Octyl Sepharose 4FF

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Names

[ CAS No. ]:
68652-09-5

[ Name ]:
Octyl Sepharose 4FF

[Synonym ]:
N-[Methoxy(phenyl)acetyl]-5-nitrilonorvaline
Norvaline, N-(2-methoxy-2-phenylacetyl)-5-nitrilo-
Octyl Sepharose 4FF
Octyl-agarose

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
563.0±50.0 °C at 760 mmHg

[ Molecular Formula ]:
C14H16N2O4

[ Molecular Weight ]:
276.288

[ Flash Point ]:
294.3±30.1 °C

[ Exact Mass ]:
276.110992

[ LogP ]:
0.99

[ Appearance of Characters ]:
saline suspension

[ Vapour Pressure ]:
0.0±1.6 mmHg at 25°C

[ Index of Refraction ]:
1.545

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225

[ Precautionary Statements ]:
P210

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
F

[ Risk Phrases ]:
10-11

[ Safety Phrases ]:
S7-16

[ RIDADR ]:
UN 1170 3/PG 3

[ WGK Germany ]:
3

[ Hazard Class ]:
10-11

Articles

An improved methodology to produce Flavobacterium heparinum chondroitinases, important instruments for diagnosis of diseases.

Biotechnol. Appl. Biochem. 37(2) , 115-127, (2003)

Chondroitinases are very important tools for the identification and structural analysis of proteoglycans. Enzymic analysis with Flavobacterium heparinum chondroitinases has shown that chondroitin sulp...

Purification, characterization, molecular cloning, and expression of a new aminoacylase from Streptomyces mobaraensis that can hydrolyze N-(middle/long)-chain-fatty-acyl-L-amino acids as well as N-short-chain-acyl-L-amino acids.

Biosci. Biotechnol. Biochem. 73(9) , 1940-1947, (2009)

We report here on the purification, characterization, molecular cloning, and expression of a new aminoacylase, initially isolated from the supernatant of Streptomyces mobaraensis (Sm-AA). Purified wil...

Characterization and partial purification of the rat and human enzyme systems active in the reduction of N-hydroxymelagatran and benzamidoxime.

Drug Metab. Dispos. 33(4) , 570-578, (2005)

The enzymic basis for intracellular reduction of N-hydroxylated amidines to their corresponding amidines, and hydroxylamines to their corresponding amines, is unknown. The hydroxylated amidines can be...


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Related Compounds

  • octyl-phenyl-phosphinic acid ethyl ester
  • octyl 3-(4-methoxyphenyl)prop-2-enoate
  • octyl 2-(4-chloroanilino)-2-oxoacetate
  • octyl 2-(benzamido)acetate
  • Octyl-α-hydroxyglutarate
  • octyl dihydrogen phosphate, compound with 2,2'-iminodiethanol (1:1)