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Merck
CN

CDS000626

Sodium hydroxyacetate

AldrichCPR

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经验公式(希尔记法):
C2H3NaO3
化学文摘社编号:
分子量:
98.03
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
220-624-9
MDL number:
NACRES:
NA.21
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产品名称

Sodium hydroxyacetate, AldrichCPR

InChI key

VILMUCRZVVVJCA-UHFFFAOYSA-M

InChI

1S/C2H4O3.Na/c3-1-2(4)5;/h3H,1H2,(H,4,5);/q;+1/p-1

SMILES string

[Na+].OCC([O-])=O

form

solid

Other Notes

Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.

NOTWITHSTANDING ANY CONTRARY PROVISION CONTAINED IN SIGMA-ALDRICH′S STANDARD TERMS AND CONDITIONS OF SALE OR AN AGREEMENT BETWEEN SIGMA-ALDRICH AND BUYER, SIGMA-ALDRICH SELLS THIS PRODUCT "AS-IS" AND MAKES NO REPRESENTATION OR WARRANTY WHATSOEVER WITH RESPECT TO THIS PRODUCT, INCLUDING ANY (A) WARRANTY OF MERCHANTABILITY; (B) WARRANTY OF FITNESS FOR A PARTICULAR PURPOSE; OR (C) WARRANTY AGAINST INFRINGEMENT OF INTELLECTUAL PROPERTY RIGHTS OF A THIRD PARTY; WHETHER ARISING BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE.

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

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Wun Chyi Chin et al.
Pharmaceutical development and technology, 21(2), 222-230 (2014-12-19)
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H Rajpurohit et al.
Journal of young pharmacists : JYP, 3(3), 211-215 (2011-09-08)
In the present study, fast disintegrating tablets were designed with a view to enhance patient compliance. In this method, the hull of Hordeum vulgare, cross carmellose sodium, and sodium starch glycolate were used as superdisintegrants (4 and 6%), along with
Jeong S Kim et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 82, 45-51 (2015-11-26)
The oral bioavailability (BA) of risedronate sodium (RS), an antiresorptive agent, is less than 1% due to its low membrane permeability as well as the formation of non-absorbable complexes with multivalent cations such as calcium ion (Ca(2+)) in the gastrointestinal
R C Doijad et al.
Indian journal of pharmaceutical sciences, 70(2), 203-207 (2008-03-01)
The present study is aimed at the overall improvement in the efficacy, reduced toxicity and enhancement of therapeutic index of cisplatin. Solid lipid nanoparticulate delivery system of cisplatin has been developed by microemulsification method by using stearic acid, soy lecithin
D M Patel et al.
Indian journal of pharmaceutical sciences, 70(1), 71-76 (2008-01-01)
The purpose of this investigation was to develop fast dissolving tablets of etoricoxib. Granules containing etoricoxib, menthol, crospovidone, aspartame and mannitol were prepared by wet granulation technique. Menthol was sublimed from the granules by exposing the granules to vacuum. The

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