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Rhode Island Hazardous Substance List

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Rhode Island Hazardous Substance List Source: T - ACGIH F - NFPA49 C - IARC Alphabetical Order C.A.S. ACGIH NFPA IARC CHEMICAL NAME 13010-47-4 C 1,-(2-Chloroethyl)-3-cyclohexyl-1-Nitrosourea 76-11-9 T 1,1,1,2-tetrachloro-2,2-difluoroethane 76-12-0 T 1,1,2,2-tetrachloro-1,2-difluoroethane 79-34-5 T 1,1,2,2-tetrachloroethane - skin 76-13-1 T 1,1,2-trichloro-1,2,2-trifluoroethane 79-00-5 T F C 1,1,2-trichloroethane - skin 594-72-9 T 1,1-Dichloro-1-nitroethane 74-34-3 T 1,1-dichloroethane 57-14-7 T 1,1-dimethylhydrazine (udmh) 96-18-4 T 1,2,3-trichloropropane 120-82-1 T 1,2,4-Trichlorobenzene 106-88-7 F 1,2-Butylene oxide 107-15-3 T F 1,2-Diaminoethane 96-12-8 C 1,2-Dibromo-3-chloropropane 106-93-4 T F C 1,2-Dibromoethane - skin 107-06-2 T F 1,2-Dichlorethane 540-59-0 T F 1,2-Dichloroethene 540-59-0 T F 1,2-Dichloroetylene 1615-80-1 C 1,2-Diethylhydrazine C 1,2-Dimethyl hydrazine - skin 106-99-0 T F 1,3-Butadiene 118-52-5 T 1,3-Dichloro-5,5-dimethylhydantoin 542-75-6 T F 1,3-Dichloropropene (cis and trans) 542-75-6 T F 1,3-Dichloropropylene 110-56-5 F 1,4-Dichlorobutane 123-91-1 T F C 1,4-Dioxane 1120-71-4 1-3-Propane sultone 110-53-2 F 1-Bromopentane 106-89-8 T F C 1-Chloro,2,3-epoxy-propane 600-25-9 T 1-Chloro-1-nitropropane 97-00-7 F 1-chloro-2,4-dinitrobenzene 543-59-9 F 1-Chloropentane 112-30-1 F 1-Decanol 111-27-3 F 1-Hexanol 141-79-7 T F 1-Isobutenyl methyl ketone 108-03-2 T F 1-Nitropropane 71-41-0 F 1-Pentanol 110-58-7 F 1-Pentylamine 111-40-0 T F 2,2'-Diaminodiethylamine 111-44-4 F 2,2'Dichlorodiethyl ether 75-99-0 T 2,2-dichloropropionic acid 556-52-5 T 2,3-Epoxy-1-propanol 93-76-5 T 2,4,5-T 95-95-4 F 2,4,5-trichlorophenol 88-06-2 F C 2,4,6-trichlorophenol 118-96-7 T F 2,4,6-Trinitro Toluene 479-95-8 T 2,4,6-Trinitrophenyl-methylnitramine 94-75-7 T 2,4-d (2,4-dichlorophenoxyacetic acid) 97-02-9 F 2,4-dinitroaniline 584-84-9 T F 2,4-Tolylene diisocyanate 108-83-8 T 2,6-Dimethyl-4-heptanone 108-83-8 T 2,6-Dimethyl-4-heptanone 128-37-0 T 2,6-Ditert. butyl-p-cresol 141-43-5 T F 2-Aminoethanol 504-29-0 T 2-Aminopyridine 123-73-9 T F 2-Butenal 111-76-2 T 2-Butoxyethanol - skin 126-99-8 T 2-Chloro-1,3-butadiene 1929-82-4 T 2-Chloro-6-(trichloromethyl) pyridine 107-07-3 T 2-Chloroethanol 110-80-5 T 2-Ethoxyethanol - skin 111-15-9 T 2-Ethoxyethyl acetate - skin 97-95-0 F 2-ethylbutanol 123-66-0 F 2-Ethylbutyl acetate 103-11-7 F 2-Ethylhexyl acrylate 110-43-0 T 2-Heptanone 591-78-6 T 2-Hexanone 75-86-5 F 2-hydroxy-2-methylpropaneitrile 75-86-5 F 2-Hydroxy-2-methylpropanenitrile 141-43-5 T F 2-Hydroxyethylamine 999-61-1 T 2-Hydroxypropyl acrylate - skin 109-86-4 T 2-Methoxyethanol - skin 110-49-6 T 2-Methoxyethyl acetate - skin 75-85-4 F 2-methyl-2-butanol 75-69-4 F 2-methyl-2-propanol 108-10-1 T F 2-Methyl-4-pentanone 96-17-3 F 2-methylbutyraldehyde 102-81-8 T 2-N-Dibutylaminoethanol - skin 79-46-9 T F 2-nitropropane 6032-29-7 F 2-Pentanol 107-87-9 T 2-Pentanone 119-90-4 C 3,3' Dimethoxybenzidine 91-94-1 T C 3,3'-dichlorobenzidine - skin 119-93-7 T C 3,3'-Dimethylbenzidine 95-76-1 F 3,4-dichloroaniline 148-01-6 T 3,5-Dinitro-o-toluamide 2148-01-6 T 3,5-Dinitro-o-tolumide 106-95-6 F 3-Bromopropene-1 106-96-7 F 3-Bromopropyne 107-05-1 T F 3-Chloropropene 106-35-4 T F 3-Heptanone 109-78-4 F 3-Hydroxypropanenitrile 584-02-1 F 3-Pentanol 101-14-4 T 4,4'-Methylene bis(2-chloroaniline) - skin 101-77-9 T 4,4-Methylene dianiline - skin 96-69-5 T 4,4'-thiobis (6-tert-butyl-m-cresol) 92-67-1 T C 4-aminobiphenyl 123-42-2 T 4-Hydroxy-4-methyl-2-pentanone 150-76-5 T 4-Methoxyphenol 92-93-3 T 4-nitrobiphenyl 104-90-5 F 5-Ethyl-2-methylpyridine 104-90-5 F 5-Ethyl-2-picoline 541-85-5 T 5-Methyl-3-heptanone 194-59-2 C 7H-Dibenzo(c.g.)carbazone 3383-96-8 T Abate 75-07-0 T F acetaldehyde 64-19-7 T F acetic acid glacial 108-24-7 T F Acetic Anhydride 67-64-1 T F acetone 75-05-8 T F acetonitrile 98-86-2 F acetophenone 75-36-5 F acetyl chloride 110-22-5 F Acetyl peroxide 74-86-2 T F acetylene 540-59-0 T F Acetylene dichloride 79-27-6 T F acetylene tetrabromide 107-02-8 T F Acrolein 100-73-2 F Acrolein dimer 79-06-1 T acrylamide - skin 79-10-7 T F acrylic