. Traub. 1970. Evidence for peripheral
neurotoxic effect of trichloroethylene. Neurology 20:599. Lloyd, J. W,, R. M. Moore, Jr., and P. Breslin. 1975. Background information on
trichloroethylene. J. Occup. Med. 17:603. Lowry, L. K., R. Vandervort. and P. L. Polakoff. 1974. Biological indicators of
occupational exposure to trichloroethylene. Occup. Med. 16:98. Pardys, S,, and M. Brotman. 1974. Trichloroethylene and alcohol: a straight flush.
J. Am. Med. Assoc. 229:521.
VINYL CHLORIDE
DESCRIPTION CH, = CHCI, vinyl chloride, is a flammable gas at room tempera
ture and is usually encountered as a cooled liquid. The colorless liquid forms a vapor which has a pleasant ethereal odor.
SYNONYMS Chloroethylene, chloroethene, monochloroethylene.
POTENTIAL OCCUPATIONAL EXPOSURES Vinyl chloride is used as a vinyl monomer in the manufacture of
polyvinyl chloride and other resins. It is also used as a chemical inter mediate and as a solvent.
A partial list of occupations in which exposure may occur includes: Polyvinyl resin makers Organic chemical synthesizers Rubber makers
PERMISSIBLE EXPOSURE LIMITS The Federal standard for exposure to vinyl chloride sets a limit of
1 ppm over an 8-hour period, and a ceiling of 5 ppm averaged over any period not exceeding 15 minutes.
ROUTES of ENTRY Vinyl chloride ga;, i$ absorbed hv inhalation. Skin absorption has
tn suggested but experimental evidence is presently lacking.
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HARMFUL EFFECTS
Local--
Vinyl chloride is a skin irritant, and contact with the liquid may cause frostbite upon evaporation. The eyes may be immediately and severely irritated.
Systemic--
Vinyl chloride depresses the central nervous system causing symp toms which resemble mild alcohol intoxication. Lightheadedness, some nausea, and dulling of visual and auditory responses may develop in acute exposures. Death from severe vinyl chloride exposure has been reported.
Chronic exposure of workers involved in reactor vessel entry and hand cleaning may result in the triad of acro-osteolysis, Raynaud's phe nomenon, and sclerodermatus skin changes. Chronic exposure may also cause hepatic damage.
VjjpYl fbloride is regarded as p human carcinogen, and a causal agent trf angiosarcoma of the liver. Excess canceV'ofthe lung and tfie tympliatic'anir^nervous systems lias also been reported. Experimental evidence of tumor induction in a variety of organs, including liver, lung, brain, and kidney, as well as nonmalignant alterations, such as fibrosis and connective tissue deterioration, indicate the multisystem oncogenic and toxicologic effects of vinyl chloride.
MEDICAL SURVEILLANCE
Preplacement and periodic examinations should emphasize liver function and palpation. Liver scans and grey-scale ultrasonography have been useful in detecting liver tumors. Medical histories should include alcoholic intake; past hepatitis; exposure to hepatotoxic agents, drugs and chemicals; past blood transfusions; past hospitalizations. Radiographic examinations of the hands may be helpful if acroosteolysis is suspected. Long term followup, of exposed persons is essential as in the case of other carcinogens.
SPECIAL TESTS
None in common use. Metabolism is being studied.
PERSONAL PROTECTIVE METHODS Where vinyl chloride levels cannot meet the standard, workers
should be required to wear respiratory protection, either air supplied respirator or, if the level does not exceed 25 ppm, a chemical cartridge or cannister type gas mask. In hazard areas, proper protective clothing to prevent skin contact with the vinyl chloride or polyvinyl chloride residue should be worn.
BIBLIOGRAPHY
Berk, P. D,, J. F. Martin, R. S. Young, J. Creech, I. I. Selikoff, H. Falk P Watanabe, H. Popper, and L. Thomas. 1976. Vinyl chloride-associated liver diseases. Ann. Intern. Med. 84:717.
X>dson, V. N,, B. D. D Magnuson. 1971. O Environ. Health 22:1
Duck, B. W. 1976. Medr Med. 69:307.
