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Sigma-Aldrich

IGEPAL® CO-630

average Mn 617

Synonym(s):

Polyoxyethylene (9) nonylphenylether, branched

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About This Item

Linear Formula:
(C2H4O)n · C15H24O · n=9-10
CAS Number:
MDL number:
UNSPSC Code:
12162002
NACRES:
NA.23

mol wt

average Mn 617

bp

250 °C (lit.)

density

1.056 g/mL at 25 °C (lit.)

HLB

13

General description

IGEPAL® CO-630 is an alkylphenol ethoxylate that is majorly used as an anionic surfactant. It belongs to the IGEPAL series of surfactants, which have hydrophobic chains. Its properties include low surface tension, low sensitivity, and biocompatibility

Application

Nonionic surfactant.

Legal Information

IGEPAL is a registered trademark of Solvay

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

EU REACH Annex XIV (Authorisation List)

CAS No.

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Wetting of TX-100 and Igepal CO-630 Surfactants on a PTFE Surface
Biswal NR and Paria S
Industrial & Engineering Chemistry Research, 50(10), 6138-6145 (2011)
Preparation of highly concentrated stable dispersions of uniform silver nanoparticles
Sondi I, et al.
Journal of Colloid and Interface Science, 260(1), 75-81 (2003)
Viktorija Herceg et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-24)
Cyclopeptidic chemotherapeutic prodrugs (cPCPs) are macromolecular protease-sensitive doxorubicin (DOX) prodrugs synthesized from a cyclodecapeptidic scaffold, termed Regioselectively Addressable Functionalized Template (RAFT). In order to increase the chemotherapeutic potential of DOX and limit its toxicity, we used a Cathepsin B (Cat
Mirko Trilling et al.
Journal of virology, 83(8), 3684-3695 (2009-02-13)
Vaccinia virus (VACV) replicates in mouse and human fibroblasts with comparable kinetics and efficiency, yielding similar titers of infectious progeny. Here we demonstrate that gamma interferon (IFN-gamma) but not IFN-alpha or IFN-beta pretreatment of mouse fibroblasts prior to VACV infection
Juliette Humeau et al.
EMBO molecular medicine, 12(5), e11622-e11622 (2020-04-24)
Chemotherapy still constitutes the standard of care for the treatment of most neoplastic diseases. Certain chemotherapeutics from the oncological armamentarium are able to trigger pre-mortem stress signals that lead to immunogenic cell death (ICD), thus inducing an antitumor immune response

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