Skip to Content
Merck
CN

95193

Cap A (acetic anhydride 10% in THF/lutidine 8 : 1)

suitable for DNA synthesis

Synonym(s):

Acetic anhydride solution

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

CAS Number:
UNSPSC Code:
12352200
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

SMILES string

CC(=O)OC(C)=O

technique(s)

DNA synthesis: suitable

impurities

≤0.005% water

density

0.911 g/mL at 20 °C

Application

Reagent used in the phosphite triester method of oligonucleotide synthesis for the capping of the remaining free 5′-hydroxyl groups by acetylation. Reagent is suitable for use on ABI, Beckman synthesizers.

Preparation Note

filtered with a 0.1 μm filter

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

1.4 °F - closed cup

flash_point_c

-17.0 °C - closed cup

ppe

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

Regulatory Information

危险化学品
易制毒化学品(2类)
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

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

Visit the Document Library

Chunyan Hu et al.
Journal of agricultural and food chemistry, 59(19), 10517-10523 (2011-09-03)
Poultry feathers are renewable resources, inexpensive and abundantly available, but have limited applications. Although keratin extracted from feathers has been chemically modified, there are no reports on the chemical modification or development of thermoplastics from poultry feathers. Acetylation is an
Manuel Weber et al.
The Journal of organic chemistry, 77(23), 10846-10855 (2012-12-01)
A multicomponent reaction is reported generating highly enantioenriched and diastereomerically pure quaternary amino acid derivatives via 1,4-addition of azlactones to enones. The azlactone intermediates are generated in situ from unprotected α-amino acids and acetic anhydride. Previous attempts using bis-palladacycle catalysts
In-Taek Hwang et al.
Molecules (Basel, Switzerland), 16(8), 6313-6321 (2011-07-28)
An efficient synthesis of 4-arylcoumarins has been accomplished via Kostanecki reactions of 2-hydroxybenzophenones with acetic anhydride employing DBU at ambient temperature. Using the same strategy, several 2-acyloxybenzophenone derivatives were readily converted to 3,4-difunctionalized coumarins. This protocol offers a notable improvement
Rie Ito et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(31), 3714-3720 (2011-11-01)
A simple, rapid and sensitive method termed dispersive liquid-liquid microextraction (DLLME) combined with gas chromatography-mass spectrometry (GC/MS) was developed for the determination of tricyclic antidepressants (TCAs) in human urine sample. An appropriate mixture of methanol (disperser solvent), carbon tetrachloride (extraction
V Chiaradia et al.
Applied biochemistry and biotechnology, 168(4), 742-751 (2012-08-07)
Enzymatic esterification of eugenol is a matter of great scientific and technological interest due to the well-known drawbacks of the chemical-catalyzed route as well as the potential use of produced compounds as natural antimicrobials. This work reports the maximization of

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