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447218

Sigma-Aldrich

Trimethyl borate

99.999% (trace metal basis)

Sinônimo(s):

Boric acid trimethyl ester, Methyl borate

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About This Item

Fórmula linear:
B(OCH3)3
Número CAS:
121-43-7
Peso molecular:
103.91
Beilstein:
1697939
Número CE:
204-468-9
Número MDL:
MFCD00008346
Código UNSPSC:
12352103
ID de substância PubChem:
24868324
NACRES:
NA.22

densidade de vapor

3.59 (vs air)

Nível de qualidade

100

Ensaio

99.999% (trace metal basis)

índice de refração

n20/D 1.346 (lit.)

pb

68-69 °C (lit.)

pf

−34 °C (lit.)

densidade

0.932 g/mL at 20 °C (lit.)

cadeia de caracteres SMILES

COB(OC)OC

InChI

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

chave InChI

WRECIMRULFAWHA-UHFFFAOYSA-N

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Categorias relacionadas

Embalagem

The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

Informações legais

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Eyes

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

12.2 °F - (own results)

Ponto de fulgor (°C)

-11 °C - (own results)

Equipamento de proteção individual

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

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Tetraetil ortossilicato 99.999% trace metals basis

Sigma-Aldrich

333859

Tetraetil ortossilicato

Ácido bórico BioReagent, for molecular biology, suitable for cell culture, suitable for plant cell culture, ≥99.5%

Sigma-Aldrich

B6768

Ácido bórico

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
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.
Ryan J Eismin et al.
Journal of the American Society for Mass Spectrometry, 23(1), 12-22 (2011-10-18)
A mass spectrometric method has been delineated for the identification of the epoxide functionalities in unknown monofunctional analytes. This method utilizes gas-phase ion/molecule reactions of protonated analytes with neutral trimethyl borate (TMB) followed by collision-activated dissociation (CAD) in an ion
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