Combined Prohibited and Restricted Chemical Lists
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Working with Hazardous Chemicals
A Publication of Reliable Methods for the Preparation of Organic Compounds Working with Hazardous Chemicals The procedures in Organic Syntheses are intended for use only by persons with proper training in experimental organic chemistry. All hazardous materials should be handled using the standard procedures for work with chemicals described in references such as "Prudent Practices in the Laboratory" (The National Academies Press, Washington, D.C., 2011; the full text can be accessed free of charge at http://www.nap.edu/catalog.php?record_id=12654). All chemical waste should be disposed of in accordance with local regulations. For general guidelines for the management of chemical waste, see Chapter 8 of Prudent Practices. In some articles in Organic Syntheses, chemical-specific hazards are highlighted in red “Caution Notes” within a procedure. It is important to recognize that the absence of a caution note does not imply that no significant hazards are associated with the chemicals involved in that procedure. Prior to performing a reaction, a thorough risk assessment should be carried out that includes a review of the potential hazards associated with each chemical and experimental operation on the scale that is planned for the procedure. Guidelines for carrying out a risk assessment and for analyzing the hazards associated with chemicals can be found in Chapter 4 of Prudent Practices. The procedures described in Organic Syntheses are provided as published and are conducted at one's own risk. Organic Syntheses, Inc., its Editors, and its Board of Directors do not warrant or guarantee the safety of individuals using these procedures and hereby disclaim any liability for any injuries or damages claimed to have resulted from or related in any way to the procedures herein. -
Transport of Dangerous Goods
ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions. -
Effect of Enzymes on Strawberry Volatiles During Storage, at Different Ripeness
Effect of Enzymes on Strawberry Volatiles During Storage, at Different Ripeness Level, in Different Cultivars and During Eating Thesis Presented in Partial Fulfillment of the Requirements for the Degree Master of Science in the Graduate School of The Ohio State University By Gulsah Ozcan Graduate Program in Food Science and Technology The Ohio State University 2010 Thesis Committee: Sheryl Ann Barringer, Adviser W. James Harper John Litchfield 1 Copyright by Gülşah Özcan 2010 ii ABSTRACT Strawberry samples with enzyme activity and without enzyme activity (stannous chloride added) were measured for real time formation of lipoxygenase (LOX) derived aroma compounds after 5 min pureeing using selected ion flow tube mass spectrometry (SIFT-MS). The concentration of (Z)-3-hexenal and (E)-2-hexenal increased immediately after blending and gradually decreased over time while hexanal concentration increased for at least 5 min in ground strawberries. The formation of hexanal was slower than the formation of (Z)-3-hexenal and (E)-2-hexenal in the headspace of pureed strawberries. The concentration of LOX aldehydes and esters significantly increased during refrigerated storage. Damaging strawberries increased the concentration of LOX aldehydes but did not significantly affect the concentration of esters. The concentrations of many of the esters were strongly correlated to their corresponded acids and/or aldehydes. The concentration of LOX generated aldehydes decreased during ripening, while fruity esters increased. Different varieties had different aroma profiles and esters were the greatest percentage of the volatiles. The aroma release of some of the LOX derived aldehydes in the mouthspace in whole strawberries compared to chopped strawberries showed that these volatiles are formed in the mouth during chewing. -