acid 107-13-1 T F C Acrylonitrile - skin 124-04-9 F Adipic acid 111-69-3 F Adiponitrile 23214-92-8 C Adriamycin 1402-68-2 C Aflatoxins 309-00-2 T F Aldrin -skin F Alkylaluminums 107-18-6 T F allyl alcohol - skin 106-95-6 F Allyl Bromide 107-05-1 T F Allyl chloride 2937-50-0 F Allyl Chlorocarbonate 2937-50-0 F Allyl chloroformate 106-92-3 T Allyl glycidyl ether (AGE) - skin 2179-59-1 T Allyl propyl disulfide 107-11-9 F Allylamine 1344-28-1 T alpha-Alumina 532-27-4 T alpha-Chloroacetophenone 100-44-7 T F alpha-Chlorotoluene 98-83-9 T alpha-methyl styrene 7429-90-5 T F Aluminum (Dust or Powder),metal & oxide, welding fumes, 7446-70-0 F Aluminum chloride (anhydrous) 1344-28-1 T Aluminum oxide - "inert" particulate 61-82-5 T C amitrole 7773-06-0 T Ammate 7664-41-7 T F Ammonia - anhydrous 7789-09-5 F Ammonium bichromate 12124-97-9 F Ammonium bromide 12125-02-9 T F Ammonium chloride - fume 7789-09-5 F Ammonium dichromate 12125-01-8 F Ammonium flouride 6484-52-2 F Ammonium nitrate 7790-98-9 F Ammonium perchlorate 13446-10-1 F Ammonium permanganate 7773-06-0 T Ammonium sulfamate 7783-20-2 F Ammonium sulfate 110-66-7 F Amyl mercaptans 1002-16-0 F Amyl nitrate 110-58-7 F Amylamine 62-44-2 C Analgesic mixtures containing phenacetin or phenecetin 62-53-3 T F aniline & homologues - skin 29191-52-4 T Anisidine (o-, p-, isomers) - skin 7440-36-0 T Antimony and compounds, as Sb. 7647-18-9 F Antimony Pentachloride 7783-70-2 F Antimony pentaflouride 1315-04-4 F Antimony pentasulfide 1315-04-4 F Antimony red 1309-64-4 T Antimony trioxide 86-88-4 T antu 140-57-8 C Aramite 7440-37-1 T Argon 7440-38-2 T C Arsenic and soluble compounds (as As) 7784-34-1 F Arsenic chloride 1327-53-3 T Arsenic trioxide production 1303-33-9 F Arsenic trisulfide 7784-34-1 F Arsenious chloride 7784-34-1 F Arsenous chloride 7784-42-1 T Arsine 1332-21-4 T C Asbestos 8052-42-4 T F Asphalt (petroleum) 50-78-2 T aspirin (acetylsalicylic acid) 1912-24-9 T Atrazine 492-80-8 C Auramine 115-02-6 C Azaserine 446-86-6 C Azathioprine 86-50-0 T azinphos-methyl - skin 151-56-4 T F Aziridine 6923-22-4 T Azodrin 13477-00-4 F Barium chlorate 10022-31-8 F Barium nitrate 1304-29-6 F Barium peroxide 7440-39-3 T Barium soluble compounds (as Ba) 1304-29-6 F Barium superoxide 114-26-1 T Baygon 55-63-0 T baytex 17804-35-2 T Benomyl 56-55-3 C Benz (a) anthacene 225-51-4 C Benz (c) acridine 100-52-7 F Benzaldehyde 71-43-2 T F C benzene - skin 100-52-7 F Benzenecarbonal 92-87-5 T C benzidine 205-99-2 C Benzo (b) fluoranthene C Benzo (j) fluoranthene 50-32-8 T benzo[a]pyrene 100-52-7 F Benzoic Aldehyde 98-08-8 F benzotriflouride 98-88-4 F benzoyl chloride 94-36-0 T F benzoyl peroxide 100-44-7 T F Benzyl chloride 7440-41-7 T F C Beryllium (as Be) 126-99-8 T beta-Chloroprene - skin 91-59-8 T C beta-Naphthylamine 57-57-8 T beta-propiolactone F Bichromates 141-66-2 T Bidrin 92-52-4 T biphenyl 54-28-8 C bis(chloromethyl)ether 154-93-8 C Bischloroethyl nitrosourea 542-88-1 T bis-Chloromethyl ether 1304-82-1 T Bismuth telluride 7778-54-3 F Bleaching powder 35400-43-2 T Bolstar 1303-96-4 T Borates, tetra, sodium salts 17702-41-9 T F Boron hydride (Decaborane) 19287-45-7 T F Boron hydride (Diborane) 1303-86-2 T Boron oxide 10294-33-4 T Boron tribromide 7637-07-2 T F Boron triflouride 314-40-9 T Bromacil 7726-95-6 T F Bromine 506-68-3 F Bromine Cyanide 7789-30-2 T F Bromine pentaflouride 7787-71-5 F Bromine triflouride 75-25-2 T bromoform - skin 55-98-1 C busulfan 106-99-0 T F Butadiene-1,3 123-72-8 F Butanal 106-97-8 T F Butane 109-79-5 T Butanethiol 107-92-6 F Butanoic acid 25167-67-3 F Butenes 109-79-5 T Butlyl mercaptan 7784-34-1 F Butter of arsenic 141-32-2 T F Butyl acrylate 136-60-7 F Butyl benzoate 111-76-2 T Butyl cellosolve 142-96-1 F Butyl ether 614-45-9 F Butyl Perbenzoate (tertiary) 107-71-1 F Butyl peroxyacetate, ter.(75% sol'n in benzene or mineral sp 927-07-1 F Butyl peroxypivalate (tert.) (75% sol'n in mineral spirits) 109-73-9 T F Butylamine - skin F Butyllithium in hydrocarbon solvents 123-72-8 F Butyraldehyde (normal and iso) 107-92-6 F Butyric acid (normal) 7440-43-9 T C Cadmium - dusts and salts - as Cd.
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  • 160 'Ideal' Gases: Anaesthetics in the Heart of the Twentieth Century Ian

