File Hazchem.jpg thumb right 250px A sample Hazchem plate Hazchem is a warning plate system used in Australia , Malaysia , New Zealand and the United Kingdom for vehicles transporting dangerous goods hazardous substances , and on storage facilities housing such substances. Part of the Hazchem plate carries information on how an emergency service should deal with an incident pertaining to the vehicle or facility. Hazchem is not the ADR Hazard Identification Number HIN , also known as the Kemler Code , as this is a different warning plate carried by vehicles in the rest of the EU. The main difference is the HIN details the nature of the hazard presented by the goods as opposed to the actions to be taken when dealing with them. The top left section of the plate gives the Emergency Action Code EAC telling the fire brigade what actions to take if there s an accident. The middle left section gives ... logo the flower is a sample logo . There is also a standard null Hazchem plate to indicate the transport .... The National Chemical Emergency Centre in the United Kingdom provides a Free Online Hazchem Guide. ref http www.the ncec.com hazchem Free Online Hazchem Guide ref Emergency Action Code The Emergency ... Government CLG to edit the EAC List 2007 publication, outlining the application of Hazchem Emergency ... 2009 HazChem fire suppression class wikitable border 1 float right Number Action 1 Jets 2 Fog sup ... of the other methods use water. HazChem safety parameters Each EAC contains at least one letter .... File Nswrfsfpbhazchem.jpg 500px right HazChem information within the NSW Rural Fire Service Firefighters ... System References references External links http www.the ncec.com hazchemHazchem Guide ... codes list 2009 Download EAC List 2009 http www.hazchem.freeuk.com panel.htm Example of UK Hazchem Panel with Hazchem Emergency Action Code EAC http www.hazchem.freeuk.com index.htm General Hazchem ... HAZCHEM Emergency Action Code ... more details
Unreferenced date December 2011 Chembox Name Dimethylamidophosphoric dichloride ImageFile1 Dimethylamidophosphoric dichloride 3D balls by AHRLS.png ImageName1 Dimethyl amidophosphoric dichloride 3D balls ImageSize1 200px ImageFile2 Dimethylamidophosphoric dichloride 2D skeletal by AHRLS 2011.png ImageName2 Dimethylamidophosphoric dichloride 2D skeletal ImageSize2 200px OtherNames Dimethylamido phosphoryl dichloride N , N Dimethylphosphoramidodichloridate IUPACName N Dichlorophosphoryl N methylmethanamine Section1 Chembox Identifiers CASNo PubChem 12673 SMILES CN C P O Cl Cl InChI 1S C2H6Cl2NOP c1 5 2 7 3,4 6 h1 2H3 InChIKey YNHXBEVSSILHPI UHFFFAOYSA N Section2 Chembox Properties C 2 H 6 O 1 P 1 Cl 2 MeltingPt 0 C Section7 Chembox Hazards EUClass Hazchem C Hazchem N Hazchem T EUIndex NFPA H 3 NFPA F 3 NFPA R 2 NFPA O W Dimethylamidophosphoric dichloride is an important chemical for few industrial purposes. It is an important chemical for synthesizing phosphoramidate s as well as Tabun nerve agent Nerve agent GA which is used as a chemical weapon. Safety This chemical is also corrosive, flammable and will cause mild nerve agent symptoms if ingested or absorbed through skin due to its nature. It will react with water giving off hydrogen chloride vapors and dimethylamidophosphoric acid . See also Organophosphate poisoning Category Organophosphates fa ... more details