Coast Guard, DHS Pt. 150, App. I
Coast Guard, DHS Pt. 150, App. I APPENDIX I TO PART 150—EXCEPTIONS Member of reactive group Compatible with TO THE CHART Propylene glycol (20) (a) The binary combinations listed below Oleum (0) ............................... Hexane (31) have been tested as prescribed in Appendix Dichloromethane (36) III and found not to be dangerously reactive. Perchloroethylene (36) These combinations are exceptions to the 1,2-Propylene glycol (20) ...... Diethylenetriamine (7) Compatibility Chart (Figure 1) and may be Polyethylene polyamines (7) Triethylenetetramine (7) stowed in adjacent tanks. Sodium dichromate, 70% (0) Methyl alcohol (20) Member of reactive group Compatible with Sodium hydrosulfide solution Methyl alcohol (20) (5). Acetone (18) .......................... Diethylenetriamine (7) Iso-Propyl alcohol (20) Acetone cyanohydrin (0) ....... Acetic acid (4) Sulfuric acid (2) ..................... Coconut oil (34) Acrylonitrile (15) ..................... Triethanolamine (8) Coconut oil acid (34) Palm oil (34) 1,3-Butylene glycol (20) ......... Morpholine (7) Tallow (34) 1,4-Butylene glycol (20) ......... Ethylamine (7) Sulfuric acid, 98% or less (2) Choice white grease tallow Triethanolamine (8) (34) gamma-Butyrolactone (0) ...... N-Methyl-2-pyrrolidone (9) Caustic potash, 50% or less Isobutyl alcohol (20) (b) The binary combinations listed below (5). Ethyl alcohol (20) have been determined to be dangerously re- Ethylene glycol (20) active, based on either data obtained in the Isopropyl alcohol (20) Methyl alcohol (20) literature or on laboratory testing which has iso-Octyl alcohol (20) been carried out in accordance with proce- Caustic soda, 50% or less (5) Butyl alcohol (20) dures prescribed in Appendix III. These com- tert-Butyl alcohol, Methanol binations are exceptions to the Compat- mixtures ibility Chart (Figure 1) and may not be Decyl alcohol (20) stowed in adjacent tanks. -
Primary-Explosives
Improvised Primary Explosives © 1998 Dirk Goldmann No part of the added copyrighted parts (except brief passages that a reviewer may quote in a review) may be reproduced in any form unless the reproduced material includes the following two sentences: The copyrighted material may be reproduced without obtaining permission from anyone, provided: (1) all copyrighted material is reproduced full-scale. WARNING! Explosives are danegerous. In most countries it's forbidden to make them. Use your mind. You as an explosives expert should know that. 2 CONTENTS Primary Explosives ACETONE PEROXIDE 4 DDNP/DINOL 6 DOUBLE SALTS 7 HMTD 9 LEAD AZIDE 11 LEAD PICRATE 13 MEKAP 14 MERCURY FULMINATE 15 "MILK BOOSTER" 16 NITROMANNITE 17 SODIUM AZIDE 19 TACC 20 Exotic and Friction Primers LEAD NITROANILATE 22 NITROGEN SULFIDE 24 NITROSOGUANIDINE 25 TETRACENE 27 CHLORATE-FRICTION PRIMERS 28 CHLORATE-TRIMERCURY-ACETYLIDE 29 TRIHYDRAZINE-ZINC (II) NITRATE 29 Fun and Touch Explosives CHLORATE IMPACT EXPLOSIVES 31 COPPER ACETYLIDE 32 DIAMMINESILVER II CHLORATE 33 FULMINATING COPPER 33 FULMINATING GOLD 34 FULMINATING MERCURY 35 FULMINATING SILVER 35 NITROGEN TRICHLORIDE 36 NITROGEN TRIIODIDE 37 SILVER ACETYLIDE 38 SILVER FULMINATE 38 "YELLOW POWDER" 40 Latest Additions 41 End 3 PRIMARY EXPLOSIVES ACETONE PEROXIDE Synonyms: tricycloacetone peroxide, acetontriperoxide, peroxyacetone, acetone hydrogen explosive FORMULA: C9H18O6 VoD: 3570 m/s @ 0.92 g/cc. 5300 m/s @ 1.18 g/cc. EQUIVALENCE: 1 gram = No. 8 cap .75 g. = No. 6 cap SENSITIVITY: Very sensitive to friction, flame and shock; burns violently and can detonate even in small amounts when dry. DRAWBACKS: in 10 days at room temp. 50 % sublimates; it is best made immediately before use. -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Isoamyl Acetate
