Trichome

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CheMoBot (talk | contribs)
Updating {{chembox}} (changes to verified and watched fields) per Chem/Drugbox validation (report errors or bugs)
203.153.198.190 (talk)
Added relevant citations in the field for each of the two major use-case claims. They were correct, but uncited, and this compound is niche enough that proper citations are probably for the best.
 
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| Watchedfields = changed
| Watchedfields = changed
| verifiedrevid = 401248657
| verifiedrevid = 401248657
| ImageFile = Amido Black.svg
| ImageFile = Amido black new.svg
| ImageSize = 320px
| ImageSize = 320px
| Reference = <ref>{{cite web | url = http://www.chemicalland21.com/specialtychem/finechem/AMIDO%20BLACK%2010B.htm | title = AMIDO BLACK 10B | publisher = chemicalland21.com | accessdate = December 2, 2017}}</ref><!-- synonym list is derived from this reference -->
| ImageFile1 = Amido-black-10B-sodium-3D-spacefill.png
| IUPACName = Sodium 4-amino-5-hydroxy-3-((''E'')-(4-nitrophenyl)diazenyl)-6-((''E'')-phenyldiazenyl)naphthalene-2,7-disulfonate
| ImageSize1 = 280
| OtherNames = 4-Amino-5-hydroxy-3-[(4-nitrophenyl)azo]-6-(phenylazo)-2,7-naphthalene disulfonic acid, disodium salt<br />Amidoschwarz<br />Naphthol blue black<br />Acid Black 1<br />Acidal Black 10B<br />Acidal Navy Blue 3BR<br />Naphthalene Black 10B <br />Buffalo Black NBR<br />C.I. 20470
| ImageAlt1 = Space-filling model of the amido black 10B molecule
| IUPACName = <nowiki>4-Amino-5-hydroxy-3-[(4-nitrophenyl)azo]-6- -(phenylazo)-2,7-Naphthalene disulfonic acid, disodium salt</nowiki>
| OtherNames = Amidoschwarz <br /> Naphthol blue black <br /> Acid Black 1 <br /> Acidal Black 10B <br /> Acidal Navy Blue 3BR <br /> Naphthalene Black 10B (see [[Talk:Amido black 10B|talk page]]) <br /> Buffalo Black NBR <br /> C.I. 20470
|Section1={{Chembox Identifiers
|Section1={{Chembox Identifiers
| InChI = 1/C22H16N6O9S2.2Na/c23-19-18-12(11-17(39(35,36)37)21(22(18)29)27-24-13-4-2-1-3-5-13)10-16(38(32,33)34)20(19)26-25-14-6-8-15(9-7-14)28(30)31;;/h1-11,29H,23H2,(H,32,33,34)(H,35,36,37);;/q;2*+1/p-2/b26-25+,27-24+;;
| InChI = 1/C22H16N6O9S2.2Na/c23-19-18-12(11-17(39(35,36)37)21(22(18)29)27-24-13-4-2-1-3-5-13)10-16(38(32,33)34)20(19)26-25-14-6-8-15(9-7-14)28(30)31;;/h1-11,29H,23H2,(H,32,33,34)(H,35,36,37);;/q;2*+1/p-2/b26-25+,27-24+;;
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| CASNo_Ref = {{cascite|correct|??}}
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 1064-48-8
| CASNo = 1064-48-8
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = SZT789770M
| PubChem = 9566044
| PubChem = 9566044
| EINECS = 213-903-1
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 10660833
| ChemSpiderID = 10660833
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 86230
| ChEBI = 86230
| SMILES = [Na+].[Na+].O=N(=O)c1ccc(cc1)/N=N/c2c(N)c4c(cc2S([O-])(=O)=O)cc(c(/N=N/c3ccccc3)c4O)S([O-])(=O)=O
| SMILES = [Na+].[Na+].O=N(=O)c1ccc(cc1)/N=N/c2c(N)c4c(cc2S([O-])(=O)=O)cc(c(/N=N/c3ccccc3)c4O)S([O-])(=O)=O
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| MeltingPt =
| MeltingPt =
| BoilingPt =
| BoilingPt =
| Solubility = ~ 30 g/l at {{convert|20|C}}
| Solubility = ~ 30 g/L at {{convert|20|C}}
}}
}}
|Section7={{Chembox Hazards
|Section7={{Chembox Hazards
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| NFPA-F = 0
| NFPA-F = 0
| NFPA-R = 0
| NFPA-R = 0
| RPhrases = {{R20}}, {{R21}}, {{R33}}
| GHSPictograms = {{GHS07}}
| GHSSignalWord = Warning
| SPhrases = {{S28}}A, {{S37}}, {{S45}}
| HPhrases =
| PPhrases =
}}
}}
}}
}}


