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Merck
CN

92330

Sigma-Aldrich

硼酸三甲酯

purum, ≥99.0% (GC)

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
Beilstein:
1697939
EC 号:
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽密度

3.59 (vs air)

质量水平

等级

purum

方案

≥99.0% (GC)

表单

liquid

折射率

n20/D 1.346 (lit.)
n20/D 1.358

沸点

68-69 °C (lit.)

mp

−34 °C (lit.)

密度

0.932 g/mL at 20 °C (lit.)

SMILES字符串

COB(OC)OC

InChI

1S/C3H9BO3/c1-5-4(6-2)7-3/h1-3H3

InChI key

WRECIMRULFAWHA-UHFFFAOYSA-N

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应用

硼酸三甲酯(TMB)可用于:
  • 合成以三苯胺为核、外围接四苯乙烯单元的发光分子。
  • 合成硼烷氨和三烷基胺硼烷。
  • 在硼烷二甲硫醚的存在下还原羧酸。
  • 交联磷酸盐复合物。
  • 作为化学气相沉积法合成氮化硼纳米管的硼源。

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 1B - STOT SE 1

靶器官

Eyes

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

12.2 °F - (own results)

闪点(°C)

-11 °C - (own results)

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Organic synthesis using borane-methyl sulfide. II. Reduction of aromatic carboxylic acids in the presence of trimethyl borate.
Lane CF, et al.
The Journal of Organic Chemistry, 39(20), 3052-3054 (1974)
Thermal-heating CVD synthesis of BN nanotubes from trimethyl borate and nitrogen gas.
Lin FH, et al.
Materials Chemistry and Physics, 107(1), 115-121 (2008)
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.
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

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