SUMMARY OF DATA FOR CHEMICAL SELECTION Isoamyl Acetate CAS No. 123-92-2 Prepared for NTP by Technical Resources International, Inc Prepared on 11/94 Under NCI Contract No. N01-CP-56019 Table of Contents I. Chemical Identification II. Exposure Information Table 1. Levels of isoamyl acetate reported in foods III. Evidence for Possible Carcinogenic Activity Appendix A: Structural Analogs of Isoamyl Acetate IV. References SUMMARY OF DATA FOR CHEMICAL SELECTION CHEMICAL IDENTIFICATION CAS Registry No.: 123-92-2 Chem. Abstr. Name: 1-Butanol, 3-methyl-, acetate Synonyms: Acetic acid 3-methylbutyl ester; acetic acid, isopentyl ester; AI3-00576; banana oil; isoamyl ethanoate; isopentyl acetate; isopentyl alcohol, acetate; pear oil; 3-methyl-1-butanol acetate; 3-methyl-1-butyl acetate; 3-methylbutyl acetate; 3-methylbutyl ethanoate; i-amyl acetate Structure: Molecular Formula and Molecular Weight: C7H14O2 Mol. Wt.: 130.18 Chemical and Physical Properties: Description: Colorless, flammable liquid with a banana-like odor (ACGIH, 1993). Boiling Point: 142°C (Lide, 1993) Melting Point: -78.5°C (Mark, et al, 1984; Lide, 1993) Solubility: Soluble in water (2000 mg/L at 25°C) (Howard, 1990); soluble in ethanol, diethyl ether, and acetone (Lide, 1993). Vapor 4.5 mm Hg at 20°C (Howard, 1990) Pressure: Refractive 1.4003 (Lide, 1993) Index: Flash Point: closed cup, 33°C; open cup, 38°:C (Budavari, 1989) Density: 0.876 (Lewis, 1993) Reactivity: Thermal decomposition of isoamyl acetate may produce acrid fumes. Contact with strong oxidizing agents, strong acids, and alkaline materials should be avoided (Haarmann & Reimer Corp., 1994). Hazardous decomposition products of isoamyl acetate include CO and CO2 (AESAR/Alfa, 1994) Log 2.13 (Howard, 1990) P(octanol/water partition coefficient): Technical Isoamyl acetate is commercially available as both a natural and synthetic product with a purity Products and range of 95-99+%. -
The List of Extremely Hazardous Substances)
APPENDIX A (THE LIST OF EXTREMELY HAZARDOUS SUBSTANCES) THRESHOLD REPORTABLE INVENTORY RELEASE QUANTITY QUANTITY CAS NUMBER CHEMICAL NAME (POUNDS) (POUNDS) 75-86-5 ACETONE CYANOHYDRIN 500 10 1752-30-3 ACETONE THIOSEMICARBAZIDE 500/500 1,000 107-02-8 ACROLEIN 500 1 79-06-1 ACRYLAMIDE 500/500 5,000 107-13-1 ACRYLONITRILE 500 100 814-68-6 ACRYLYL CHLORIDE 100 100 111-69-3 ADIPONITRILE 500 1,000 116-06-3 ALDICARB 100/500 1 309-00-2 ALDRIN 500/500 1 107-18-6 ALLYL ALCOHOL 500 100 107-11-9 ALLYLAMINE 500 500 20859-73-8 ALUMINUM PHOSPHIDE 500 100 54-62-6 AMINOPTERIN 500/500 500 78-53-5 AMITON 500 500 3734-97-2 AMITON OXALATE 100/500 100 7664-41-7 AMMONIA 500 100 300-62-9 AMPHETAMINE 500 1,000 62-53-3 ANILINE 500 5,000 88-05-1 ANILINE,2,4,6-TRIMETHYL- 500 500 7783-70-2 ANTIMONY PENTAFLUORIDE 500 500 1397-94-0 ANTIMYCIN A 500/500 1,000 86-88-4 ANTU 500/500 100 1303-28-2 ARSENIC PENTOXIDE 100/500 1 THRESHOLD REPORTABLE INVENTORY RELEASE QUANTITY QUANTITY CAS NUMBER CHEMICAL NAME (POUNDS) (POUNDS) 1327-53-3 ARSENOUS OXIDE 100/500 1 7784-34-1 ARSENOUS TRICHLORIDE 500 1 7784-42-1 ARSINE 100 100 2642-71-9 AZINPHOS-ETHYL 100/500 100 86-50-0 AZINPHOS-METHYL 10/500 1 98-87-3 BENZAL CHLORIDE 500 5,000 98-16-8 BENZENAMINE, 3-(TRIFLUOROMETHYL)- 500 500 100-14-1 BENZENE, 1-(CHLOROMETHYL)-4-NITRO- 500/500 500 98-05-5 BENZENEARSONIC ACID 10/500 10 3615-21-2 BENZIMIDAZOLE, 4,5-DICHLORO-2-(TRI- 500/500 500 FLUOROMETHYL)- 98-07-7 BENZOTRICHLORIDE 100 10 100-44-7 BENZYL CHLORIDE 500 100 140-29-4 BENZYL CYANIDE 500 500 15271-41-7 BICYCLO[2.2.1]HEPTANE-2-CARBONITRILE,5- -
