Skip to Content
Merck
All Photos(4)

Key Documents

316393

Sigma-Aldrich

Sodium triacetoxyborohydride

97%

Synonym(s):

STAB

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3COO)3BHNa
CAS Number:
Molecular Weight:
211.94
Beilstein:
4047608
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

reaction suitability

reagent type: reductant

mp

116-120 °C (dec.) (lit.)

SMILES string

[Na+].CC(=O)O[BH-](OC(C)=O)OC(C)=O

InChI

1S/C6H10BO6.Na/c1-4(8)11-7(12-5(2)9)13-6(3)10;/h7H,1-3H3;/q-1;+1

InChI key

HHYFEYBWNZJVFQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity. It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.

Application

Sodium triacetoxyborohydride or [NaBH(OAc)3] can be used as a reagent:
  • In the reductive amination of ketones and aldehydes.
  • To prepare N-benzyl-γ-valerolactam by reacting with methyl 4-oxopentanoate and benzylamine via reductive amination/lactamization.
  • To reduce imines and enamines to corresponding amines.
  • To reduce quinolines and isoquinolines to corresponding tetrahydro derivatives.
  • In the hydroboration of alkenes.
  • To synthesize nitroxide biradicals for creating high relaxivity terminal groups linkage to dendrimers.
Applications using Sodium triacetoxyborohydride

related product

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Sol. 1 - Repr. 1B - Water-react 1

Supplementary Hazards

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride
Abdel-Magid AF, Maryanoff CA, Carson KG
Tetrahedron Letters, 31 (39), 5595-5598 (1990)
A review on the use of sodium triacetoxyborohydride in the reductive amination of ketones and aldehydes
Abdel-Magid AF and Mehrman SJ
Organic Process Research & Development, 10(5), 971-1031 (2006)
Use of Sodium Triacetoxyborohydride in Reductive Amination of Ketones and Aldehydes
Abdel-Magid et al.
ACS Symp. Ser., 641, 201-216 (1996)
Methods of enhancement of reactivity and selectivity of sodium borohydride for applications in organic synthesis
Periasamy M and Thirumalaikumar M
Journal of Organometallic Chemistry, 609(1-2), 137-151 (2000)
Use of sodium triacetoxyborohydride in the synthesis of nitroxide biradicals
Rosen GM, et al.
Journal of the Chemical Society. Perkin Transactions 1, 609(23), 2663-2667 (2002)

Articles

Sodium triacetoxyborohydride

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service