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Safety Information

569427-U

Supelco

Discovery® C8 (5 µm) HPLC Columns

L × I.D. 12.5 cm × 4.6 mm, HPLC Column

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1 EA
¥7,189.67

¥7,189.67

Estimated to ship on2025年6月06日Details

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1 EA
¥7,189.67

About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52

¥7,189.67

Estimated to ship on2025年6月06日Details

Product Name

Discovery® C8 HPLC Column, 5 μm particle size, L × I.D. 12.5 cm × 4.6 mm

material

stainless steel column

Quality Level

100

Agency

suitable for USP L7

product line

Discovery®

feature

endcapped

manufacturer/tradename

Discovery®

packaging

1 ea of

extent of labeling

7.5% Carbon loading

parameter

≤70 °C temp. range
400 bar pressure (5801 psi)

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This Item
59354U3059353U4059353U
Discovery ® C8 HPLC 色谱柱 5 μm particle size, L × I.D. 12.5 cm × 4.6 mm

569427U

Discovery ® C8 HPLC 色谱柱

Discovery ® C8 HPLC 色谱柱 5 μm particle size, L × I.D. 25 cm × 3 mm

59354U30

Discovery ® C8 HPLC 色谱柱

Discovery ® C8 HPLC 色谱柱 5 μm particle size, L × I.D. 15 cm × 4 mm

59353U40

Discovery ® C8 HPLC 色谱柱

Discovery ® C8 HPLC 色谱柱 5 μm particle size, L × I.D. 15 cm × 4.6 mm

59353U

Discovery ® C8 HPLC 色谱柱

matrix

silica gel, high purity, spherical base material, fully porous particle

matrix

silica gel, high purity, spherical base material, fully porous particle

matrix

silica gel, high purity, spherical base material, fully porous particle

matrix

silica gel, high purity, spherical base material, fully porous particle

particle size

5 μm

particle size

5 μm

particle size

5 μm

particle size

5 μm

matrix active group

C8 (octyl) phase

matrix active group

C8 (octyl) phase

matrix active group

C8 (octyl) phase

matrix active group

C8 (octyl) phase

product line

Discovery®

product line

Discovery®

product line

Discovery®

product line

Discovery®

pore size

180 Å

pore size

180 Å

pore size

180 Å

pore size

180 Å

Features and Benefits

  • Excellent reproducibility
  • Faster separation of strongly hydrophobic analytes than C18 columns
  • Stable, low-bleed LC-MS separations
  • Exceptional peak shapes for basic and acidic compounds
  • Compatible with low organic/highly aqueous mobile phases

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Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

Discovery is a registered trademark of Merck KGaA, Darmstadt, Germany

Regulatory Information

新产品

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Certificates of Analysis (COA)

Lot/Batch Number
291217-01
284903-01
284830-01
284829-01
282823-01

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M Q Zhang et al.
Die Pharmazie, 46(10), 687-700 (1991-10-01)
The rapid growth in the quinolone research changed the whole face of the previous SAR concepts. So far structural modifications at all positions of the quinolone nucleus except the 4-oxo group have successfully lead to the discovery of potent antimicrobial
Simeon Grazio et al.
Clinical and experimental rheumatology, 31(5), 665-671 (2013-06-07)
Using proteomic approach in this study, we sought to identify proteins with heparin affinity associated with rheumatoid arthritis (RA), psoriatic arthritis (PsA) and non-inflammatory arthritis (NIA). Plasma samples from adult RA, PsA and NIA patients, 20 of each, were collected.
G L Bundy et al.
The Journal of biological chemistry, 261(2), 747-751 (1986-01-15)
The gorgonian coral Pseudoplexaura porosa contains a lipoxygenase capable of converting exogenous arachidonic acid into (8R)-8-hydroperoxy-5,9,11,14-eicosatetraenoic acid. The (8R)- (or 8-L-) configuration in this product, opposite to that observed in previously reported 8-lipoxygenase products, was determined unambiguously by comparison of
Wai Shun Mak et al.
Nature communications, 6, 10005-10005 (2015-11-26)
The ability to biosynthetically produce chemicals beyond what is commonly found in Nature requires the discovery of novel enzyme function. Here we utilize two approaches to discover enzymes that enable specific production of longer-chain (C5-C8) alcohols from sugar. The first
J Reniers et al.
European journal of medicinal chemistry, 46(12), 6104-6111 (2011-10-25)
Previous studies on 5H-indeno[1,2-c]pyridazin-5-one derivatives as inhibitors of MAO-B revealed that it was possible to increase the MAO-B inhibitory potency of 5H-indeno[1,2-c]pyridazin-5-ones by substituting the central heterocycle in the 3-position or C-8 with lipophilic groups which occupy the substrate cavity
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Discovery C18 and C8 HPLC Columns

Discovery C18 and C8 HPLC Columns products offered

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