<Suppliers Price>

Triethylene glycol monododecyl ether

Names

[ CAS No. ]:
3055-94-5

[ Name ]:
Triethylene glycol monododecyl ether

[Synonym ]:
Lauryltriglycol ether
Triethylene glycol monododecyl ether
triiethylene glycol mondodecyl ether
PEG-3 Lauryl ether
Ethanol, 2-[2-[2-(dodecyloxy)ethoxy]ethoxy]-
C12E3 Dodecyl triethylene glycol ether Dodecyltriglycol Polyoxyethylene (3) lauryl ether
Dodecyltriglycol
2-{2-[2-(Dodecyloxy)ethoxy]ethoxy}ethanol
TRIETHYLENE GLYCOL MONO-N-DODECYL ETHER
triethyleneglycol monododecyl ether
Dodecyl triethylene glycol ether
Lauryl triethoxylate
MFCD00042659
Detergent Screening
EINECS 221-280-2
Triethylene glycol dodecyl ether
Triethyleneglycol monododecyl ether 1 mM
Lauryl alcohol triglycol ether

Biological Activity

[Description]:

Triethylene glycol monododecyl ether is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

[Related Catalog]:

Research Areas >> Cancer
Signaling Pathways >> PROTAC >> PROTAC Linker

[Target]

PEGs


[In Vitro]

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

[References]

[1]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-985.

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
412.0±25.0 °C at 760 mmHg

[ Molecular Formula ]:
C18H38O4

[ Molecular Weight ]:
318.492

[ Flash Point ]:
202.9±23.2 °C

[ Exact Mass ]:
318.277008

[ PSA ]:
47.92000

[ LogP ]:
4.33

[ Vapour Pressure ]:
0.0±2.2 mmHg at 25°C

[ Index of Refraction ]:
1.451

[ Storage condition ]:
2-8°C

[ Stability ]:
Stable. Combustible. Incompatible with strong oxidizing agents.

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
KK7870000
CHEMICAL NAME :
Ethanol, 2-(2-(2-(dodecyloxy)ethoxy)ethoxy)-
CAS REGISTRY NUMBER :
3055-94-5
BEILSTEIN REFERENCE NO. :
1779029
LAST UPDATED :
199701
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C18-H38-O4
MOLECULAR WEIGHT :
318.56
WISWESSER LINE NOTATION :
Q2O2O2O12

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
DNA inhibition
TEST SYSTEM :
Rodent - guinea pig Kidney
DOSE/DURATION :
10 umol/L
REFERENCE :
FCTXAV Food and Cosmetics Toxicology. (London, UK) V.1-19, 1963-81. For publisher information, see FCTOD7. Volume(issue)/page/year: 14,431,1976

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ RTECS ]:
KK7870000

[ HS Code ]:
2909499000

Synthetic Route

Customs

[ HS Code ]: 2909499000

[ Summary ]:
2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Surfactants, aromatic and isoprenoid compounds, and fatty acid biosynthesis inhibitors suppress Staphylococcus aureus production of toxic shock syndrome toxin 1.

Antimicrob. Agents Chemother. 53 , 1898-906, (2009)

Menstrual toxic shock syndrome is a rare but potentially life-threatening illness manifest through the actions of Staphylococcus aureus toxic shock syndrome toxin 1 (TSST-1). Previous studies have sho...


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.