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P38005

Sigma-Aldrich

1,3,5-Trihydroxybenzene dihydrate

97%

Synonym(s):

Phloroglucinol dihydrate

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About This Item

Linear Formula:
C6H3(OH)3 · 2H2O
CAS Number:
6099-90-7
Molecular Weight:
162.14
Beilstein:
5109263
EC Number:
203-611-2
MDL number:
MFCD00149090
UNSPSC Code:
12352100
PubChem Substance ID:
24898456
NACRES:
NA.22

Assay

97%

form

solid

mp

218-221 °C (A) (lit.)

SMILES string

O.O.Oc1cc(O)cc(O)c1

InChI

1S/C6H6O3.2H2O/c7-4-1-5(8)3-6(9)2-4;;/h1-3,7-9H;2*1H2

InChI key

MPYXTIHPALVENR-UHFFFAOYSA-N

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Application

In microscopy as a decalcifier of bone specimens. Reagent for pentoses, pentosans and aldehydes.

Hazard Statements

H412

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Margaret Murray et al.
Antioxidants (Basel, Switzerland), 8(2) (2019-03-01)
When healthy adults consume carbohydrates at night, postprandial blood glucose responses are elevated and prolonged compared to daytime.Extended postprandial hyperglycaemia is a risk factor for type 2 diabetes. Polyphenols are bioactive secondary metabolites of plants and algae with potential to
Margaret Murray et al.
Nutrients, 10(3) (2018-03-03)
This study investigated the impact of a polyphenol-rich seaweed extract on postprandial glycaemia in healthy adults, and, as a secondary outcome, the influence of ethnicity on these outcomes. Thirty-eight volunteers (26 non-Asian, 12 Asian) aged 19 to 56 years participated
Yan Wang et al.
Journal of separation science, 42(7), 1332-1340 (2019-01-23)
Three monomers, octakis (3-mercaptopropyl) octasilsesquioxane, 1,2,4-trivinylcyclohexane and isophytol were employed to synthesize a novel monolithic stationary phase via photo-initiated thiol-ene click polymerization for reversed-phase liquid chromatography. Several factors such as porogenic system, reaction time and the molar ratio of functional

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