    160 'Ideal' Gases: Anaesthetics in the Heart of the Twentieth Century Ian

    International Workshop on the History of Chemistry 2015 Tokyo ‘Ideal’ Gases: Anaesthetics in the Heart of the Twentieth Century Ian D. Rae University of Melbourne, Australia 1. Introduction By 1920 only three gaseous anaesthetics were widely used – nitrous oxide, diethyl ether (ether) and chloroform. The toxicity of chloroform was acknowledged, nitrous oxide did not induce deep anaesthesia, and ether was extremely inflammable, so in the 1920s there were good reasons to search for new anaesthetics. While my concern is with gaseous anaesthetics, I recognise that there were parallel developments in two related fields, that of topical or local anaesthetics, typified by the natural product cocaine and a host of synthetic substances, and injectable anaesthetics starting with opiates, then barbiturates and leading to modern materials such as propofol (2,6-diisopropylphenol). 2. Theories of anaesthetic action Hans Meyer1 noted that the anaesthetic substances were soluble in both fatty and aqueous media, proposed a general theory of anaesthesia based on the partition or distribution coefficient as a critical determinant. Meyer enunciated the following three principles that underpinned his theory: all chemically inert substances that are soluble in fats and fatty materials will produce narcosis; the line of action is in the nerve cells; the comparative strengths of substances depend on their solubility in fatty material and in water, that is, on the distribution coefficient. Charles Overton arrived at the same idea independently. Some years after completing his PhD research on cell permeability studies, Overton first presented his theory of narcosis in a lecture to the Society for Natural History in Zurich in October 1898, in a paper published the following year2 and in his book3 which included a full exposition.
  • Figure: 30 TAC §335.521(A)(2) [Figure: 30 TAC §335.521(A)(2)]