wiktionary hazmat Hazmat , HazMat and similar terms can refer to Hazardous materials and items see Dangerous goods Hazchem a system of hazardous chemical classification and firefighting modes A hazmat suit is a type of protective clothing Hazmat comics is a Marvel Comics Electronic Arts character Hazmat Modine , a blues indie folk world fusion musical group from New York disambig ... more details
Unreferenced date December 2011 chembox verifiedrevid 474952423 Name Dimethylamidophosphoric dicyanide ImageFile1 Dimethylamidophosphoric dicyanide 3D balls by AHRLS 2011.png ImageName1 Dimethylamidophosphoric dicyanide 3D model ImageSize1 200px ImageFile2 Dimethylamidophosphoric dicyanide 2D skeletal by AHRLS.png ImageName2 Dimethylamidophosphoric dicyanide 2D structure ImageSize2 200px OtherNames Dimethylamido phosphoryl dicyanide N , N Dimethylphosphoramidodicyanidate IUPACName N Dicyanophosphoryl N methylmethanamine Section1 Chembox Identifiers CASNo Ref cascite correct ?? CASNo PubChem 12673 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 26327732 SMILES CN C P O C N C N InChI 1 C4H6N3OP c1 7 2 9 8,3 5 4 6 h1 2H3 InChIKey REFCDSGCMMWWTR UHFFFAOYAK StdInChI Ref stdinchicite correct chemspider StdInChI 1S C4H6N3OP c1 7 2 9 8,3 5 4 6 h1 2H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey REFCDSGCMMWWTR UHFFFAOYSA N Section2 Chembox Properties C 4 H 6 O 1 P 1 N 3 Section7 Chembox Hazards EUClass Hazchem C Hazchem N Hazchem T Hazchem F EUIndex NFPA H 4 NFPA F 3 NFPA R 2 NFPA O W RPhrases R26 27 28 , R15 29 RSPhrases SPhrases S1 2 , S3 7 , S36 37 39 , S23 , S28 , S38 , S45 Dimethylamidophosphoric dicyanide is an important chemical for the final process of synthesizing Tabun nerve agent Tabun , a nerve agent used as a chemical weapon. Preparation Dimethylamidophosphoric dicyanide could be prepared by reacting Dimethylamidophosphoric dichloride with sodium cyanide . Image Synthesis of Dimethylamidophosphoric dicyanide 2D by AHRLS.png 500px Safety This chemical is very flammable, highly toxic and reactive. If ingested or absorbed through skin, it will cause mild nerve agent symptoms directly as well as blood agent symptoms due to release of hydrogen cyanide HCN . In contact with water also will gives off poisonous hydrogen cyanide fumes and dimethylamidophosphoric acid . See also Organophosphate poisoning hydrogen cyanide Category Organophosp ... more details
chembox verifiedrevid 401926786 ImageFile Benzyl chloroformate 2D skeletal.png ImageName Skeletal formula of benzyl chloroformate ImageFile1 Benzyl chloroformate 3D balls.png ImageName1 Ball and stick model of the benzyl chloroformate molecule IUPACName Benzyloxycarbonyl chloride br Benzyl chloroformate Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 9958 InChI 1 C8H7ClO2 c9 8 10 11 6 7 4 2 1 3 5 7 h1 5H,6H2 InChIKey HSDAJNMJOMSNEV UHFFFAOYAW StdInChI Ref stdinchicite correct chemspider StdInChI 1S C8H7ClO2 c9 8 10 11 6 7 4 2 1 3 5 7 h1 5H,6H2 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey HSDAJNMJOMSNEV UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 501 53 1 PubChem 10387 SMILES ClC O OCc1ccccc1 Section2 Chembox Properties C 8 H 7 Cl 1 O 2 Density 1.195 g cm sup 3 sup MeltingPt 0 C BoilingPt 103 C 20 Torr Section7 Chembox Hazards EUClass Hazchem C Hazchem N Hazchem Xn ExternalMSDS http msds.chem.ox.ac.uk BE benzyl chloroformate.html External MSDS EUIndex 607 064 00 4 RPhrases R34 , R50 53 SPhrases S1 2 , S26 , S45 , S60 , S61 FlashPt 80 C Benzyl chloroformate is the benzyl ester of chloroformic acid . It is also known as benzyl chlorocarbonate and is an oily liquid