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Triton™ X-100 - for molecular biology, high purity , CAS No.9002-93-1

In stock
Item Number
T109027
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T109027-100ml
100ml
3
$49.90
T109027-500ml
500ml
2
$61.90

Basic Description

Synonyms Igepal CA-210 | CAS_118-96-7 | PDSP1_001087 | Ethanol,1,3,3-tetramethylbutyl)phenoxy]- | 2-(4-(2,4,4-Trimethylpentan-2-yl)phenoxy)ethan-1-ol | Octoxynol-1 | Triton X 305 | P-TERT-OCTYLPHENYL (2-HYDROXYETHYL)ETHER | AT25387 | Igepal CA 630 | FT-0673247 | T
Specifications & Purity for molecular biology
Biochemical and Physiological Mechanisms Widely used non-ionic surfactant for recovery of membrane components under mild non-denaturing conditions.
Legal Information Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow
Storage Temp Room temperature
Shipped In Normal
Grade for molecular biology
Product Description

General description

Triton™ X-100 is a common non-ionic surfactant and emulsifier which is often used in biochemical applications to solubilize proteins. It is considered a comparatively mild detergent, non-denaturing, and is reported in numerous references as a routinely added reagent. It is utilized for lysing cells to extract protein and cellular organelles. It can also permeabilize the living cell membrane for transfection


Application

Triton™ X-100 has been used:

• In immunohistochemistry for staining the Flat-mount retinas

• Along with ice-cold PBS (phosphate buffered saline) in suspension of cells for cell DNA analysis and Annexin V assay

• To permeabilise cells during Immunofluorescent microscopic studies

• As a positive control in LDH assay to determine the cell membrane integrity

• For estimating the lipase activity in postheparin plasma by using modified Belfrage and Vaughan radioenzymatic procedure

• For the preparation of outer membrane protein exctract

• As a component of extraction buffer along with tris-HCl, NaCl, CaCl2, ZnCl2, Brij 35 for homogenization of mice lung cells

• In the treatment of tissue sections for Immunofluorescence labeling

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Phenylpropanes
Intermediate Tree Nodes Not available
Direct Parent Phenylpropanes
Alternative Parents Phenoxy compounds  Phenol ethers  Alkyl aryl ethers  Primary alcohols  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Phenylpropane - Phenoxy compound - Phenol ether - Alkyl aryl ether - Ether - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety.
External Descriptors a small molecule

Associated Targets(Human)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HaCaT (4069 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Cruzipain (33337 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethanol
INCHI 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
InChIKey JYCQQPHGFMYQCF-UHFFFAOYSA-N
Smiles CC(C)(C)CC(C)(C)C1=CC=C(C=C1)OCCO
Isomeric SMILES CC(C)(C)CC(C)(C)C1=CC=C(C=C1)OCCO
WGK Germany 1
RTECS MD0907700
Alternate CAS 9036-19-5
PubChem CID 5590
UN Number 3082
Beilstein 2315025

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

16 results found

Lot Number Certificate Type Date Item
G2214645 Certificate of Analysis Apr 07, 2024 T109027
G2214636 Certificate of Analysis Mar 22, 2024 T109027
B2429561 Certificate of Analysis Jan 31, 2024 T109027
F2512022 Certificate of Analysis Jan 31, 2024 T109027
G2103236 Certificate of Analysis Apr 12, 2023 T109027
F2213321 Certificate of Analysis Dec 15, 2022 T109027
A2129027 Certificate of Analysis Nov 14, 2022 T109027
A2129026 Certificate of Analysis Nov 14, 2022 T109027
L2015315 Certificate of Analysis Sep 22, 2022 T109027
A2411083 Certificate of Analysis Jun 23, 2022 T109027
G2214650 Certificate of Analysis Jun 23, 2022 T109027
F2213322 Certificate of Analysis Jun 14, 2022 T109027
F2213320 Certificate of Analysis Jun 14, 2022 T109027
E2226016 Certificate of Analysis May 30, 2022 T109027
E2226013 Certificate of Analysis May 30, 2022 T109027
C2204056 Certificate of Analysis Nov 18, 2021 T109027

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Chemical and Physical Properties

Refractive Index 1.491
Flash Point(°C) 251°C
Boil Point(°C) 270°C
Melt Point(°C) 6°C
Molecular Weight 250.380 g/mol
XLogP3 4.600
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 6
Exact Mass 250.193 Da
Monoisotopic Mass 250.193 Da
Topological Polar Surface Area 29.500 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 232.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Documents & Articles

Aladdin@Guidelines for the formulation of commonly used buffers for biological experiments
Flow cytometry cell cycle analysis using propidium iodide DNA staining
Cytoskeletal Staining Reagents
CLARITY Tissue Clearing Staining Technology
Fixation and Permeabilization Protocol for Transcription Factor Flow Cytometry
Flow Cytometry Experimental Steps for Methanol Permeabilization & Triton X-100 Permeabilization
Immunofluorescence Protocol

Solution Calculators

Reviews

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