Editorial: Vinyl chloride: Falk, H,, J. L. Creech, J
1974. Hepatic diseas I, Am. Med. Assoc Fox, A. J.. and P. F. O vinyl chloride mont Britain. Brit. J. Ind. Haley, T. J. 1975. Vin; anj Environ. Dealt!
eston. B. J., K. Lloy
Taylor, K. J. W., D. M scale ultrasonogra agents. Lancet 1:12
Viola, P. L. 1970. Par Waxweiller, R. J., W. S
among workers ex
ALIPHATIC AP
The aliphatic one or more hydro* They tend to have base form.
These compou or hydrogenation c industry, particular
The amines a: solutions which ca with eyes and skin, able of cutaneous : physiologic or ph vasodilation, but, i posures.
Because of th skin, and respirator
N-BVTYLAM1
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CHEMICAL HAZARDS 221
Dodson, V. N., B. D, Dinman, W. M, Whitehouse, A, H. M. Nasr, and H. J. Magnuson. 1971. Occupational acro-osteolysis: III. A clinical study. Arch. Environ. Health 22:83.
Duck, B. W. 1976. Medical surveillance of vinyl chloride workers. Proc. R. Soc. Med. 69:307.
Editorial: Vinyl chloride: the carcinogenic risk. 1976. Brit. Med. J. 2:134. Falk, H., J. L. Creech, Jr., C. W. Heath, Jr., M. N. Johnson, and M. M. Key.
1974. Hepatic disease among workers at a vinyl chloride polymerization plant. J. Am. Med. Assoc. 230;J9. Fox, A. J., and P. F. Collier. 1977. Mortality experience of workers exposed to vinyl chloride monomer in the manufacture of polyvinyl chloride in Great Britain. Brit. J. Ind. Med. 34:1. Haley, T. J. 1975. Vinyl chloride: How many unknown problems? J. Toxicol, and Environ. Health 1:47. Makk, L., J. L. Creech, J. G. Whelan, and M. N. Johnson. 1974. Liver damage and angiosarcoma in vinyl chloride workers: a systematic detection program. J. Am. Med. Assoc. 230:64,
Preston, B. J., K- Lloyd Jones, and R. G. Grainger. 1976. Clinical aspects of vinyl chloride disease. Proc. R. Soc. Med. 69:284.
Selikoff, I. J., and E. C. Hammond, eds. 1975. Toxicity of vinyl chloride-polyvinyl chloride. Ann. N. V. Acad, Sci. 246:1.
Taylor, K. J. W., D. M. J. Williams, P. M. Smith, and B. W. Duck. 1975. Grey scale ultrasonography for monitoring industrial exposure to hepatotoxic agents. Lancet 1:1222.
Viola, P. L. 1970. Pathology of vinyl chloride. Med. Lav. 61:174. Waxweiller, R. J., W. Stringer, J. K. Wagoner, and J, Jones. 1976. Neoplastic risk
among workers exposed to vinyl chloride. Ann. N.Y. Acad. Sci. 271:40.
ALIPHATIC AMINES
The aliphatic amities are derivatives of ammonia (NH3) in which one or more hydrogen atoms are replaced by alkyl or alkanol radicals. They tend to have a characteristic fishlike ammonia odor in the free base form.
These compounds are generally prepared by alkylation of ammonia or hydrogenation of the appropriate nitrite. They are widely used in industry, particularly as chemical intermediates.
The amines are basic compounds and may form strongly alkaline solutions which can be highly irritating and cause damage on contact with eyes and skin. Skin absorption may be significant as many are cap able of cutaneous sensitization. Some members of this series may have physiologic or pharmacologic effects--e g., histamine liberation and vasodilation, but, in genera), local effects predominate in industrial ex posures.
Because of the strong irritant properties of aliphatic amines, eyes, skin, and respiratory tract should be protected from exposure to them.
N-BUTYLAM1NE
description
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CHj-CH.-CH,-Cn-butylamine, is a flammable colorle s liquid with an ammoniacal odor.
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