whose color is anywhere from yellow to colorless. It is also known for its pungent odor. When heated, benzyl chloroformate decomposes into phosgene and if it comes in contact with water it produces toxic, corrosive fumes. Benzyl chloroformate is used in organic synthesis for the introduction of the carboxybenzyl Cbz or Z protecting group for amine s File Cbz.PNG 450px The newly formed Cbz protecting group can be removed under reductive conditions. Typically hydrogen gas and activated palladium on carbon is used. External links ICSC 0990 09 Category Chloroformates Category Reagents for organic chemistry ester stub de Chlorameisens urebenzylester fr Chloroformiate de benzyle id Benzil kloroformat nl Benzylchloorformiaat ja ... more details
chembox Reference ref http www.sigmaaldrich.com catalog ProductDetail.do?N4 23211 FLUKA&N5 SEARCH CONCAT PNO BRAND KEY&F SPEC Methyl chloroformate at Sigma Aldrich ref verifiedrevid 472248678 ImageFile Methyl chloroformate.png ImageName Skeletal formula of methyl chloroformate ImageFile1 Methyl chloroformate 3D balls.png ImageName1 Ball and stick model of the methyl chloroformate molecule IUPACName methyl carbonochloridate Section1 Chembox Identifiers CASNo Ref cascite correct CAS CASNo 79 22 1 PubChem 6586 SMILES O C Cl OC ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 6337 SMILES ClC O OC InChI 1 C2H3ClO2 c1 5 2 3 4 h1H3 InChIKey XMJHPCRAQCTCFT UHFFFAOYAT StdInChI Ref stdinchicite correct chemspider StdInChI 1S C2H3ClO2 c1 5 2 3 4 h1H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey XMJHPCRAQCTCFT UHFFFAOYSA N Section2 Chembox Properties C 2 H 3 Cl 1 O 2 Density 1.223 g mL MeltingPt BoilingPt 70 72 C Section7 Chembox Hazards EUClass Hazchem C Hazchem N Hazchem Xn ExternalMSDS EUIndex RPhrases R34 R50 53 SPhrases S1 2 S26 S45 S60 S61 FlashPt 10 C Methyl chloroformate is the methyl ester of chloroformic acid . It is also known as methyl chlorocarbonate, and is an oily liquid with a colour that is anywhere from yellow to colorless. It is also known for its pungent odour. Methyl chloroformate, if heated, releases phosgene and produces toxic, corrosive fumes if it comes in contact with water. Methyl chloroformate is used in organic synthesis for the introduction of the methoxycarbonyl functionality to a suitable nucleophile . References reflist Category Methyl esters Category Chloroformates Category Reagents for organic chemistry ester stub de Chlorameisens uremethylester fa it Metilcloroformiato nl Methylchloorformiaat fi Metyyliklooriformiaatti ... more details
Chembox Watchedfields changed verifiedrevid 416384957 ImageFile Manganocene.svg ImageSize ImageAlt IUPACName PIN OtherNames Section1 Chembox Identifiers CASNo 73138 26 8 PubChem 24199707 SMILES Section2 Chembox Properties C 10 H 10 Mn 1 Appearance Density MeltingPt 175 C BoilingPt 245 C Solubility Section3 Chembox Hazards MainHazards EUClass Hazchem Xn Hazchem F RPhrases R11 , R14 , R20 21 22 , R36 37 38 SPhrases S16 , S26 , S36 37 39 NFPA H NFPA F 2 NFPA R FlashPt 52 C 125.6 F Autoignition Unreferenced date April 2011 Manganocene or bis cyclopentadienyl manganese II is an organometallic compound of manganese . It is a metallocene . In the solid state, manganocene adopts a polymeric structure with every manganese atom coordinated by three cyclopentadienyl ligands, two of which are bridging ligands. This compound has an electron count of 17 it is readily reduced to Cp sub 2 sub Mn sup &minus sup , which has an ideal electron count of 18 see 18 electron rule . This metallocene is commercially available. It may be prepared in the conventional fashion, by reaction of manganese II chloride with sodium cyclopentadienide MnCl sub 2 sub 2 CpNa &rarr Cp sub 2 sub Mn 2 NaCl References German Magnanocen reaction stub references Category Metallocenes Category Organomanganese compounds de Manganocen ... more details
