Food and Drug Administration, HHS § 184.1138

Total Page:16

File Type:pdf, Size:1020Kb

Food and Drug Administration, HHS § 184.1138 Food and Drug Administration, HHS § 184.1138 (1) The ingredient is used as a dough (d) Prior sanctions for this ingredient strengthener as defined in § 170.3(o)(6) different from the uses established in of this chapter; a leavening agent as this section do not exist or have been defined in § 170.3(o)(17) of this chapter; waived. a pH control agent as defined in § 170.3(o)(23) of this chapter; and a [48 FR 52439, Nov. 18, 1983] texturizer as defined in § 170.3(o)(32) of § 184.1138 Ammonium chloride. this chapter. (2) The ingredient is used in food at (a) Ammonium chloride (NH4Cl, CAS levels not to exceed current good man- Reg. No. 12125–02–9) is produced by the ufacturing practice. reaction of sodium chloride and an am- (d) Prior sanctions for this ingredient monium salt in solution. The less solu- different from the uses established in ble sodium salt separates out at ele- this section do not exist or have been vated temperatures, and ammonium waived. chloride is recovered from the filtrate on cooling. Alternatively, hydrogen [48 FR 52439, Nov. 18, 1983] chloride formed by the burning of hy- § 184.1137 Ammonium carbonate. drogen in chlorine is dissolved in water and then reacted with gaseous ammo- (a) Ammonium carbonate ((NH4)2CO3, nia. Ammonium chloride is crystallized CAS Reg. No. 8000–73–5) is a mixture of from the solution. ammonium bicarbonate (NH4HCO3) and (b) The ingredient meets the speci- ammonium carbamate (NH2COONH4). fications of the Food Chemicals Codex, It is prepared by the sublimation of a 3d Ed. (1981), p. 20, which is incor- mixture of ammonium sulfate and cal- porated by reference. Copies are avail- cium carbonate and occurs as a white able from the National Academy Press, powder or a hard, white or translucent 2101 Constitution Ave, NW., Wash- mass. ington, DC 20418, or available for in- (b) The ingredient meets the speci- spection at the National Archives and fications of the Food Chemicals Codex, Records Administration (NARA). For 3d Ed. (1981), p. 19, which is incor- information on the availability of this porated by reference. Copies are avail- material at NARA, call 202–741–6030, or able from the National Academy Press, go to: http://www.archives.gov/ 2101 Constitution Ave. NW., Wash- ington, DC 20418, or available for in- federallregister/ spection at the National Archives and codeloflfederallregulations/ Records Administration (NARA). For ibrllocations.html. information on the availability of this (c) In accordance with § 184.1(b)(1), material at NARA, call 202–741–6030, or the ingredient is used in food with no go to: http://www.archives.gov/ limitation other than current good federallregister/ manufacturing practice. The affirma- codeloflfederallregulations/ tion of this ingredient as generally rec- ibrllocations.html. ognized as safe (GRAS) as a direct (c) In accordance with § 184.1(b)(1), human food ingredient is based upon the ingredient is used in food with no the following current good manufac- limitation other than current good turing practice conditions of use: manufacturing practice. The affirma- (1) The ingredient is used as a dough tion of this ingredient as generally rec- strengthener as defined in § 170.3(o)(6) ognized as safe (GRAS) as a direct of this chapter; a flavor enhancer as de- human food ingredient is based upon fined in § 170.3(o)(11) of this chapter; a the following current good manufac- leavening agent as defined in turing practice conditions of use: § 170.3(o)(17) of this chapter; and a proc- (1) The ingredient is used as a leav- essing aid as defined in § 107.3(o)(24) of ening agent as defined in § 170.3(o)(17) of this chapter. this chapter and a pH control agent as (2) The ingredient is used in food at defined in § 170.3(o)(23) of this chapter. levels not to exceed current good man- (2) The ingredient is used in food at ufacturing practice. levels not to exceed current good man- (d) Prior sanctions for this ingredient ufacturing practice. different from the uses established in 503 VerDate Sep<11>2014 08:58 Jul 06, 2015 Jkt 235072 PO 00000 Frm 00513 Fmt 8010 Sfmt 8010 Y:\SGML\235072.XXX 235072 Lhorne on DSK7TPTVN1PROD with CFR.
