lissamine rhodamine b sulfonyl chloride
Names
[ CAS No. ]:
62796-29-6
[ Name ]:
lissamine rhodamine b sulfonyl chloride
[Synonym ]:
MFCD00042001
5-chlorosulfonyl-2-[3-(diethylamino)-6-diethylazaniumylidenexanthen-9-yl]benzenesulfonate
EINECS 263-735-8
Sulforhodamine B acid chloride
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
[Cell Assay]
[References]
[Related Small Molecules]
Chemical & Physical Properties
[ Density]:
1.1576 (rough estimate)
[ Molecular Formula ]:
C27H29ClN2O6S2
[ Molecular Weight ]:
577.11200
[ Exact Mass ]:
576.11600
[ PSA ]:
127.49000
[ LogP ]:
6.85600
[ Index of Refraction ]:
1.6100 (estimate)
[ Storage condition ]:
−20°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2921199090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2921199090
[ Summary ]:
2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Bioconjug. Chem. 18(4) , 1118-22, (2007)
A conjugable analogue of the benzodiazepine 4' '-chlorodiazepam (Ro5-4864), C6Ro5-4864 was synthesized to probe the binding sites of translocator protein (18 kDa; TSPO), previously known as the periph...
Local immunity to Bacteroides gingivalis in periodontal disease.J. Dent. Res. 59 , 1750-6, (1980)
The histopathologic status of gingival tissue was assessed according to the criteria of Page and Schroeder.(5) Rhodamine-labeled bacteria were used to assess the antigenic specificity of plasma cells ...
Psoralen conjugates for visualization of genomic interstrand cross-links localized by laser photoactivation.Bioconjug. Chem. 18(2) , 431-7, (2007)
DNA interstrand cross-links are formed by chemotherapy drugs as well as by products of normal oxidative metabolism. Despite their importance, the pathways of cross-link metabolism are poorly understoo...