Unreferenced date February 2007 Chembox ImageFileL1 Acetone d6.png ImageFileL1 Ref chemboximage correct ?? ImageSizeL1 121 ImageNameL1 Skeletal formula of deuterated acetone ImageFileR1 Acetone 3D vdW.png ImageFileR1 Ref chemboximage correct ?? ImageSizeR1 121 ImageNameR1 Spacefill model of deuterated acetone ImageFile2 Acetone 3D balls.png ImageFile2 Ref chemboximage correct ?? ImageSize2 121 ImageName2 Skeletal formula of deuterated acetone Section1 Chembox Identifiers CASNo 666 52 4 PubChem 522220 PubChem Ref Pubchemcite correct pubchem ChemSpiderID 455535 ChemSpiderID Ref chemspidercite correct chemspider EINECS 211 563 9 UNNumber 1090 Beilstein 1702935 SMILES 2H C 2H 2H C O C 2H 2H 2H StdInChI 1S C3H6O c1 3 2 4 h1 2H3 i1D3,2D3 StdInChI Ref stdinchicite correct chemspider StdInChIKey CSCPPACGZOOCGX WFGJKAKNSA N StdInChIKey Ref stdinchicite correct chemspider Section2 Chembox Properties Formula C sub 3 sub sup 2 sup H sub 6 sub O MolarMass 64.1161 g mol sup 1 sup ExactMass 64.079525290 g mol sup 1 sup Density 0.872 g cm sup 3 sup MeltingPtC 94 BoilingPtC 56 VaporPressure 24.5 25.3 kPa at 20  C Section3 Chembox Hazards EUClass Hazchem F Hazchem Xi RPhrases R11 , R36 , R66 , R67 SPhrases S9 , S16 , S26 NFPA H 1 NFPA F 3 NFPA R 0 FlashPt 19  C Section4 Chembox Related OtherCpds Acetone Deuterated acetone CD sub 3 sub sub 2 sub CO is a form called a isotopologue of acetone CH sub 3 sub sub 2 sub CO in which the hydrogen atom H is replaced with deuterium heavy hydrogen isotope D . Deuterated acetone is a common solvent used in NMR spectroscopy . List of NMR solvents DEFAULTSORT Deuterated Acetone Category Deuterated solvent Organic compound stub zh ... more details
Unreferenced date February 2007 Chembox verifiedrevid 430465662 ImageFileL1 Deuterated benzene.svg ImageFileL1 Ref chemboximage correct ?? ImageSizeL1 121 ImageNameL1 Kekul , skeletal formula of deuterated benzene ImageFileR1 Benzene 3D vdW.png ImageFileR1 Ref chemboximage correct ?? ImageSizeR1 121 ImageNameR1 Spacefill model of deuterated benzene ImageFile2 Benzene aromatic 3D balls.png ImageFile2 Ref chemboximage correct ?? ImageSize2 121 ImageName2 Ball and stick model of deuterated benzene Section1 Chembox Identifiers CASNo 1076 43 3 PubChem 71601 PubChem Ref Pubchemcite correct pubchem ChemSpiderID 64671 ChemSpiderID Ref chemspidercite correct chemspider EINECS 214 061 8 UNNumber 1114 Beilstein 1905426 SMILES 2H c1c 2H c 2H c 2H c 2H c1 2H StdInChI Ref stdinchicite correct chemspider StdInChI 1S C6H6 c1 2 4 6 5 3 1 h1 6H i1D,2D,3D,4D,5D,6D StdInChIKey Ref stdinchicite correct chemspider StdInChIKey UHOVQNZJYSORNB MZWXYZOWSA N Section2 Chembox Properties Formula C sub 6 sub sup 2 sup H sub 6 sub MolarMass 84.1488 g mol sup &minus 1 sup ExactMass 84.084610668 g mol sup &minus 1 sup Density 0.950 g cm sup &minus 3 sup MeltingPtK 280 BoilingPtK 345 Section3 Chembox Thermochemistry HeatCapacity 152.46 J K sup &minus 1 sup mol sup &minus 1 sup Section4 Chembox Hazards EUClass Hazchem F Hazchem T RPhrases R45 , R46 , R11 , R36 38 , R48 23 24 25 , R65 SPhrases S53 , S45 NFPA H 2 NFPA F 3 NFPA R 0 FlashPt &minus 11 C Section5 Chembox Related OtherCpds Benzene Deuterated benzene C sub 6 sub D sub 6 sub , is a form called an isotopologues isotopologue of benzene C sub 6 sub H sub 6 sub in which the hydrogen atom H is replaced with deuterium heavy hydrogen isotope D . Deuterated benzene is a common solvent used in NMR spectroscopy . List of NMR solvents DEFAULTSORT Deuterated Benzene Category Deuterated solvent Organic compound stub zh ... more details