Recommended publications
  • A Study on Physical Chemistry of Solid a Mmonium Materials for Nox Reduction of Diesel Engine Emissions
    A Study on Physical Chemistry of Solid A mmonium Materials for NOx Reduction of Diesel Engine Emissions Cheon Seog (Steve) Yoon and Jong Kook Shin Hannam University, Daejeon, KOREA Hoyeol Lee and Hongsuk Kim Korea Institute of Machinery & Materials, Daejeon, KOREA 2014 DOE CLEERS Workshop University of Michigan, Dearborn, MI, USA 1 Table of Contents • Introduction of Solid SCR System • Ammonium Salts • Chemical Reactions, Decomposition Chemistry • Chemical Kinetic Parameters by TGA, DTA and DSC • Decomposition Rate from Hot Plate Test and Chemical Kinetic Parameters • Simple Reactor with Visible Window • Equilibrium Vapor Pressure Curve for Ammonium Carbonate • Acquisition of Re-solidified Materials from Ammonium Carbonate • Analytical Study of Re-solidified Materials from Ammonium Carbonate by XRD, FT-IR, and EA • Concluding Remarks • Acknowledgement • Reference 2 Solid SCR System • NOx purification technology by using NH3, which is generated from solid ammonium. • Ammonium carbonate, (NH4)2CO3 , is solid at room temperature, and it decomposes into NH3, H2O & CO2 above temperature of 60℃. 3 Material Properties of Ammonium Salts Solid urea Ammonium carbonate Ammonium cabarmate Molecular formula (NH2)2CO (NH4)2CO3 NH2COONH4 Molecular weight 60.07 96.09 78.07 3 Density, g/cm 1.33 1.5 1.6 Mols NH3 per Mol 2 2 2 Mols NH3 per kg 33.3 20.8 25.6 Decomposition temp., ℃ 140 58 60 NH2CONH2↔ NH3+HNCO Reaction mechanism (NH4)2CO3↔2NH3+CO2+H2O NH4COONH2 ↔ 2NH3 + CO2 HNCO +H2O ↔ NH3 + CO2 Cost cheap cheap moderate * HNCO: Isocyanic Acid [ref] G. Fulks,
    [Show full text]
  • 1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
    1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5-
    [Show full text]
  • Environmental Protection Agency § 117.3
    Environmental Protection Agency § 117.3 (4) Applicability date. This paragraph TABLE 117.3—REPORTABLE QUANTITIES OF (i) is applicable beginning on February HAZARDOUS SUBSTANCES DESIGNATED PUR- 6, 2020. SUANT TO SECTION 311 OF THE CLEAN (j) Process waste water means any WATER ACT—Continued water which, during manufacturing or Cat- RQ in pounds processing, comes into direct contact Material egory (kilograms) with or results from the production or use of any raw material, intermediate Ammonium benzoate ...................... D ...... 5,000 (2,270) Ammonium bicarbonate .................. D ...... 5,000 (2,270) product, finished product, byproduct, Ammonium bichromate ................... A ....... 10 (4.54) or waste product. Ammonium bifluoride ...................... B ....... 100 (45.4) Ammonium bisulfite ......................... D ...... 5,000 (2,270) [44 FR 50776, Aug. 29, 1979, as amended at 58 Ammonium carbamate .................... D ...... 5,000 (2,270) FR 45039, Aug. 25, 1993; 65 FR 30904, May 15, Ammonium carbonate ..................... D ...... 5,000 (2,270) 2000; 80 FR 37112, June 29, 2015; 83 FR 5208, Ammonium chloride ........................ D ...... 5,000 (2,270) Feb. 6, 2018] Ammonium chromate ...................... A ....... 10 (4.54) Ammonium citrate dibasic ............... D ...... 5,000 (2,270) Ammonium fluoborate ..................... D ...... 5,000 (2,270) § 117.2 Abbreviations. Ammonium fluoride ......................... B ....... 100 (45.4) NPDES equals National Pollutant Ammonium hydroxide ..................... C
    [Show full text]
  • United States Patent (19) 11 Patent Number: 5,788,915 Blount (45) Date of Patent: Aug
    IIIUSOO5788915A United States Patent (19) 11 Patent Number: 5,788,915 Blount (45) Date of Patent: Aug. 4, 1998 54 FLAME RETARDANT COMPOSITIONS 57 ABSTRACT UTILIZING PARTIALLY HYDROLYZED AMNO CONDENSATON COMPOUNDS Flame retardant compositions of this invention are produced by incorporating a partially index (LOI) hydrolyzed amino 76 Inventor: David H. Blount, 6728 Del Cerro condensation composition in a more flammable organic Blvd., San Diego, Calif. 