Quality Level
grade
Molecular Biology
description
non-ionic
form
liquid
technique(s)
IR spectroscopy: suitable
CMC
0.08 mM (20-25°C)
viscosity
~250-350 cP(25 °C)
mp
6 °C
solubility
water: soluble at 20 °C
density
1.060 g/cm3
HLB
13
foreign activity
DNase and RNase, none detected
SMILES string
O(CCO)c1ccc(cc1)C(CC(C)(C)C)(C)C
InChI
1S/C16H26O2/c1-15(2,3)12-16(4,5)13-6-8-14(9-7-13)18-11-10-17/h6-9,17H,10-12H2,1-5H3
InChI key
JYCQQPHGFMYQCF-UHFFFAOYSA-N
General description
IGEPAL® CA-630 is a nonionic, non-denaturing detergent suitable for solubilization, isolation and purification of membrane protein complexes.It is chemically indistinguishable from Nonidet P-40.
Application
IGEPAL® CA-630 has been used
- as neutral detergent in homogenizing buffer during western blotting of mouse muscle homogenates
- In X-gal staining for studying the lacZ expression in E8.5-E10.5 embryos
- In Cell-Lysis (CL) buffer for preparing RT-qPCR-ready cell lysates
Analysis Note
Chemically indistinguishable from Nonidet P-40, which is no longer commercially available.
Other Notes
Nonionic, non-denaturing detergent
Legal Information
IGEPAL is a registered trademark of Solvay
Disclaimer
May develop turbidity or sediment during storage. A clear liquid can be obtained on heating to 40°C.
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signalword
Danger
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
483.8 °F - closed cup
flash_point_c
251 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - ED ENV 1 - Eye Dam. 1 - Skin Irrit. 2
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Amina Abbadi et al.
The Journal of biological chemistry, 291(3), 1448-1455 (2015-11-26)
Many cells, including murine airway epithelial cells, respond to a variety of inflammatory stimuli by synthesizing leukocyte-adhesive hyaluronan (HA) cables that remain attached to their cell surfaces. This study shows that air-liquid interface cultures of murine airway epithelial cells (AECs)
Kenneth Shatzkes et al.
Scientific reports, 4, 4659-4659 (2014-04-12)
Sample nucleic acid purification can often be rate-limiting for conventional quantitative PCR (qPCR) workflows. We recently developed high-throughput virus microneutralization assays using an endpoint assessment approach based on reverse transcription qPCR (RT-qPCR). The need for cumbersome RNA purification is circumvented
Bojana Lucic et al.
Nature communications, 10(1), 4059-4059 (2019-09-08)
HIV-1 recurrently targets active genes and integrates in the proximity of the nuclear pore compartment in CD4+ T cells. However, the genomic features of these genes and the relevance of their transcriptional activity for HIV-1 integration have so far remained


