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SU860114

Supelco

Snap Ring polypropylene autosampler microvial

volume 0.3 mL

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100 μL
CA$531.00

CA$531.00

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100 μL
CA$531.00

About This Item

UNSPSC Code:
41122001
NACRES:
NB.11

CA$531.00

Please contact Customer Service for Availability
Request a Bulk Order
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material

clear polypropylene (with integrated 0.3 mL polypropylene insert)

packaging

pkg of 1000 ea

availability

not available in USA

O.D.

11.6 mm

diam. × H × I.D.

11.6 m × 32 mm × 6.0 mm

volume

0.3 mL

fitting

thread for 11 mm

compatibility

11 mm crimp cap or 11 mm snap top seal
for use with 11 mm snap caps or crimp seals

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    Determination of the hydrogenation degree of telechelic polybutadiene by 1HNMR
    Lira CH, et al.
    Magnetic Resonance in Chemistry, 5, 22-22 (2006)
    Triphenylcarbenium Tetrafluoroborate as an Efficient Catalyst in the Regioselective Reductive Ring Opening of Benzylidene Acetals of Carbohydrates
    Thota N, et al.
    ChemistrySelect, 4(27), 7976-7980 (2019)
    Synthesis and transannular Diels-Alder reaction of a cis-trans-trans and a trans-cis-cis 13-membered macrocyclic trienone
    Marinier A, et al.
    Canadian Journal of Chemistry, 67(10), 1609-1617 (1989)
    Damien Webb et al.
    Organic letters, 14(2), 568-571 (2011-12-31)
    A continuous flow system for the multiparameter (flow rate, temperature, residence time, stoichiometry) optimization of the DIBALH reduction of esters to aldehydes is described. Incorporating an in-line quench (MeOH), these transformations are generally complete in fewer than 60 s. Mixing
    Hidetsura Cho et al.
    The Journal of organic chemistry, 75(3), 627-636 (2009-12-31)
    A systematic investigation of the reductive ring-expansion reaction of cyclic ketoximes fused to aromatic rings with diisobutylaluminum hydride (DIBALH) is described. This reaction regioselectively afforded a variety of five- to eight-membered bicyclic heterocycles or tricyclic heterocycles containing nitrogen neighboring an
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