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Merck
CN

393657

2-Hydroxymethyl-1,3-propanediol

97%

Synonym(s):

Trimethylolmethane, Tris(hydroxymethyl)methane

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About This Item

Linear Formula:
HC(CH2OH)3
CAS Number:
Molecular Weight:
106.12
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
225-187-8
Beilstein/REAXYS Number:
1733340
MDL number:
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Product Name

2-Hydroxymethyl-1,3-propanediol, 97%

InChI key

SFRDXVJWXWOTEW-UHFFFAOYSA-N

InChI

1S/C4H10O3/c5-1-4(2-6)3-7/h4-7H,1-3H2

SMILES string

OCC(CO)CO

assay

97%

form

solid

mp

63-68 °C (dec.) (lit.)

Quality Level

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Storage Class

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)

Regulatory Information

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Libia Alejandra García-Flores et al.
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Protein kinase C (PKC) and aldose reductase (AR) enzyme activities are increased in diabetes and complications are include retinopathy, nephropathy, and neuropathy. However, the relationship between PKC and AR and the underlying molecular mechanisms is still unclear. We aimed to
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
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

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