Unreferenced date February 2007 Chembox ImageFile Deuterated methanol.svg ImageFile Ref chemboximage correct ?? ImageSize 121 ImageName Stereo skeletal formula of deuterated methanol Section1 Chembox Identifiers CASNo 811 98 3 PubChem 71568 PubChem Ref Pubchemcite correct pubchem ChemSpiderID 64640 ChemSpiderID Ref chemspidercite correct chemspider EINECS 212 378 6 UNNumber 1230 Beilstein 1733278 SMILES 2H OC 2H 2H 2H StdInChI 1S CH4O c1 2 h2H,1H3 i1D3,2D StdInChI Ref stdinchicite correct chemspider StdInChIKey OKKJLVBELUTLKV MZCSYVLQSA N StdInChI Ref stdinchicite correct chemspider Section2 Chembox Properties Formula C sup 2 sup H sub 4 sub O MolarMass 36.0665 g mol sup 1 sup ExactMass 36.051321734 g mol sup 1 sup Density 0.888 g cm sup 3 sup MeltingPtC 98 BoilingPtC 65 Section3 Chembox Thermochemistry HeatCapacity 87.9 J K sup 1 sup mol sup 1 sup Section4 Chembox Hazards EUClass Hazchem F Hazchem T RPhrases R11 , R23 24 25 , R39 23 24 25 SPhrases S7 , S16 , S36 37 , S45 FlashPt 11 C Section5 Chembox Related OtherCpds Methanol Deuterated methanol CD sub 3 sub OD , is a form called an isotopologue of methanol CH sub 3 sub OH in which the hydrogen atom H is replaced with deuterium heavy hydrogen isotope D . Deuterated methanol is a common solvent used in NMR spectroscopy . Organic compound stub List of NMR solvents Category Deuterated solvent zh ... more details
Chembox verifiedrevid 427151664 ImageFile Pinacolone.PNG ImageFile Ref Chemboximage correct ?? ImageSize 121 ImageName Skeletal formula of pinacolone IUPACName 3,3 Dimethyl 2 butanone OtherNames t Butyl methyl ketone br 1,1,1 Trimethylacetone Section1 Chembox Identifiers CASNo 75 97 8 CASNo Ref cascite correct CAS PubChem 6416 PubChem Ref Pubchemcite correct PubChem ChemSpiderID 6176 ChemSpiderID Ref chemspidercite correct chemspider EINECS 200 920 4 UNNumber 1224 MeSHName Pinacolone RTECS EL7700000 Beilstein 1209331 SMILES CC O C C C C StdInChI 1S C6H12O c1 5 7 6 2,3 4 h1 4H3 StdInChI Ref stdinchicite correct chemspider StdInChIKey PJGSXYOJTGTZAV UHFFFAOYSA N StdInChIKey Ref stdinchicite correct chemspider Section2 Chembox Properties C 6 H 12 O 1 ExactMass 100.088815006 g mol sup 1 sup Appearance Colorless liquid Density 0.801 g cm sup 3 sup MeltingPtC 10 BoilingPtCL 103 BoilingPtCH 106 Section3 Chembox Hazards ExternalMSDS https fscimage.fishersci.com msds 83026.htm External MSDS EUClass Hazchem F Hazchem Xn RPhrases R11 , R22 SPhrases S9 , S16 , S29 , S33 NFPA H 1 NFPA F 4 NFPA R 0 FlashPt 5 C Pinacolone 3,3 dimethyl 2 butanone is an important ketone in organic chemistry . It has an odour reminiscent of peppermint and was discovered in 1866. Its primary use is in the synthesis of triazolylpinacolone in the synthesis of the fungicide triadimefon and in synthesis of the herbicide metribuzin . Preparation Pinacolone may be prepared via the pinacol rearrangement of pinacol , e.g. by heating with sulfuric acid ref OrgSynth author G. A. Hill and E. W. Flosdorf title Pinacolone prep CV1P0462 collvol 1 collvolpages 462 year 1941 ref File 800px Pinacol rearragement.png 500px References Reflist Ketone stub Category Ketones de 3,3 Dimethyl 2 butanon fa it Pinacolone ja zh ... more details
