316393
Sodium triacetoxyborohydride
97%
Manufacturer: Sigma Aldrich
CAS Number: 56553-60-7
Synonym(S): STAB
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 25 G | 316393-25-G | In Stock | ₹ 3,850.00 |
| 100 G | 316393-100-G | In Stock | ₹ 14,610.00 |
| 500 G | 316393-500-G | In Stock | ₹ 54,698.73 |
| 1 KG | 316393-1-KG | In Stock | ₹ 62,840.00 |
316393 - 25 G
In Stock
Quantity
1
Base Price: ₹ 3,850.00
GST (18%): ₹ 693.00
Total Price: ₹ 4,543.00
Quality Level
200
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
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Sigma Aldrich Fine Chemicals Biosciences Sodium Triacetoxyborohydride | 56553-60-7 | MFCD00012211 | 100g | -- | ₹ 16,979.38 | |
| | Sigma Aldrich Fine Chemicals Biosciences Sodium triacetoxyborohydride 97% | 56553-60-7 | MFCD00012211 | 500G | -- | ₹ 77,537.89 | |
| | eMolecules Sodium triacetoxyborohydride | 56553-60-7 | MFCD00012211 | 100g | -- | ₹ 10,075.55 | |
| | Sodium triacetoxyborohydride | -- | ₹ 19,369.99 - ₹ 35,750.00 | |
| | Sodium Triacetoxyborohydride | -- | ₹ 256.68 - ₹ 66,651.24 | |
| | 56553-60-7 | Sodium triacetoxyborohydride | -- | ₹ 855.60 - ₹ 3,850.20 |
Related Products
Description
- General description: Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] 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.[2][3] To prepare N-benzyl-γ-valerolactam by reacting with methyl 4-oxopentanoate and benzylamine via reductive amination/lactamization.[3] To reduce imines and enamines to corresponding amines.[2] To reduce quinolines and isoquinolines to corresponding tetrahydro derivatives.[2] In the hydroboration of alkenes.[4] To synthesize nitroxide biradicals for creating high relaxivity terminal groups linkage to dendrimers.[5]Applications using Sodium triacetoxyborohydride
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
P210 - P231 + P232 - P280 - P301 + P312 - P305 + P351 + P338 - P308 + P313
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Sol. 1 - Repr. 1B - Water-react 1
Supplementary Hazards
EUH014
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable