447218
硼酸三甲酯
99.999% (trace metal basis)
别名:
三甲氧基硼烷, 硼酸甲酯
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关于此项目
线性分子式:
B(OCH3)3
化学文摘社编号:
分子量:
103.91
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-468-9
Beilstein/REAXYS Number:
1697939
MDL number:
产品名称
硼酸三甲酯, 99.999% (trace metal basis)
InChI key
WRECIMRULFAWHA-UHFFFAOYSA-N
InChI
1S/C3H9BO3/c1-5-4(6-2)7-3/h1-3H3
SMILES string
COB(OC)OC
vapor density
3.59 (vs air)
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.)
Quality Level
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Packaging
建议将 25 mL Sure/密封™瓶作为一次性使用瓶。重复穿刺可能导致产品性能下降。
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
存储类别
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
法规信息
危险化学品
此项目有
A Colorado et al.
Journal of mass spectrometry : JMS, 31(4), 403-410 (1996-04-01)
Barbiturates are a class of drugs that are utilized as anesthetics and sleeping agents and are used for the treatment of anxiety, epilepsy and other psychiatric disorders. Because of their pyrimidine structures, barbiturates are highly basic compounds. The evaluation of
Steven C Habicht et al.
Analytical chemistry, 80(9), 3416-3421 (2008-03-28)
A mass spectrometric method has been developed for the identification of the carboxylic acid functional group in analytes evaporated and ionized by electrospray ionization (ESI). This method is based on gas-phase ion-molecule reactions of ammoniated ([M + NH4]+) and sodiated
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.
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
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
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