2′-Deoxyadenosine-5′-Monophosphate Free Acid (dAMP) CAS 653-63-4 HPLC Purity ≥98.0%
Manufacturer Supply Deoxynucleotide Intermediates with High Purity and Stable Quality
2'-Deoxyadenosine-5'-Monophosphate Disodium Salt (dGMP.Na2) CAS: 33430-61-4
2'-Deoxyadenosine-5'-Monophosphate Free Acid (dAMP) CAS: 653-63-4
2'-Deoxycytidine-5'-Monophosphate Hydrate (dCMP) CAS: 1032-65-1
Chemical Name | 2'-Deoxyadenosine-5'-Monophosphate Free Acid |
Synonyms | dAMP; 5'-dAMP; 2'-Deoxyadenosine 5'-Phosphate |
CAS Number | 653-63-4 |
Stock Status | In Stock |
Molecular Formula | C10H14N5O6P |
Molecular Weight | 331.22 |
Melting Point | 148℃ |
Solubility | Soluble in 1N Ammonium Hydroxide (50 mg/ml) and Water |
COA & MSDS | Available |
Place of Origin | Shanghai, China |
Brand | Ruifu Chemical |
Item | Specifications | Specifications |
Appearance | White Crystalline Powder | White Crystalline Powder |
Transmission | ≥95.0% | 97.2% |
Assay | ≥90.0% (UV Spectrophotom) | 98.5% |
A250/A260 | 0.79~0.85 | 0.82 |
A280/A260 | 0.20~0.26 | 0.24 |
Water Content | ≤10.0% | 5.5% |
Heavy Metals | ≤10ppm | <10ppm |
Arsenic (As) | ≤2ppm | <2ppm |
Purity / Analysis Method | ≥98.0% (HPLC) | 98.6% (HPLC) |
pH Value | 2.0~3.5 | 3.1 |
Test Standard | Enterprise Standard | Conforms |
Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool and dry place; Protect from sunlight, moisture
Risk Codes
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S37/39 - Wear suitable gloves and eye/face protection
S24/25 - Avoid contact with skin and eyes.
WGK Germany 3
HS Code 2934993090
2′-Deoxyadenosine 5′-Monophosphate (CAS 653-63-4) is used to study adenosine-based cellular interactions. 2'-Deoxyadenosine-5'-Monophosphate is a derivative of the nucleic acid, AMP, in which the hydroxyl group on the 2' carbon of the pentose has been reduced to a hydrogen atom. It has been used in the synthesis of novel photoaffinity labels for incorporation into DNA and to study adenosine-based interactions during DNA synthesis and DNA damage.