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等级
anhydrous
质量水平
Agency
USP/NF
tested according to Ph. Eur.
方案
99.5% dry basis
表单
crystalline
mp
884 °C (lit.)
溶解性
water: soluble 185 g/L
密度
2.68 g/mL at 25 °C (lit.)
SMILES字符串
[Na+].[Na+].[O-]S([O-])(=O)=O
InChI
1S/2Na.H2O4S/c;;1-5(2,3)4/h;;(H2,1,2,3,4)/q2*+1;/p-2
InChI key
PMZURENOXWZQFD-UHFFFAOYSA-L
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储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Teppei Adachi et al.
Inflammatory bowel diseases, 21(1), 31-39 (2014-12-02)
Expression of heat shock protein A4 (HSPA4, also called Apg-2), a member of the HSP110 family, is induced by several forms of stress. The physiological and pathological functions of HSPA4 in the intestine remain to be elucidated. We assessed HSPA4
Erik C Dreaden et al.
ACS nano, 8(8), 8374-8382 (2014-08-08)
Active targeting of nanoscale drug carriers can improve tumor-specific delivery; however, cellular heterogeneity both within and among tumor sites is a fundamental barrier to their success. Here, we describe a tumor microenvironment-responsive layer-by-layer (LbL) polymer drug carrier that actively targets
Thomas Canam et al.
Plant science : an international journal of experimental plant biology, 198, 17-26 (2012-12-04)
Brassica carinata (Ethiopian mustard) has previously been identified as a potential crop species suitable for marginal land in the North American prairies due to its relatively high salt tolerance. Two genetically related B. carinata lines with brown-seeded (BS) and yellow-seeded
Betina Fejerskov et al.
ACS applied materials & interfaces, 4(9), 4981-4990 (2012-09-04)
In this work, we characterize physical hydrogels based on poly(vinyl alcohol), PVA, as intelligent biointerfaces for surface-mediated drug delivery. Specifically, we assemble microstructured (μS) surface adhered hydrogels via noncryogenic gelation of PVA, namely polymer coagulation using sodium sulfate (Na(2)SO(4)). We
Roosmarijn E Vandenbroucke et al.
Nature reviews. Drug discovery, 13(12), 904-927 (2014-11-08)
Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that form a family of 24 members in mammals. Evidence of the pathological roles of MMPs in various diseases, combined with their druggability, has made them attractive therapeutic targets. Initial drug discovery efforts focused
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