Misplaced Pages

:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox: Difference between revisions - Misplaced Pages

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
< Misplaced Pages:WikiProject Chemicals | Chembox validation Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 12:33, 15 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 473697878 of page Allyl_alcohol for the Chem/Drugbox validation project (updated: '').← Previous edit Revision as of 12:33, 15 February 2012 edit undoBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 473697840 of page Sulfamic_acid for the Chem/Drugbox validation project (updated: '').Next edit →
Line 1: Line 1:
{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}} {{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 443376202 | verifiedrevid = 417637524
| ImageFile = Allyl-alcohol.png
| Name = Sulfamic acid
| ImageName = Skeletal formula
| ImageFile = Zwitterion Structural Formulae V.1.svg
⚫ | ImageFile1 = Allyl-alcohol-3D-balls-2.png
| ImageSize = 220px
⚫ | ImageName1 = Ball-and-stick model
| ImageName = Tautomerism of sulfamic acid
| IUPACName = Prop-2-en-1-ol, Allyl alcohol
⚫ | ImageFileL1 = Sulfamic-acid-3D-balls.png
| ImageSizeL1 = 110px
| ImageNameL1 = Ball-and-stick model of the canonical neutral form
| ImageFileR1 = Sulfamic-acid-zwitterion-3D-balls.png
| ImageSizeR1 = 110px
⚫ | ImageNameR1 = Ball-and-stick model of the zwitterionic form
| IUPACName = Sulfamic acid
| Section1 = {{Chembox Identifiers | Section1 = {{Chembox Identifiers
| KEGG_Ref = {{keggcite|correct|kegg}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| KEGG = C02001 | ChemSpiderID = 5767
| PubChem = 5987
| InChIKey = XXROGKLTLUQVRX-UHFFFAOYAC
⚫ | InChI = 1/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)
| InChIKey = IIACRCGMVDHOTQ-UHFFFAOYAK
⚫ | ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 9330
⚫ | SMILES = O=S(=O)(O)N
| ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 234926 | ChEMBL = 68253
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C3H6O/c1-2-3-4/h2,4H,1,3H2 | StdInChI = 1S/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = XXROGKLTLUQVRX-UHFFFAOYSA-N | StdInChIKey = IIACRCGMVDHOTQ-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}} | CASNo = 5329-14-6
| CASNo_Ref = {{cascite|correct|CAS}}
| UNNumber = 2967
| CASNo=107-18-6
| EINECS = 226-218-8
⚫ | ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 16605 | RTECS = WO5950000
}}
⚫ | SMILES = C=CCO
⚫ | Section2 = {{Chembox Properties
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| Formula = H<sub>3</sub>NSO<sub>3</sub>
| ChemSpiderID=13872989
| MolarMass = 97.10 g/mol
⚫ | InChI=1/C3H6O/c1-2-3-4/h2,4H,1,3H2}}
⚫ | MeltingPt = 205 °C decomp.
⚫ |Section2 = {{Chembox Properties
| Density = 2.15 g/cm<sup>3</sup>
| C = 3 | H = 6 | O = 1
| Solubility = moderate, with slow hydrolysis
| Density=0.854 g/ml
| pKa = 1.0<ref>{{cite doi|10.1039/JR9600004236}}</ref>
⚫ | MeltingPt=&minus;129 °C
}}
| BoilingPt=97 °C
⚫ | Section7 = {{Chembox Hazards
| Solubility=Miscible
| ExternalMSDS =
| Solvent=Water
⚫ | EUIndex = 016-026-00-0
| EUClass = Irritant ('''Xi''')
| RPhrases = {{R36/38}} {{R52/53}}
⚫ | SPhrases = {{S2}} {{S26}} {{S28}} {{S61}}
⚫ | NFPA-H =
⚫ | NFPA-F =
⚫ | NFPA-R =
| NFPA-O =
⚫ | FlashPt =
}}
| Section8 = {{Chembox Related
| OtherAnions =
| OtherCations = ]
| OtherFunctn =
| Function =
| OtherCpds =
}} }}
⚫ |Section3={{Chembox Hazards
| EUClass=Toxic ('''T''')<br />Dangerous for<br />the environment ('''N''')
⚫ | EUIndex=603-015-00-6
| ExternalMSDS =
⚫ | NFPA-H=3
⚫ | NFPA-F=3
⚫ | NFPA-R=0
| RPhrases={{R10}}, {{R23/24/25}},<br />{{R36/37/38}}, {{R50}}
⚫ | SPhrases={{S1/2}}, {{S36/37/39}},<br />{{S38}}, {{S45}}, {{S61}}
⚫ | FlashPt=21 °C
| Autoignition=378 °C
| ExploLimits=2.5&ndash;18.0%}}
}} }}

Revision as of 12:33, 15 February 2012

This page contains a copy of the infobox ({{chembox}}) taken from revid 473697840 of page Sulfamic_acid with values updated to verified values.
Sulfamic acid
Tautomerism of sulfamic acid
Ball-and-stick model of the canonical neutral form
Ball-and-stick model of the canonical neutral form
Ball-and-stick model of the zwitterionic form
Ball-and-stick model of the zwitterionic form
Names
IUPAC name Sulfamic acid
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
EC Number
  • 226-218-8
PubChem CID
RTECS number
  • WO5950000
UN number 2967
InChI
  • InChI=1S/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)Key: IIACRCGMVDHOTQ-UHFFFAOYSA-N
  • InChI=1/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)Key: IIACRCGMVDHOTQ-UHFFFAOYAK
SMILES
  • O=S(=O)(O)N
Properties
Chemical formula H3NSO3
Molar mass 97.10 g/mol
Density 2.15 g/cm
Melting point 205 °C decomp.
Solubility in water moderate, with slow hydrolysis
Acidity (pKa) 1.0
Related compounds
Other cations Ammonium sulfamate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Tracking categories (test):
Chemical compound
  1. Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1039/JR9600004236, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with |doi=10.1039/JR9600004236 instead.