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139564

Sigma-Aldrich

1,2,7,8-Diepoxyoctan

97%

Synonym(e):

1,7-Octadiene bisoxide, 1,7-Octadiene diepoxide, 2,2′-(1,4-Butanediyl)bis[oxirane]

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About This Item

Empirische Formel (Hill-System):
C8H14O2
CAS-Nummer:
2426-07-5
Molekulargewicht:
142.20
EG-Nummer:
219-375-9
MDL-Nummer:
MFCD00005155
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24848422
NACRES:
NA.23

Qualitätsniveau

200

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.445 (lit.)

bp

240 °C (lit.)

Dichte

0.997 g/mL at 25 °C (lit.)

SMILES String

C(CCC1CO1)CC2CO2

InChI

1S/C8H14O2/c1(3-7-5-9-7)2-4-8-6-10-8/h7-8H,1-6H2

InChIKey

LFKLPJRVSHJZPL-UHFFFAOYSA-N

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Anwendung

  • Removal of GenX by APTES functionalized diepoxyoctane cross-linked chitosan beads: Cross-linked and aminated chitosan beads were synthesized using 1,2:7,8-diepoxyoctane and 3-aminopropyl triethoxysilane. These beads were studied for their efficiency in removing GenX, a problematic environmental pollutant, demonstrating a potential application in water treatment technologies (M Vakili, F Gholami, HM Zwain, W Wang… - Journal of …, 2023 - Elsevier).

Piktogramme

Skull and crossbonesHealth hazard
GHS06,GHS08

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Carc. 1B - Muta. 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

208.4 °F - closed cup

Flammpunkt (°C)

98 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
STBB0548V
S74417
S51630
S51269
STBB8620V

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X Zhao
Journal of biomaterials science. Polymer edition, 17(4), 419-433 (2006-06-14)
Hyaluronic acid (hyaluronan, HA) has many medical applications as a biomaterial. To enhance its biostability, a novel hydrogel of cross-linked hyaluronic acid was prepared using a double cross-linking process, which involves building cross-linkages between hydroxyl group pairs and carboxyl group
E H Vock et al.
Mutation research, 441(1), 85-93 (1999-05-04)
The time-dependent dose-response relationships for the induction of DNA double-strand breaks (DSB) assessed by pulsed-field gel electrophoresis (PFGE) and for viability (evaluated by the MTT cytotoxicity test) were investigated in order to discriminate between genotoxic and cytotoxic mechanisms of DNA
A H al-Hakim et al.
The Biochemical journal, 251(3), 935-938 (1988-05-01)
A new method for the chemical labelling of nucleic acid with biotin to produce non-radioactive probes has been developed. NN'-Bis-(3-aminopropyl)butane-1,4-diamine (spermine) and long-chain diamino compounds (diaminohexane, diaminodecane and diaminododecane) were linked covalently to biotin and the resultant conjugates were attached
Cristina Pungartnik et al.
Genetics and molecular research : GMR, 1(1), 79-89 (2004-02-14)
The sensitivity responses of seven pso mutants of Saccharomyces cerevisiae towards the mutagens N-nitrosodiethylamine (NDEA), 1,2:7,8-diepoxyoctane (DEO), and 8-hydroxyquinoline (8HQ) further substantiated their allocation into two distinct groups: genes PSO1 (allelic to REV3), PSO2 (SNM1), PSO4 (PRP19), and PSO5 (RAD16)
D J Eide et al.
Molecular and cellular biology, 5(1), 1-6 (1985-01-01)
The mutation e1662 is an allele of the Caenorhabditis elegans unc-54 gene induced with the difunctional alkylating agent 1,2,7,8-diepoxyoctane. unc-54 encodes the major myosin heavy chain isozyme of body wall muscle cells. Filter-transfer hybridization and DNA sequence analysis show that
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