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2,2-Bis(hydroxymethyl)butyric acid

CAS# 10097-02-6

2,2-Bis(hydroxymethyl)butyric acid

Catalog No. BCC8495----Order now to get a substantial discount!

Product Name & Size Price Stock
2,2-Bis(hydroxymethyl)butyric acid:5mg Please Inquire In Stock
2,2-Bis(hydroxymethyl)butyric acid:10mg Please Inquire In Stock
2,2-Bis(hydroxymethyl)butyric acid:20mg Please Inquire In Stock
2,2-Bis(hydroxymethyl)butyric acid:50mg Please Inquire In Stock

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Chemical structure

2,2-Bis(hydroxymethyl)butyric acid

3D structure

Chemical Properties of 2,2-Bis(hydroxymethyl)butyric acid

Cas No. 10097-02-6 SDF Download SDF
PubChem ID 3301396 Appearance Powder
Formula C6H12O4 M.Wt 148
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2,2-bis(hydroxymethyl)butanoic acid
SMILES CCC(CO)(CO)C(=O)O
Standard InChIKey JVYDLYGCSIHCMR-UHFFFAOYSA-N
Standard InChI InChI=1S/C6H12O4/c1-2-6(3-7,4-8)5(9)10/h7-8H,2-4H2,1H3,(H,9,10)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

2,2-Bis(hydroxymethyl)butyric acid Dilution Calculator

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2,2-Bis(hydroxymethyl)butyric acid Molarity Calculator

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Preparing Stock Solutions of 2,2-Bis(hydroxymethyl)butyric acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.7568 mL 33.7838 mL 67.5676 mL 135.1351 mL 168.9189 mL
5 mM 1.3514 mL 6.7568 mL 13.5135 mL 27.027 mL 33.7838 mL
10 mM 0.6757 mL 3.3784 mL 6.7568 mL 13.5135 mL 16.8919 mL
50 mM 0.1351 mL 0.6757 mL 1.3514 mL 2.7027 mL 3.3784 mL
100 mM 0.0676 mL 0.3378 mL 0.6757 mL 1.3514 mL 1.6892 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 2,2-Bis(hydroxymethyl)butyric acid

Selective oxidation of trimethylolpropane to 2,2-bis(hydroxymethyl)butyric acid using growing cells of Corynebacterium sp. ATCC 21245.[Pubmed:26804932]

J Biotechnol. 2016 Mar 10;221:62-9.

Multifunctional chemicals including hydroxycarboxylic acids are gaining increasing interest due to their growing applications in the polymer industry. One approach for their production is a biological selective oxidation of polyols, which is difficult to achieve by conventional chemical catalysis. In the present study, trimethylolpropane (TMP), a trihydric alcohol, was subjected to selective oxidation using growing cells of Corynebacterium sp. ATCC 21245 as a biocatalyst and yielding the dihydroxy-monocarboxylic acid, 2,2-Bis(hydroxymethyl)butyric acid (BHMB). The study revealed that co-substrates are crucial for this reaction. Among the different evaluated co-substrates, a mixture of glucose, xylose and acetate at a ratio of 5:5:2 was found optimum. The optimal conditions for biotransformation were pH 8, 1v/v/m airflow and 500rpm stirring speed. In batch mode of operation, 70.6% of 5g/l TMP was converted to BHMB in 10 days. For recovery of the product the adsorption pattern of BHMB to the anion exchange resin, Ambersep((R)) 900 (OH(-)), was investigated in batch and column experiments giving maximum static and dynamic binding capacities of 135 and 144mg/g resin, respectively. BHMB was separated with 89.7% of recovery yield from the fermentation broth. The approach is applicable for selective oxidation of other highly branched polyols by biotransformation.

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