92120 material. The partially hydrolyzed amino condensation com pounds are produced by heating urea or heating urea with (21) Appl. No.: 801,776 other nitrogen containing compounds that will condensate with or react with isocyanic acid and/or cyanic acid thereby 22 Filed: Feb. 14, 1997 producing an amino condensation compound which is then Related U.S. Application Data partially hydrolysis is done by reacting it with a limited amount of water. The partially hydrolyzed amino conden 62) Division of Ser. No. 723,779, Sep. 30, 1996. sation compounds may be used alone or may be mixed with or reacted with carbonization auxiliaries, aldehydes and (51) Int. Cl. ........................ C09K 21A00; C08G 12/12 fillers to produce a partially hydrolyzed amino condensation 52 U.S. Cl. ........................... 252/609; 528/259; 252/601 composition which is incorporated in more flammable 58) Field of Search ..................................... 252/609, 601: organic compositions such as polyurethanes, polyester 528/259 resins. epoxy resins, vinyl resins and other resins. The partially hydrolyzed amino condensation salts of 56 References Cited phosphorus, boron or sulfur containing compounds and the U.S. PATENT DOCUMENTS partially hydrolyzed amino condensation-aldehyde resins 3,900,665 8/1975 Weil .......................................
    [Show full text]
  • Ammonium Carbonate. Drogen in Chlorine Is Dissolved in Water and Then Reacted with Gaseous Ammo- (A) Ammonium Carbonate ((NH4)2CO3, Nia
    Food and Drug Administration, HHS § 184.1138 (1) The ingredient is used as a dough (d) Prior sanctions for this ingredient strengthener as defined in § 170.3(o)(6) different from the uses established in of this chapter; a leavening agent as this section do not exist or have been defined in § 170.3(o)(17) of this chapter; waived. a pH control agent as defined in § 170.3(o)(23) of this chapter; and a [48 FR 52439, Nov. 18, 1983] texturizer as defined in § 170.3(o)(32) of § 184.1138 Ammonium chloride. this chapter. (2) The ingredient is used in food at (a) Ammonium chloride (NH4Cl, CAS levels not to exceed current good man- Reg. No. 12125–02–9) is produced by the ufacturing practice. reaction of sodium chloride and an am- (d) Prior sanctions for this ingredient monium salt in solution. The less solu- different from the uses established in ble sodium salt separates out at ele- this section do not exist or have been vated temperatures, and ammonium waived. chloride is recovered from the filtrate on cooling. Alternatively, hydrogen [48 FR 52439, Nov. 18, 1983] chloride formed by the burning of hy- § 184.1137 Ammonium carbonate. drogen in chlorine is dissolved in water and then reacted with gaseous ammo- (a) Ammonium carbonate ((NH4)2CO3, nia. Ammonium chloride is crystallized CAS Reg. No. 8000–73–5) is a mixture of from the solution. ammonium bicarbonate (NH4HCO3) and (b) The ingredient meets the speci- ammonium carbamate (NH2COONH4). fications of the Food Chemicals Codex, It is prepared by the sublimation of a 3d Ed.
    [Show full text]
  • E60 Sodium Lauryl Sulfate 3 Revision Stage 2 4 5 Definition
    003-1903PDG.pdf 1 2 E60 Sodium Lauryl Sulfate 3 Revision Stage 2 4 5 Definition 6 Sulfuric acid monododecyl ester sodium salt. 7 Sodium monododecyl sulfate [151-21-3]. 8 Sodium Lauryl Sulfate is a mixture of sodium alkyl sulfates consisting chiefly of sodium lauryl 9 sulfate [CH3(CH2)10CH2OSO3Na]. It contains not less than 85.0% of sodium alkyl sulfates 10 calculated as C12H25NaO4S. 11 12 Identification 13 A: Infrared absorption spectrophotometry – KBr or ATR 14 Record the infrared absorption spectrum of Sodium Lauryl Sulfate and compare with the 15 spectrum obtained with the Reference Standard: the transmission minima correspond in 16 position and relative size. 17 18 B: Place 2.5 g in a silica or platinum crucible, and add 2 mL of 10 N sulfuric acid. Heat on a water 19 bath, then cautiously raise the temperature progressively over an open flame. Ignite, preferably in 20 a muffle furnace, at 600 ± 25 . Continue heating until all black particles have disappeared. Cool, 21 add a few drops of 2 N sulfuric acid, and heat and ignite as above. Add a few drops of ammonium 22 carbonate solution, evaporate to dryness, and ignite as above. Cool, dissolve the residue in 50 mL 23 of water, and mix. 24 To a 2 mL portion of this solution, add 4 mL of Potassium pyroantimonate solution. If necessary, 25 rub the inside of the test tube with a glass rod. A white, crystalline precipitate is formed. 26 27 C: Prepare a solution (1 in 10) after acidification with hydrochloric acid and boiling for 20 minutes.