'''Amido black 10B''' is an [[amino acid]] [[staining]] [[diazo dye]] used in biochemical research to stain for total [[protein]] on transferred membrane blots. It is also used in criminal investigations to detect [[blood]] present with latent [[fingerprint]]s. It stains the proteins in blood a blue-black color. Amido Black can be either [[methanol]] or water based as it readily dissolves in both. With [[picric acid]], in a [[van Gieson]] procedure, it can be used to stain [[collagen]] and [[reticulin]].
'''Amido black 10B''' is an [[amino acid]] [[staining]] [[azo dye]] used in biochemical research to stain for total [[protein]] on transferred membrane blots, such as the [[western blot]].<ref>Kurien, B. T., & Scofield, R. H. (2015). Western Blotting: An Introduction. In B. T. Kurien & R. H. Scofield (Eds.), Western Blotting: Methods and Protocols (pp. 17–30). Springer. {{ISBN|978-1-4939-2694-7}}</ref> It is also used in criminal investigations to detect [[blood]] present with latent [[fingerprint]]s - it stains the proteins in blood a blue-black color.<ref>Bossers, L. C. A. M., Roux, C., Bell, M., & McDonagh, A. M. (2011). Methods for the enhancement of fingermarks in blood. Forensic Science International, 210(1), 1–11. {{doi|10.1016/j.forsciint.2011.04.006}}</ref> Amido Black can be either [[methanol]] or water based as it readily dissolves in both. With [[picric acid]], in a [[van Gieson]] procedure, it can be used to stain [[collagen]] and [[reticulin]].

==See also==
*[[Western blot normalization]]

==References==
{{reflist}}


==External links==
==External links==
*[https://web.archive.org/web/20071011133532/http://ptcl.chem.ox.ac.uk/MSDS/AM/amido_black_10B.html MSDS at Oxford University]
*[http://www.chemicalland21.com/specialtychem/finechem/AMIDO%20BLACK%2010B.htm www.chemicalland21.com]

*[http://ptcl.chem.ox.ac.uk/MSDS/AM/amido_black_10B.html MSDS at Oxford University]
{{Glutamate metabolism and transport modulators}}


{{DEFAULTSORT:Amido Black 10b}}
{{DEFAULTSORT:Amido Black 10b}}
[[Category:Azo dyes]]
[[Category:Azo dyes]]
[[Category:Naphthalenesulfonates]]
[[Category:Naphthalenesulfonates]]
[[Category:Sodium compounds]]
[[Category:Organic sodium salts]]
[[Category:1-Naphthols]]
[[Category:1-Naphthols]]
[[Category:Nitrobenzenes]]
[[Category:Nitrobenzene derivatives]]
[[Category:Aromatic amines]]
[[Category:Aromatic amines]]
[[Category:Acid dyes]]

Latest revision as of 04:46, 9 April 2024

Amido black 10B[1]
Names
IUPAC name
Sodium 4-amino-5-hydroxy-3-((E)-(4-nitrophenyl)diazenyl)-6-((E)-phenyldiazenyl)naphthalene-2,7-disulfonate
Other names
4-Amino-5-hydroxy-3-[(4-nitrophenyl)azo]-6-(phenylazo)-2,7-naphthalene disulfonic acid, disodium salt
Amidoschwarz
Naphthol blue black
Acid Black 1
Acidal Black 10B
Acidal Navy Blue 3BR
Naphthalene Black 10B
Buffalo Black NBR
C.I. 20470
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.012.640 Edit this at Wikidata
EC Number
  • 213-903-1
UNII
  • InChI=1S/C22H16N6O9S2.2Na/c23-19-18-12(11-17(39(35,36)37)21(22(18)29)27-24-13-4-2-1-3-5-13)10-16(38(32,33)34)20(19)26-25-14-6-8-15(9-7-14)28(30)31;;/h1-11,29H,23H2,(H,32,33,34)(H,35,36,37);;/q;2*+1/p-2/b26-25+,27-24+;; checkY
    Key: AOMZHDJXSYHPKS-DROYEMJCSA-L checkY
  • InChI=1/C22H16N6O9S2.2Na/c23-19-18-12(11-17(39(35,36)37)21(22(18)29)27-24-13-4-2-1-3-5-13)10-16(38(32,33)34)20(19)26-25-14-6-8-15(9-7-14)28(30)31;;/h1-11,29H,23H2,(H,32,33,34)(H,35,36,37);;/q;2*+1/p-2/b26-25+,27-24+;;
    Key: AOMZHDJXSYHPKS-NJAWIMKDBA
  • [Na+].[Na+].O=N(=O)c1ccc(cc1)/N=N/c2c(N)c4c(cc2S([O-])(=O)=O)cc(c(/N=N/c3ccccc3)c4O)S([O-])(=O)=O
Properties
C22H14N6Na2O9S2
Molar mass 616.49 g·mol−1
Appearance Dark red to black
~ 30 g/L at 20 °C (68 °F)
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
0
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Amido black 10B is an amino acid staining azo dye used in biochemical research to stain for total protein on transferred membrane blots, such as the western blot.[2] It is also used in criminal investigations to detect blood present with latent fingerprints - it stains the proteins in blood a blue-black color.[3] Amido Black can be either methanol or water based as it readily dissolves in both. With picric acid, in a van Gieson procedure, it can be used to stain collagen and reticulin.

See also[edit]

References[edit]

  1. ^ "AMIDO BLACK 10B". chemicalland21.com. Retrieved December 2, 2017.
  2. ^ Kurien, B. T., & Scofield, R. H. (2015). Western Blotting: An Introduction. In B. T. Kurien & R. H. Scofield (Eds.), Western Blotting: Methods and Protocols (pp. 17–30). Springer. ISBN 978-1-4939-2694-7
  3. ^ Bossers, L. C. A. M., Roux, C., Bell, M., & McDonagh, A. M. (2011). Methods for the enhancement of fingermarks in blood. Forensic Science International, 210(1), 1–11. doi:10.1016/j.forsciint.2011.04.006

External links[edit]

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