393657
2-羟甲基-1,3-丙二醇
97%
别名:
Trimethylolmethane, Tris(hydroxymethyl)methane
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关于此项目
线性分子式:
HC(CH2OH)3
化学文摘社编号:
分子量:
106.12
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
225-187-8
Beilstein/REAXYS Number:
1733340
MDL number:
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
192.2 °F - closed cup
flash_point_c
89 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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Sirun Özçelik et al.
Journal of separation science, 43(7), 1365-1371 (2020-01-21)
Ethylmalonic acid is a metabolic organic acid, and its accumulation in urine is diagnostic of ethylmalonic aciduria. In this study, a simple and fast method employing capillary electrophoresis equipped with capacitively coupled contactless conductivity detection was developed for the detection
Raúl Domínguez-Perles et al.
Food research international (Ottawa, Ont.), 107, 619-628 (2018-03-28)
Phytoprostanes (PhytoPs) and phytofurans (PhytoFs) are prostaglandin-like compounds, contributing to defense signaling and prevention of cellular damage. These plant oxylipins result from autoxidation of α-linolenic acid (ALA) and have been proposed as new bioactive compounds due to their structural analogies
Umar T Twahir et al.
Biochemistry, 55(47), 6505-6516 (2016-11-01)
This contribution describes electron paramagnetic resonance (EPR) experiments on Mn(III) in oxalate decarboxylase of Bacillus subtilis, an interesting enzyme that catalyzes the redox-neutral dissociation of oxalate into formate and carbon dioxide. Chemical redox cycling provides strong evidence that both Mn
Katarina Marković et al.
Molecules (Basel, Switzerland), 25(7) (2020-04-01)
The development of ruthenium-based complexes for cancer treatment requires a variety of pharmacological studies, one of them being a drug's binding kinetics to serum proteins. In this work, speciation analysis was used to study kinetics of ruthenium-based drug candidates with
Raja Chinnappan et al.
Mikrochimica acta, 186(7), 406-406 (2019-06-12)
Okadaic acid (OKA), a marine toxin produced by dinoflagellates, is responsible for most human diarrhetic shellfish poisoning-associated health disorders. A competitive displacement assay for OKA is described here. An OKA-binding aptamer was truncated with two sequences, one labeled with 6-carboxyfluorescein
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