    [Show full text]
  • Ammonium Carbamate Acm
    AMMONIUM CARBAMATE ACM CAUTIONARY RESPONSE INFORMATION 4. FIRE HAZARDS 7. SHIPPING INFORMATION 4.1 Flash Point: 7.1 Grades of Purity: Currently not available Common Synonyms Solid crystalline White Ammonia odor Not flammable 7.2 Storage Temperature: Cool Ammonium aminoformate powder 4.2 Flammable Limits in Air: Currently not 7.3 Inert Atmosphere: Currently not available Anhydride of ammonium available carbonate 7.4 Venting: Currently not available Carbamic acid, ammonium salt Mixes with water. 4.3 Fire Extinguishing Agents: Carbon dioxide, dry chemical, or water spray 7.5 IMO Pollution Category: Currently not available 4.4 Fire Extinguishing Agents Not to Be 7.6 Ship Type: Currently not available Wear goggles, self-contained breathing apparatus, and rubber gloves. Keep people away. Used: Currently not available Stop discharge if possible. Call fire department. 7.7 Barge Hull Type: Currently not available Isolate and remove discharged material. 4.5 Special Hazards of Combustion Products: Currently not available Notify local health and pollution control agencies. 8. HAZARD CLASSIFICATIONS Protect water intakes. 4.6 Behavior in Fire: Moderate fire and explosion hazards when exposed to heat 8.1 49 CFR Category: Not listed Fire COMBUSTIBLE. or flame 8.2 49 CFR Class: Not pertinent POISONOUS GAS MAY BE PRODUCED IN FIRE OR WHEN HEATED. 4.7 Auto Ignition Temperature: Not pertinent 8.3 49 CFR Package Group: Not listed. Wear self-contained breathing apparatus, goggles, rubber gloves, and normal 4.8 Electrical Hazards: Not pertinent protective gear. 8.4 Marine Pollutant: No 4.9 Burning Rate: Not pertinent Extinguish with CO2 dry chemical, or water spray.
    [Show full text]
  • PRODUCTION of UREA and UREA AMMONIUM NITRATE
    Best Available Techniques for Pollution Prevention and Control in the European Fertilizer Industry Booklet No. 5 of 8: PRODUCTION OF UREA and UREA AMMONIUM NITRATE 2000 EFMA European Fertilizer Manufacturers’ Association Ave. E van Nieuwenhuyse 4 B-1160 Brussels Belgium Best Available Techniques for Pollution Prevention and Control in the European Fertilizer Industry Booklet No. 5 of 8: PRODUCTION OF UREA and UREA AMMONIUM NITRATE Copyright 2000 – EFMA This publication has been prepared by member companies of the European Fertilizer Manufacturers’ Association (EFMA). Neither the Association nor any individual member company can accept liability for accident or loss attributable to the use of the information given in this Booklet. Booklet No. 1 No. 5 Hydrocarbon feed Urea Water Ammonia Air UAN No. 2 No. 6 Water AN Nitric Acid Air Calcium carbonate CAN No. 3 No. 7 Water NPK Sulphuric Acid Phosphate rock (nitrophosphate Sulphur route) K, Mg, S, micronutrients No. 4 No. 8 NPK Water Phosphoric (mixed acid Phosphate Acid route) rock K, Mg, S, micronutrients Phosphate rock 2 CONTENTS PREFACE 5 DEFINITIONS 7 1. INTRODUCTION 8 2. DESCRIPTION OF UREA PRODUCTION PROCESSES 8 2.1 Urea Plant Installations in Europe 12 2.2 Description of BAT Production Processes 12 2.3 Process Water Sources and Quantities 13 2.4 Prilling and Granulation 14 2.5 Feasible and Available Emission Abatement Techniques 16 2.6 Description of Process Water BAT Treatment Systems 16 2.7 Prill Tower Emissions 18 2.8 Granulator Emissions 20 3. DESCRIPTION OF STORAGE AND TRANSFER EQUIPMENT 20 3.1 Ammonia 20 3.2 Carbon Dioxide 21 3.3 Formaldehyde 21 4.
