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经验公式(希尔记法):
C8H17NO3S
化学文摘社编号:
分子量:
207.29
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
EC Number:
203-115-6
Beilstein/REAXYS Number:
2967601
MDL number:
产品名称
2-环己胺基乙磺酸, BioXtra, ≥99.0% (titration)
InChI key
MKWKNSIESPFAQN-UHFFFAOYSA-N
InChI
1S/C8H17NO3S/c10-13(11,12)7-6-9-8-4-2-1-3-5-8/h8-9H,1-7H2,(H,10,11,12)
SMILES string
OS(=O)(=O)CCNC1CCCCC1
product line
BioXtra
assay
≥99.0% (titration)
form
powder
impurities
≤0.0005% Phosphorus (P)
≤0.1% Insoluble matter
ign. residue
≤0.1%
pH
3.0-5.0 (0.5 M in H2O)
useful pH range
8.6-10.0
pKa (25 °C)
9.3
solubility
H2O: 0.5 M, clear, colorless
anion traces
chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%
cation traces
Al: ≤0.0005%
Ca: ≤0.001%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.01%
Pb: ≤0.001%
Zn: ≤0.0005%
absorption
≤0.05 at 280 in H2O at 0.5 M
≤0.08 at 260 in H2O at 0.5 M
application(s)
diagnostic assay manufacturing
Quality Level
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Application
CHES may be used:
- for pH adjustments and as a assay buffer in catechol oxidase activity measurements(32)
- as a buffer in electron paramagnetic resonance (EPR) spectroscopy and kinetic measurements(33)
- as a buffer for soil solution equivalent (SSE) yeast dextrose medium for screening pH optima for growth of Aridibacter nitratireducens A24_SHP-5_238T(34)
General description
CHES (2-(Cyclohexylamino) ethane sulfonic acid) is a derivative of amino acid taurine. It serves as a standard physiological buffer in the pH range of 8.5-9.5.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Buffers for the physiological pH range: Acidic dissociation constants of zwitterionic compounds (ACES and CHES) in water from 5 to 55? C
Roy RN, et al.
Journal of Chemical and Engineering Data, 42(1), 41-44 (1997)
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A universal nitric oxide (NO) generating surface is assembled via Layer-by-Layer (LbL) deposition of sodium alginate (Alg) and organoselenium modified polyethyleneimine (SePEI) on quartz and polymeric substrates. The immobilized SePEI species is capable of catalytically decomposing S-nitrosothiol species (RSNO) to
R C Bray et al.
Biochemistry, 39(37), 11258-11269 (2000-09-14)
Much is unknown concerning the role of thiolate ligands of molybdenum in molybdopterin enzymes. It has been suggested that thiolate dissociation from molybdenum is part of the catalytic mechanism of bis-molybdopterin enzymes of the dimethyl sulfoxide reductase (DMSOR) family. For
Hao Zhong et al.
The Analyst, 136(21), 4486-4491 (2011-09-29)
On-line concentration via Electrokinetic Supercharging (EKS) was used to enhance the sensitivity of the capillary electrophoretic separation of the four flavonoids naringenin, hesperetin, naringin and hesperidin. Separation conditions, including the background electrolyte pH and concentration, the length and choice of
A D Carraway et al.
Journal of inorganic biochemistry, 60(4), 267-276 (1995-12-01)
Electron paramagnetic resonance spectra of a number of ferric heme peptide derivatives, in aqueous-detergent and various aqueous-alcohol solvent mixtures, have been obtained using samples in the concentration range 0.1-1.0 mM. Some of these were clearly monomeric, homogeneous, mixed-ligand adducts, entirely
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