Unreferenced date October 2011 Chembox Section1 Chembox Identifiers CASNo 16448 28 5 CASNo Ref cascite correct ?? EINECS 231 847 6 SMILES O. OH2 Cu 1 OH2 OS O O O1 SMILES1 O. OH2 . OH2 . Cu 4 . O S O O O StdInChI 1S Cu.H2O4S.3H2O c 1 5 2,3 4 h H2,1,2,3,4 3 1H2 q 2 p 2 StdInChI Ref stdinchicite correct chemspider StdInChIKey XRZJYOVMWCUNER UHFFFAOYSA L StdInChIKey Ref stdinchicite correct chemspider Section2 Chembox Properties Formula Chem CuH 4 SO 6 sup sup H 2 O MolarMass 213.654 g mol sup 1 sup ExactMass 212.913024315 g mol sup 1 sup Section3 Chembox Hazards GHSPictograms GHS exclamation mark GHS environment GHSSignalWord WARNING HPhrases H phrases 302 319 315 410 PPhrases P phrases 264 270 273 280 301 312 302 352 305 351 338 321 330 332 313 337 313 362 501 EUIndex 029 004 00 0 EUClass Hazchem Xn Hazchem N RPhrases R22 , R36 38 , R50 53 SPhrases S2 , S22 , S60 , S61 Copper II sulfate trihydrate , also known as cupric sulfate trihydrate , is the chemical compound with the chemical formula copper Cu sulfate SO sub 4 sub .3 properties of water H sub 2 sub O . This hydrated salt is one less commonly encountered copper II sulfate copper sulfate salts. It dehydrates above Convert 109 C F . Copper II sulfate trihydrate occurs naturally as bonattite. Category Copper compounds Inorganic compound stub fa II ... more details
chembox verifiedrevid 415462460 ImageFile Chloroacetyl chloride.svg ImageSize 150px ImageName Skeletal formula ImageFile1 Chloroacetyl chloride 3D balls.png ImageSize1 170px ImageName1 ball and stick model IUPACName chloroacetyl chloride OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 6329 CASNo 79 04 9 CASNo Ref cascite PubChem 6577 SMILES C C O Cl Cl EINECS 201 171 6 KEGG Ref keggcite correct kegg KEGG C14859 Section2 Chembox Properties C 2 H 2 Cl 2 O 1 Appearance Colorless liquid Density 1.42 g mL MeltingPtC 22 BoilingPtC 106 Solubility Reacts Section3 Chembox Hazards ExternalMSDS http msds.chem.ox.ac.uk CH chloroacetyl chloride.html Oxford MSDS EUClass Hazchem T Hazchem N Hazchem C FlashPt Autoignition Chloroacetyl chloride is a chlorinated acyl chloride . It is a bifunctional bifunctional compound , making it a useful building block chemical. Production Industrially, it is produced by the carbonylation of methylene chloride , oxidation of vinylidene chloride , or the addition of chlorine to ketene . ref name worsham cite book editor Zoeller, Joseph R. Agreda, V. H., eds. title Acetic acid and its derivatives publisher M. Dekker location New York year 1993 chapter 15. Halogenated Derivatives author Paul R. Worsham isbn 0 8247 8792 7 pages 288 298 url http books.google.com ?id 3MjdGp1v1YIC&pg RA2 PA288 format Google Books excerpt ref It may be prepared from chloroacetic acid and thionyl chloride , phosphorus pentachloride , or phosgene . Reactions Chloroacetyl chloride is bifunctional the acyl chloride easily forms ester s ref OrgSynth prep cv3p0141 collvol 3 collvolprep 141 year 1955 title tert Butyl acetate author Robert H. Baker and Frederick G. Bordwell ref and amide s, while the other end of the molecule is able to form other linkages, e.g. with amines. The use of chloroacetyl chloride in the synthesis of lidocaine is illustrative ref cite journal journal J. Chem. Ed. volume 76 issue 11 year 1999 pages ... more details