    [Show full text]
  • Ammonium Carbamate Hazard Summary Identification
    Common Name: AMMONIUM CARBAMATE CAS Number: 1111-78-0 RTK Substance number: 0091 DOT Number: NA 9083 Date: January 1996 Revision: March 2002 ------------------------------------------------------------------------- ------------------------------------------------------------------------- HAZARD SUMMARY WORKPLACE EXPOSURE LIMITS * Ammonium Carbamate can affect you when breathed in. The following exposure limits are for Ammonia: * Exposure can irritate the skin and eyes causing redness and tearing. OSHA: The legal airborne permissible exposure limit * Breathing Ammonium Carbamate can irritate the nose, (PEL) is 50 ppm averaged over an 8-hour throat and lungs causing coughing and/or shortness of workshift. breath. NIOSH: The recommended airborne exposure limit is IDENTIFICATION 25 ppm averaged over a 10-hour workshift and Ammonium Carbamate is a white crystalline (sand-like) 35 ppm, not to be exceeded during any 15 minute powder. It is used as a fertilizer and ammoniating agent. work period. REASON FOR CITATION ACGIH: The recommended airborne exposure limit is 25 ppm averaged over an 8-hour workshift and * Ammonium Carbamate is on the Hazardous Substance 35 ppm as a STEL (short-term exposure limit). List because it is cited by DOT and EPA. * Definitions are provided on page 5. WAYS OF REDUCING EXPOSURE HOW TO DETERMINE IF YOU ARE BEING * Where possible, enclose operations and use local exhaust ventilation at the site of chemical release. If local exhaust EXPOSED ventilation or enclosure is not used, respirators should be The New Jersey Right to Know Act requires most employers worn. to label chemicals in the workplace and requires public * Wear protective work clothing. employers to provide their employees with information and * Wash thoroughly immediately after exposure to training concerning chemical hazards and controls.
    [Show full text]
  • Problem Set - Balancing Chemical Equations I
    Problem Set - Balancing Chemical Equations I Name: Chemistry Period: Date: RF Mandes, PhD, NBCT Part I Balance each chemical equation by placing the appropriate coefficient in the blank. Write the Reaction Type on the blank. 1. _2_LiBr + _1_ K2SO4 2__KBr + _1_Li2SO4 double replacement 2. _1_PBr3 + _3_NaOH _1_P(OH)3 + _3_NaBr double replacement 3. _1_Ca(NO3)2 _1_ Ca(NO2)2 + _1_O2 decomposition 4. _2_Fe + _3_H2SO4 _1_Fe2(SO4)3 + _3_H2 single replacement 5. _4_H2S + _2_CS2 _2_CH4 + _1_S8 N/A 6. __1 N2 + _3_Mg _1_Mg3N2 single replacement 7. _16_NiO + 1__S8 _16_Ni + _8_SO2 single replacement 8. _3_Pt + _2_Ni2(SO3)3 _3_Pt(SO3)2 + _4_Ni single replacement 9. _2_H2O2 _2_H2O + _1_O2 decomposition 10. _1_SrC2 + _2_H2O _1_Sr(OH)2 + _2_C2H2 N/A 11. _1_OsO4 + _4_H2 _1_Os + _4_H2O single replacement 12 . _2_IrCl3 + _3_NaOH _1_Ir2O3 + _3_HCl + _3_NaCl Problem Set - Balancing Chemical Equations I Part II Convert the word equation into a chemical equation by writing the formula of each compound. Then balance the chemical equation. 13. iron + oxygen iron (III) oxide Equation: Fe + O2 Fe2O3 14. zinc + sodium chloride zinc (II) chloride + sodium Equation: Zn NaCl ZnCl2 + Na 15. calcium nitrate + lithium sulfate calcium sulfate + lithium nitrate Equation: Ca(NO3)2 + Li2SO4 CaSO4 + LiNO3 Part III Write the word equation that corresponds to the reaction that is described. Then convert the word equation into an unbalanced chemical equation 16. When calcium carbonate is heated strongly, carbon dioxide gas is driven off, leaving a residue of calcium oxide in the flask. Word equation: calcium carbonate → carbon dioxide + calcium oxide Unbalanced equation: CaCO3 → CO2 + CaO 17. Solid ammonium carbonate, (NH4)2CO3, is used as the active ingredient in smelling salts.
