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Z548960

Sigma-Aldrich

Aldrich® splash protector

female joint: ST/NS 24/40, male joint: ST/NS 14/20

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0.2 MG
CA$741.00
1 MG
CA$1,470.00

About This Item

UNSPSC Code:
41121815
NACRES:
NB.35

CA$741.00

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Joint

female joint: ST/NS24/40
male joint: ST/NS14/20

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This Item
Z548979Z548987Z243892
Aldrich® splash protector female joint: ST/NS 24/40, male joint: ST/NS 14/20

Z548960

Aldrich® splash protector

Aldrich® splash protector female joint: ST/NS 29/32, male joint: ST/NS 14/20

Z548979

Aldrich® splash protector

Aldrich® splash protector female joint: ST/NS 29/32, male joint: ST/NS 24/40

Z548987

Aldrich® splash protector

Aldrich® splash protector female joint: ST/NS 24/40, male joint: ST/NS 24/40

Z243892

Aldrich® splash protector

joint

female joint: ST/NS24/40, male joint: ST/NS14/20

joint

female joint: ST/NS29/32, male joint: ST/NS14/20

joint

female joint: ST/NS29/32, male joint: ST/NS24/40

joint

female joint: ST/NS24/40

General description

Effectively prevents upward movement of foaming or bumping liquids in rotary evaporator traps. Unique design has two baffles with horizontally opposing holes that may also be used with other distillation techniques.

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Aldrich is a registered trademark of Sigma-Aldrich Co. LLC

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Natalya V Belova et al.
The journal of physical chemistry. A, 112(14), 3209-3214 (2008-03-07)
The tautomeric properties of alpha-chlorinated acetylacetone, 3-chloro-2,4-pentanedione CH3C(O)-CHCl-C(O)CH3, have been investigated by gas electron diffraction (GED) and quantum chemical calculations (B3LYP and MP2 approximations with different basis sets up to cc-pVTZ). Analysis of the GED intensities resulted in the presence
Julien Massue et al.
Inorganic chemistry, 44(24), 8740-8748 (2005-11-22)
The reaction of tris(alkylthio)tetrathiafulvalene thiolates with 3-chloro-2,4-pentanedione affords tetrathiafulvalene (TTF) moieties substituted by the acetylacetone function (TTFSacacH), precursors of novel redox-active ligands: the acetylacetonate ions (TTFSacac). These TTFSacacHs have been characterized by X-ray diffraction analyses, and similar trends have been
Almeqdad Y Habashneh et al.
Archiv der Pharmazie, 347(6), 415-422 (2014-03-13)
A new series of N1-(flavon-6-yl)amidrazones were synthesized by reacting the hydrazonoyl chloride derived from 6-aminoflavone with the appropriate sec-cyclic amines. The antitumor activities of these compounds were evaluated on breast cancer (MCF-7) and leukemic (K562) cell lines. Among the compounds
Jennifer A Jacobsen et al.
Journal of medicinal chemistry, 54(2), 591-602 (2010-12-30)
Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced hit rates ranging from 29% to 43% for five matrix metalloproteases

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