Chem 353 Derivative Tables
ALCOHOLS Derivatives Mp/ oC Compound Bp /oC 3,5-Dinitro- Phenylurethane Naphthyl- (Mp / oC) benzoate urethane 4-Methylbenzyl alcohol --- (60) 118 79 --- Diphenylmethanol --- (69) 141 136 --- Ethyl p-hydroxybenzoate --- (116) * * * Methyl p-hydroxybenzoate --- (130) * * * Ethanol 78 93 52 79 2-Propanol 83 122 88 106 1-Propanol 97 74 51 80 2-Butanol 99 75 65 97 2-Methyl-1-propanol 108 86 86 104 3-Methyl-2-butanol 113 76 68 110 1-Butanol 116 64 63 71 3-Pentanol 116 101 48 95 2-Pentanol 119 61 --- (oil) 76 2-Chloroethanol 129 92 51 101 2-Methyl-1-butanol 129 70 31 82 3-Methyl-1-butanol 132 61 55 68 4-Methyl-2-pentanol 132 65 143 88 3-Methyl-2-pentanol 134 43 --- 72 1-Pentanol 138 46 46 68 2-Methyl-1-pentanol 148 51 --- 75 2-Ethyl-1-butanol 149 52 --- --- 1-Hexanol 156 58 42 59 Cyclohexanol 161 112 82 129 2-Octanol 179 32 114 63 1-Phenylethanol 203 95 94 106 Benzyl alcohol 205 112 78 134 2-Phenylethanol 219 108 79 119 Ethyl o-hydroxybenzoate 234 * * * Cinnamyl alcohol 257 (33) 121 90 114 4-Methoxybenzyl alcohol 260 (25) --- 92 --- * These compounds are also esters, see that table for derivatives. --- No data available. ESTERS Derivative Mp/ oC Compound Bp /oC Carboxylic (Mp / oC) Acid Methyl p-methylbenzoate 223 (30) 177 Methyl cinnamate 261 (35) 133 Methyl 4-methoxybenzoate 245 (49) 184 Ethyl p-nitrobenzoate --- (57) 241 Methyl p-nitrobenzoate --- (95) 241 Ethyl p-hydroxybenzoate --- (116) 213 Methyl p-hydroxybenzoate --- (130) 213 Methyl benzoate 198 121 Methyl o-toluate 213 102 Ethyl benzoate 213 121 Diethyl succinate 216 190 Methyl phenylacetate 218 76 Methyl salicylate 224 157 Methyl o-chlorobenzoate 230 140 Ethyl salicylate 234 157 Ethyl p-toluate 241 177 Isopropyl salicylate 255 157 Ethyl o-chlorobenzoate 255 140 Dimethyl suberate 268 141 Ethyl 4-methoxybenzoate 270 184 Ethyl cinnamate 271 133 Diethyl phthalate 296 230 --- No data available. -
Ch3ch2cch(Ch3)2 O Ch2ch2cho Ch3cch2ch2ch2cch2ch3
Chem 226 — Problem Set #9 — “Fundamentals of Organic Chemistry,” 4th edition, John McMurry. Chapter 9 2. Name the following aldehydes and ketones. O (a) (b) CH2CH2CHO CH3CH2CCH(CH3)2 H CH3 (c) O O (d) H C O CH3CCH2CH2CH2CCH2CH3 H (a) 2-methyl-3-pentanone, (b) 3-phenylpropanal, (c) 2,6-octanedione, (d) (1R,2R)-2-methylcyclohexanecarbaldehyde 4. How could you prepare pentanal from the following starting materials? (a) 1-pentanol, (b) CH3CH2CH2CH2COOH, (c) 5-decene PCC (a) CH3CH2CH2CH2CH2OH CH3CH2CH2CH2CHO CH2Cl2 O 1. LiAlH4 CH3CH2CH2CH2C OH CH3CH2CH2CH2CH2OH H O+ (b) 2. 3 PCC CH3CH2CH2CH2CH2OH CH3CH2CH2CH2CHO CH2Cl2 KMnO4 CH3CH2CH2CH2CH CHCH2CH2CH2CH3 + H3O O LiAlH (c) 1. 4 CH3CH2CH2CH2C OH + CH3CH2CH2CH2CH2OH 2. H3O PCC CH3CH2CH2CH2CH2OH CH3CH2CH2CH2CHO CH2Cl2 5. How could you prepare 2-hexanone from the following starting materials? (a) 2-hexanol, (b) 1-hexyne, (c) 2-methyl-1-hexene OH O K2CrO7 (a) CH3CH2CH2CH2CHCH3 CH3CH2CH2CH2CCH3 O H2SO4 (b) CH3CH2CH2CH2C CH CH3CH2CH2CH2CCH3 HgSO4 H2O CH3 O KMnO4 (c) CH3CH2CH2CH2C CH2 CH3CH2CH2CH2CCH3 + H3O (b) The enol that initially forms here undergoes keto-enol tautomerism. Terminal alkynes give methyl ketones; they follow Markovnikov’s rule. (c) Potassium permanganate under basic conditions would hydroxylate the alkene to form a vicinal diol, but under acidic conditions it completely cleaves the double bond. The =CH2 group would become carbon dioxide. 6. How would you carry out the following transformations? More than one step may be required. (a) 3-hexene 3-hexanone (b) benzene 1-phenylethanol H OH H2O (a) CH3CH2CH CHCH2CH3 CH3CH2CH CHCH2CH3 H SO 2 4 H O K2Cr2O7 CH3CH2CH CCH2CH3 O CH3CCl (b) C CH3 AlCl3 O H NaBH4 C CH3 OH 9. -
Tatp) Precursors and Synthetic By-Products