    Figure: 30 TAC §335.521(A)(2) [Figure: 30 TAC §335.521(A)(2)]

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  • (12) Patent Application Publication (10) Pub. No.: US 2007/0059270 A1 Hall Et Al

    (12) Patent Application Publication (10) Pub. No.: US 2007/0059270 A1 Hall Et Al

    US 2007005927OA1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2007/0059270 A1 Hall et al. (43) Pub. Date: Mar. 15, 2007 (54) ION EXCHANGE RESIN TREATED TO (22) Filed: Sep. 13, 2005 CONTROL, SWELLING Publication Classification (75) Inventors: Harlan Hall, Oregon, WI (US); J. Scott Madsen, Cottage Grove, WI (US) (51) Int. Cl. A 6LX 3L/795 (2006.01) Correspondence Address: (52) U.S. Cl. ............................................................ 424/78.1 CHALKER FLORES, LLP 2711 LBJ FRWY (57) ABSTRACT Suite 1036 DALLAS, TX 75234 (US) The present invention provides a method and composition are provided that includes an ion exchange resin treated with (73) Assignee: The Coating Place, Inc., Verona, WI from between about 0.01 to about 10 percent by weight of one or more Sugar alcohols in contact with one or more ionic (21) Appl. No.: 11/225,834 pharmaceutically active drug. US 2007/0059270 A1 Mar. 15, 2007 ON EXCHANGE RESIN TREATED TO CONTROL drug bound to an ion-exchange resin to provide a drug-resin SWELLING complex having a drug content above a specified value. The drug-resin complex is Subsequently coated with a water TECHNICAL FIELD OF THE INVENTION permeable diffusion barrier coating that is insoluble in 0001. The present invention relates general to the con gastrointestinal fluids. Thus, the release of drug is controlled trolled release of active agents, and in particular, to phar under conditions encountered in the gastrointestinal tract. macologically active drugs adsorbed to ion exchange resin. 0007 One of the major disadvantages with the use of an ion exchange resin as a pharmaceutical delivery agent is that BACKGROUND OF THE INVENTION ion exchange resin particles are Susceptible to Swelling.
  • The Hydrolysis of Phosphinates and Phosphonates: a Review

    The Hydrolysis of Phosphinates and Phosphonates: a Review

    molecules Review The Hydrolysis of Phosphinates and Phosphonates: A Review Nikoletta Harsági and György Keglevich * Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, 1521 Budapest, Hungary; [email protected] * Correspondence: [email protected]; Tel.: +36-1-463-1111 (ext. 5883) Abstract: Phosphinic and phosphonic acids are useful intermediates and biologically active com- pounds which may be prepared from their esters, phosphinates and phosphonates, respectively, by hydrolysis or dealkylation. The hydrolysis may take place both under acidic and basic conditions, but the C-O bond may also be cleaved by trimethylsilyl halides. The hydrolysis of P-esters is a challenging task because, in most cases, the optimized reaction conditions have not yet been explored. Despite the importance of the hydrolysis of P-esters, this field has not yet been fully surveyed. In order to fill this gap, examples of acidic and alkaline hydrolysis, as well as the dealkylation of phosphinates and phosphonates, are summarized in this review. Keywords: hydrolysis; dealkylation; phosphinates; phosphonates; P-acids 1. Introduction Phosphinic and phosphonic acids are of great importance due to their biological activity (Figure1)[ 1]. Most of them are known as antibacterial agents [2,3]. Multidrug- resistant (MDR) and extensively drug-resistant (XDR) pathogens may cause major problems Citation: Harsági, N.; Keglevich, G. in the treatment of bacterial infections. However, Fosfomycin has remained active against The Hydrolysis of Phosphinates and both Gram-positive and Gram-negative MDR and XDR bacteria [2]. Acyclic nucleoside Phosphonates: A Review. Molecules phosphonic derivatives like Cidofovir, Adefovir and Tenofovir play an important role 2021, 26, 2840.