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447218

Sigma-Aldrich

Trimethyl borate

99.999% (trace metal basis)

Sinonimo/i:

Boric acid trimethyl ester, Methyl borate

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About This Item

Formula condensata:
B(OCH3)3
Numero CAS:
121-43-7
Peso molecolare:
103.91
Beilstein:
1697939
Numero CE:
204-468-9
Numero MDL:
MFCD00008346
Codice UNSPSC:
12352103
ID PubChem:
24868324
NACRES:
NA.22

Densità del vapore

3.59 (vs air)

Saggio

99.999% (trace metal basis)

Indice di rifrazione

n20/D 1.346 (lit.)

P. eboll.

68-69 °C (lit.)

Punto di fusione

−34 °C (lit.)

Densità

0.932 g/mL at 20 °C (lit.)

Stringa SMILE

COB(OC)OC

InChI

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

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Confezionamento

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

Note legali

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

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Eyes

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

12.2 °F - (own results)

Punto d’infiammabilità (°C)

-11 °C - (own results)

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
SHBN4854
SHBM4476
SHBL9314
SHBJ5140
SHBD9104V

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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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