University of Central Florida STARS Electronic Theses and Dissertations, 2004-2019 2009 The Forensic Analysis Of Triacetone Triperoxide (tatp) Precursors And Synthetic By-products Kimberly Painter University of Central Florida Part of the Chemistry Commons, and the Forensic Science and Technology Commons Find similar works at: https://stars.library.ucf.edu/etd University of Central Florida Libraries http://library.ucf.edu This Masters Thesis (Open Access) is brought to you for free and open access by STARS. It has been accepted for inclusion in Electronic Theses and Dissertations, 2004-2019 by an authorized administrator of STARS. For more information, please contact [email protected]. STARS Citation Painter, Kimberly, "The Forensic Analysis Of Triacetone Triperoxide (tatp) Precursors And Synthetic By- products" (2009). Electronic Theses and Dissertations, 2004-2019. 4047. https://stars.library.ucf.edu/etd/4047 THE FORENSIC ANALYSIS OF TRIACETONE TRIPEROXIDE (TATP) PRECURSORS AND SYNTHETIC BY-PRODUCTS by KIMBERLY LYNNE PAINTER B.S. University of South Carolina, 2007 A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in the Department of Chemistry in the College of Sciences at the University of Central Florida Orlando, Florida Fall Term 2009 © 2009 Kimberly L. Painter ii ABSTRACT Triacetone Triperoxide (TATP) is a primary high explosive that can be synthesized using commercially available starting materials and has grown in use among terrorists over the past several years. Additives present in the precursors were investigated to see if they carry through the TATP synthesis and can be detected in the final product potentially aiding in the identification of the source. -
Each Lesson Section Is Divided Into Four Segmentsobjectives, a List of References, Suggested Activities, and ? Content Outline of the Material
DOCUMENT P7SUME ED 049 151 SP 007 022 AUTHOR Eeyer, Frederick Spooner, William Y. TITLE Earth Science. In-Seivice Television Program. INSTITUTION North Carolina State Board of Education, Raleigh. Dept.of Public Instruction. PUB DATE [70] NOTE 325p. EDRS PRICE EDRS Price MF-$0.65 HC-$13.16 DESCRIPTORS *Curriculum Guides, *Earth Science, Geoloyy, *Inservice Teacher Education, Meteorology, Oceanology, *Physical Geography, ',Se,,:ondary Education, Soil Science ABSTRACT GRADES OR AGES: Inservice course for secondary teacners. SUBJECT MATTER: Earth science. ORGANIZATION AND PHYSICAL APPEARANCE: The guide is intended for use with a 32- program television course f)c teachers, with material intended to be used in tne classroom. The introductory material explains the rationale of the course and includes the transmission schedule and bibliography. Each lesson section is divided into four segmentsobjectives, a list of references, suggested activities, and ? content outline of the material. The guide is offset printed and is in a looseleaf binder- OBJECTIVE:. AND ACTIVITIES: The o'cjectives are listed at the beginning of each lesson. Suggested activities arG included in each lesson and are intended to Provide examples of student investigation, demonstrations, or activities which will demonstrate 3 particular concept. INSTRUCTIONAL MATSFIALS: References to relevant printed material are given In each lesson, and other materials ate also referred to in the text. STUDENT ASSESSMENT: No provision is trade for evaluation. (MBM) US OF.TARTMENI OF HEALTH. EN/CA.710N & WE:JAME OFFICE OF EDUCATION THIS DOCLNIENT HAS BEEN REPRO- DUCED EXACTLY AS RECEIVED FROM THE PERSON OR ORGANIZATION OHIG :HATING IT POINTS OF VIEW OR 0.IN ,ONS STATED GO NOT NECESSARILY REPRESENT OFFICIAL OFF/CE OF EDU- CATION POSITION OR POLICY EARTH SCIENCE IN- SERVICE TELEVISION PROGRAM NORTH CAROLINA DEPARTMENT OF PUBLIC INSTRUCTION /RALEIGH PREPARED AND PRESENTED BY FREDERICK L.