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Key Documents

B6768

Sigma-Aldrich

Acide borique

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

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About This Item

Formule linéaire :
H3BO3
Numéro CAS:
Poids moléculaire :
61.83
Numéro CE :
Numéro MDL:
Code UNSPSC :
12161700
eCl@ss :
38120104
ID de substance PubChem :
Nomenclature NACRES :
NA.25

Qualité

for molecular biology

Niveau de qualité

Pression de vapeur

2.6 mmHg ( 20 °C)

Gamme de produits

BioReagent

Pureté

≥99.5%

Forme

powder

Technique(s)

cell culture | mammalian: suitable
cell culture | plant: suitable

pH

5.1 (25 °C, 1.8 g/L)

Pf

160 °C (dec.) (lit.)

Solubilité

water: 40 mg/mL, clear, colorless

Densité

1.49 g/cm3 at 23 °C

Traces de cations

Fe: ≤5 ppm
Mg: ≤5 ppm
heavy metals (as Pb): ≤10 ppm

Absorption UV

λ: 260 nm Amax: 0.05
λ: 280 nm Amax: 0.05

Activité étrangère

DNase, RNase, and protease, none detected

Température de stockage

room temp

Chaîne SMILES 

OB(O)O

InChI

1S/BH3O3/c2-1(3)4/h2-4H

Clé InChI

KGBXLFKZBHKPEV-UHFFFAOYSA-N

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Description générale

Boric acid is a weak monobasic Lewis acid (electron pair acceptor), which reacts reversibly with alcohols. It is used in dermal and women′s hygiene products due to its mild antibacterial and antifungal effects. Boric acid is used as a buffer in ophthalmic products. It acts as an effective solid lubrication agent because of its molecular structure. Boric acid finds its applications in glass making, fire retardant. Boric acid is used in biochemistry in buffer solutions. It also forms complex equilibria in solution, with the tetraborate ion (B4O7 2- ) being the predominant species. Borate buffers are involved in discontinuous electrophoresis and capillary electrophoresis systems for the separation of proteins and nucleic acids.

Application

Boric acid has been used:
  • to prepare boric buffer for the quantification of primary amine groups at the surface of nanocapsules
  • to study its effects on epigenetic change
  • for the estimation of protein in wheatgrass using Kjeldahl method

Used to promote amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents.
Intensified Azeotropic Distillation: A Strategy for Optimizing Direct Amidation

Caractéristiques et avantages

  • Environment-friendly
  • Non-toxic 

Pictogrammes

Health hazard

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Repr. 1B

Code de la classe de stockage

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


Certificats d'analyse (COA)

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