mPEG10-acetic acid - CAS 908258-58-2

m-PEG10-CH2COOH is a polyethylene glycol (PEG)-based PROTAC linker. m-PEG10-CH2COOH can be used in the synthesis of a series of PROTACs.

* Please be kindly noted that our services and products can only be used for research to organizations or companies and not intended for any clinical or individuals.

Molecular Formula
C23H46O13
Molecular Weight
530.60

mPEG10-acetic acid

    • Specification
      • Purity
        95%
        Storage
        Pure form, -20°C, 3 years; 4°C, 2 years; In solvent, -80°C, 6 months; -20°C, 1 month
        Shipping
        Room temperature in continental US; may vary elsewhere.
        IUPAC Name
        2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]acetic acid
        Synonyms
        mPEG10-CH2COOH; 2,5,8,11,14,17,20,23,26,29,32-Undecaoxatetratriacontan-34-oic acid
    • Properties
      • Boiling Point
        588.5±45.0 °C at 760 mmHg
        Density
        1.122
        InChI Key
        DNJQYLLQMMESPG-UHFFFAOYSA-N
        InChI
        InChI=1S/C23H46O13/c1-26-2-3-27-4-5-28-6-7-29-8-9-30-10-11-31-12-13-32-14-15-33-16-17-34-18-19-35-20-21-36-22-23(24)25/h2-22H2,1H3,(H,24,25)
        Canonical SMILES
        COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCC(=O)O
    • Reference Reading
      • 1.[Effects of beta glucan in highland barley on blood glucose and serum lipid in high fat-induced C57 mouse].
        Tian MJ1, Song JN, Liu PP, Su LH, Sun CH, Li Y. Zhonghua Yu Fang Yi Xue Za Zhi. 2013 Jan;47(1):55-8.
        OBJECTIVE: Study the effects of β-glucan in highland barley on blood glucose and serum lipid in high fat diet induced C57 mouse.
        2.Panobinostat plus bortezomib and dexamethasone versus placebo plus bortezomib and dexamethasone in patients with relapsed or relapsed and refractory multiple myeloma: a multicentre, randomised, double-blind phase 3 trial.
        San-Miguel JF1, Hungria VT2, Yoon SS3, Beksac M4, Dimopoulos MA5, Elghandour A6, Jedrzejczak WW7, Günther A8, Nakorn TN9, Siritanaratkul N10, Corradini P11, Chuncharunee S12, Lee JJ13, Schlossman RL14, Shelekhova T15, Yong K16, Tan D17, Numbenjapon T18, Cavenagh JD19, Hou J20, LeBlanc R21, Nahi H22, Qiu L23, Salwender H24, Pulini S25, Moreau P26, Warzocha K27, White D28, Bladé J29, Chen W30, de la Rubia J31, Gimsing P32, Lonial S33, Kaufman JL33, Ocio EM34, Veskovski L35, Sohn SK36, Wang MC37, Lee JH38, Einsele H39, Sopala M40, Corrado C40, Bengoudifa BR40, Binlich F41, Richardson PG14. Lancet Oncol. 2014 Oct;15(11):1195-206. doi: 10.1016/S1470-2045(14)70440-1. Epub 2014 Sep 18.
        BACKGROUND: Panobinostat is a potent oral pan-deacetylase inhibitor that in preclinical studies has synergistic anti-myeloma activity when combined with bortezomib and dexamethasone. We aimed to compare panobinostat, bortezomib, and dexamethasone with placebo, bortezomib, and dexamethasone in patients with relapsed or relapsed and refractory multiple myeloma.
        3.HPLC-UV-MS profiles of phenolic compounds and antioxidant activity of fruits from three citrus species consumed in Northern Chile.
        Brito A1, Ramirez JE2, Areche C3, Sepúlveda B4, Simirgiotis MJ5. Molecules. 2014 Oct 29;19(11):17400-21. doi: 10.3390/molecules191117400.
        Peels and edible pulp from three species of citrus including Citrus aurantifolia (varieties pica and sutil) and Citrus x lemon var. Genova widely cultivated and consumed in Northern Chile (I and II region) were analyzed for phenolic compounds and antioxidant activity for the first time. A high performance electrospray ionization mass spectrometry (HPLC-UV-ESI-MS) method was developed for the rapid identification of phenolics in extracts from peels and juices of all species. Several flavonoids including one kaempferol-O-hexoside (peak 16) and one hesperidin derivative (peak 22) three quercetin derivatives (peaks 4, 19 and 36), five isorhamnetin derivatives (peaks 5, 23, 24, 26 and 29) four luteolin derivatives (peaks 14, 25, 27 and 40), seven apigenin derivatives (peaks 2, 3, 12, 20, 34, 35 and 39), seven diosmetin derivatives (peaks 7-9, 17, 21, 31 and 37), three chrysoeriol derivatives (peaks 10, 18 and 30), and four eryodictiol derivatives (peaks 6, 13, 15 and 38) were identified in negative and positive mode using full scan mass measurements and MSn fragmentations.
Bio Calculators
Stock concentration: *
Desired final volume: *
Desired concentration: *

L

* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
g/mol
g
Related Products
BOC Sciences Support

Please contact us with any specific requirements and we will get back to you as soon as possible.


  • Verification code

We invite you to contact us at or through our contact form above for more information about our services and products.

USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Inquiry Basket