447218
Trimethyl borate
99.999% (trace metal basis)
Synonyme(s) :
Boric acid trimethyl ester, Methyl borate
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A propos de cet article
Formule linéaire :
B(OCH3)3
Numéro CAS:
Poids moléculaire :
103.91
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-468-9
Beilstein/REAXYS Number:
1697939
MDL number:
Assay:
99.999% (trace metal basis)
Service technique
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3.59 (vs air)
Quality Level
assay
99.999% (trace metal basis)
refractive index
n20/D 1.346 (lit.)
bp
68-69 °C (lit.)
mp
−34 °C (lit.)
density
0.932 g/mL at 20 °C (lit.)
SMILES string
COB(OC)OC
InChI
1S/C3H9BO3/c1-5-4(6-2)7-3/h1-3H3
InChI key
WRECIMRULFAWHA-UHFFFAOYSA-N
Packaging
The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 1B - STOT SE 1
target_organs
Eyes
Classe de stockage
3 - Flammable liquids
wgk
WGK 1
flash_point_f
12.2 °F - (own results)
flash_point_c
-11 °C - (own results)
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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R Meder et al.
Solid state nuclear magnetic resonance, 15(1), 69-72 (2000-07-21)
Boron-11 nuclear magnetic resonance imaging and spectroscopy have been used to characterise the nature and distribution of boron compounds after preservative treatment of radiata pine wood with trimethylborate (TMB). One day after treatment, 11B magnetic resonance imaging microscopy showed significant
Scott Gronert et al.
Journal of the American Society for Mass Spectrometry, 13(9), 1088-1098 (2002-09-27)
Using a quadrupole ion trap mass spectrometer, trimethyl borate was allowed to react with dihydrogen phosphate, deprotonated O-phosphoserine, and a set of hydrogen bonded complexes involving dihydrogen phosphate and neutral acids (phosphoric acid, acetic acid, serine, and O-phosphoserine). The reactions
Jayalakshmi Somuramasami et al.
Journal of the American Society for Mass Spectrometry, 22(6), 1040-1051 (2011-09-29)
Several lignin model compounds were examined to test whether gas-phase ion-molecule reactions of trimethylborate (TMB) in a FTICR can be used to differentiate the ortho-, meta-, and para-isomers of protonated aromatic compounds, such as those formed during degradation of lignin.