1,5-i-aedans

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Names

[ CAS No. ]:
36930-63-9

[ Name ]:
1,5-i-aedans

[Synonym ]:
5-(iodoacetylaminoethyl)amino-naphthalene-1-sulphonic acid
5-[2-(2-iodoacetamido)ethylamino]-1-naphthalenesulfonic acid
1,5-l-AEDANS
(N-(2-iodoacetamino)ethyl)-1-naphtylamine-5-sulfonic acid
5-[2-[(2-iodoacetyl)amino]ethylamino]naphthalene-1-sulfonic acid
5-((((2-iodoacetyl)amino)ethyl)amino)-naphthalene-1-sulfonic acid
N-(Iodoacetylaminoethyl)-5-naphthylamine-1-sulfonic acid
N-(iodoacetaminoethyl)-1-naphthylamine-5-sulfonic acid
IAEDANS
N-iodoacetyl-N'-(5-sulfo-1-naphthyl)ethyl-enediamine
Hudson-Weber-Reagent
1,5-IAEDANS [N-(Iodoacetaminoethyl)-1-naphthylamine-5-sulfonic acid]
EINECS 253-277-7
MFCD00003993
1,5-I-Aedans

Chemical & Physical Properties

[ Density]:
1.808 g/cm3

[ Melting Point ]:
300ºC

[ Molecular Formula ]:
C14H15IN2O4S

[ Molecular Weight ]:
434.24900

[ Exact Mass ]:
433.98000

[ PSA ]:
103.88000

[ LogP ]:
3.59430

[ Index of Refraction ]:
1.707

[ Storage condition ]:
2-8°C

[ Stability ]:
Sensitive to Light

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Detection of proteins on blot membranes.

Curr. Protoc. Protein Sci. Chapter 10 , Unit 10.8, (2001)

Staining of blot transfer membranes permits visualization of proteins and allows the extent of transfer to be monitored. In the protocols described in this unit, proteins are stained after electroblot...

Iron-sulfur cluster biosynthesis: characterization of IscU-IscS complex formation and a structural model for sulfide delivery to the [2Fe-2S] assembly site.

J. Biol. Inorg. Chem. 14(6) , 829-39, (2009)

Recent work on the bacterial iron-sulfur cluster (isc) family of gene products, and eukaryotic homologs, has advanced the molecular understanding of cellular mechanisms of iron-sulfur cluster biosynth...

Characterization of the formation of amyloid protofibrils from barstar by mapping residue-specific fluorescence dynamics.

J. Mol. Biol. 358(4) , 935-42, (2006)

The small protein barstar aggregates at low pH to form soluble oligomers, which can be transformed into fibrillar aggregates at an elevated temperature. To characterize structurally, with residue-spec...


More Articles

Related Compounds

  • 1,5-AEDANS
  • Azidopurine
  • 3-Isoxazolemethanol,-alpha--methyl-5-(1-methylethyl)-
  • Thieno[2,3-b]pyridin-4(7H)-one
  • 1 5-CYCLOOCTADIENE-KUPFER(I)-CHLORID
  • [(1,5-cyclooctadiene)PtCl(tri-i-propylphosphine)]Cl
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • Sodium 4-chloro-2-methylbenzene-1-sulfinate
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 3-((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)-1-methylpyrazin-2(1H)-one
  • 5-Hydroxy-2-(2-methoxyethoxy)-N,N-dimethylbenzamide
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde