SBFI-AM

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Names

[ CAS No. ]:
129423-53-6

[ Name ]:
SBFI-AM

[Synonym ]:
S1148_SIAL
Sodium indicator SBFI-AM,Sodium-binding benzofuran isophthalate-AM
SBFI-AM
Sodium-binding benzofuran isophthalate-AM
Sodium indicator SBFI-AM

Chemical & Physical Properties

[ Density]:
1.311g/cm3

[ Boiling Point ]:
1110.3ºC at 760 mmHg

[ Molecular Formula ]:
C56H58N2O23

[ Molecular Weight ]:
1127.06000

[ Flash Point ]:
625.3ºC

[ Exact Mass ]:
1126.34000

[ PSA ]:
289.31000

[ LogP ]:
6.74620

[ Vapour Pressure ]:
0mmHg at 25°C

[ Index of Refraction ]:
1.567

MSDS

Safety Information

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

[ RIDADR ]:
NONH for all modes of transport

Articles

Synthetic ion transporters can induce apoptosis by facilitating chloride anion transport into cells.

Nature Chemistry 6(10) , 885-92, (2014)

Anion transporters based on small molecules have received attention as therapeutic agents because of their potential to disrupt cellular ion homeostasis. However, a direct correlation between a change...

A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy.

Blood 124(7) , 999-1009, (2014)

Studies have endeavored to reconcile whether dysfunction of neutrophils in people with cystic fibrosis (CF) is a result of the genetic defect or is secondary due to infection and inflammation. In this...

Cyclooxygenase 2 inhibitor celecoxib inhibits glutamate release by attenuating the PGE2/EP2 pathway in rat cerebral cortex endings.

J. Pharmacol. Exp. Ther. 351(1) , 134-45, (2014)

The excitotoxicity caused by excessive glutamate is a critical element in the neuropathology of acute and chronic brain disorders. Therefore, inhibition of glutamate release is a potentially valuable ...


More Articles


Related Compounds

  • SBFI-26
  • SBFI-26
  • SBFI tetraammonium
  • SBFI TETRAAMMONIUM
  • GA3-AM
  • BTC-AM
  • N,6-dimethyl-6-azaspiro[2.5]octan-1-amine
  • 5-Ethyl-3,3-dimethyl-2,3-dihydro-1H-indol-2-one
  • Hex-5-YN-1-ylhydrazine
  • 2-[[9,14,19,24,26,28,30,32,34-Nonakis(carboxymethoxy)-4-hexacyclo[21.2.2.23,6.28,11.213,16.218,21]pentatriaconta-1(25),3(35),4,6(34),8(33),9,11(32),13(31),14,16(30),18,20,23,26,28-pentadecaenyl]oxy]acetic acid
  • 2-(Difluoromethoxy)naphthalene-6-boronic acid
  • Ethyl 4-oxo-4,5-dihydropyrimidine-5-carboxylate
  • 5-[1-(2-Pyridinyl)-1h-pyrazolo[3,4-b]pyridin-4-yl]-4-pyrimidinamine
  • (6-(3-Methoxypropoxy)naphthalen-2-yl)boronic acid
  • Benzyl (2-(4-amino-3-(p-tolyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2-methylpropyl)carbamate
  • 2-(4-Chloro-3-(difluoromethoxy)phenyl)acetic acid
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