    [Show full text]
  • Orca Corrosion Chart
    Unsaturated Polyester Vinylster (Epoxy Acrylate Resins) CHEMICAL Conc Resins NO ISO BIS Novolac Bromine ENVIRONMENT % 511/512 301 585 570 545/555 A 1 Acetaldehyde 20 NR 40 40 40 2 Acetic Acid 10 80 100 100 100 3 Acetic Acid 15 60 100 100 100 4 Acetic Acid 25 60 100 100 100 5 Acetic Acid 50 - 80 80 80 6 Acetic Acid 75 NR 65 65 65 7 Acetic Acid, Glacial 100 NR NR 40 NR 8 Acetic Anhydride 100 NR NR 40 NR 9 Acetone 10 NR NR 80 80 10 Acetone 100 NR NR NR NR 11 Acetonitrile 20 - 40 40 40 12 Acetyl Acetone 20 - 40 50 40 13 Acrolein (Acrylaldehyde) 20 - 40 40 40 14 Acrylamide 50 NR 40 40 40 15 Acrylic Acid 25 NR 40 40 40 16 Acrylic Latex All - 80 80 80 17 Acrylonitrile Latex Dispersion 2 NR 25 25 25 Activated Carbon Beds, Water 18 - 80 100 80 Treatment Adipic Acid(1.5g solution in 19 23 - 80 80 80 water at 25℃, sol in hot water) 20 ALAMINE amines - 65 80 65 21 Alkyl(C8-10) Dimethyl Amine 100 - 80 100 80 22 Alkyl(C8-10) Chloride All - 80 100 95 23 Alkyl Benzene Sulfonic Acid 90 NR 50 50 50 Alkyl Tolyl Trimethyl 24 - - 40 50 40 Ammonium Chloride 25 Allyl Alcohol 100 NR NR 25 NR 26 Allyl Chloride All NR 25 25 25 27 Alpha Methylstyrene 100 NR 25 50 25 28 Alpha Oleum Sulfates 100 NR 50 50 50 29 Alum Sat'd 80 100 120 100 30 Aluminum Chloride Sat'd 80 100 120 100 31 Aluminum Chlorohydrate All - 100 100 100 32 Aluminum Chlorohydroxide 50 - 100 100 100 33 Aluminum Fluoride All - 25 25 25 34 Aluminum Hydroxide 100 80 80 95 80 35 Aluminum Nitrate All 80 100 100 100 36 Aluminum Potassium Sulfate Sat'd 80 100 120 100 37 Aluminum Sulfate Sat'd 80 100 120 100
    [Show full text]
  • List of Lists
    United States Office of Solid Waste EPA 550-B-10-001 Environmental Protection and Emergency Response May 2010 Agency www.epa.gov/emergencies LIST OF LISTS Consolidated List of Chemicals Subject to the Emergency Planning and Community Right- To-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act • EPCRA Section 302 Extremely Hazardous Substances • CERCLA Hazardous Substances • EPCRA Section 313 Toxic Chemicals • CAA 112(r) Regulated Chemicals For Accidental Release Prevention Office of Emergency Management This page intentionally left blank. TABLE OF CONTENTS Page Introduction................................................................................................................................................ i List of Lists – Conslidated List of Chemicals (by CAS #) Subject to the Emergency Planning and Community Right-to-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act ................................................. 1 Appendix A: Alphabetical Listing of Consolidated List ..................................................................... A-1 Appendix B: Radionuclides Listed Under CERCLA .......................................................................... B-1 Appendix C: RCRA Waste Streams and Unlisted Hazardous Wastes................................................ C-1 This page intentionally left blank. LIST OF LISTS Consolidated List of Chemicals
    [Show full text]