CAS Number2922-28-3
Synonyms6-Aminopurine hydrochloride hydrate; 7H-Purin-6-amine hydrochloride; 7H-Purin-6-amine hydrochloride (1:1); MFCD00075782; Adenine monohydrochloride; 7H-Purin-6-amine, hydrochloride (1:1); Adenine hydrochloride; 6-Aminopurine Hydrochloride Hemihydrate; EINECS 220-867-0
Molecular FormulaC5H6ClN5
Molecular Weight171.59
Purity≥99.0 (HPLC)%
Boiling Point553.5ºC at 760 mmHg
Melting Point~285 °C (dec.)
AppearanceWhite to light yellow crystal powder
EINECS220-867-0
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 2922-28-3 |
| Catalog No. | 2A-9007071 |
| Chinese Name | 腺嘌呤盐酸盐半水合物 |
| Synonyms | 6-Aminopurine hydrochloride hydrate; 7H-Purin-6-amine hydrochloride; 7H-Purin-6-amine hydrochloride (1:1); MFCD00075782; Adenine monohydrochloride; 7H-Purin-6-amine, hydrochloride (1:1); Adenine hydrochloride; 6-Aminopurine Hydrochloride Hemihydrate; EINECS 220-867-0 |
| Molecular Formula | C5H6ClN5 |
| Molecular Weight | 171.59 |
| Purity | ≥99.0 (HPLC) |
| Boiling Point | 553.5ºC at 760 mmHg |
| Melting Point | ~285 °C (dec.) |
| Appearance | White to light yellow crystal powder |
| Water Solubility | H2O: 50 mg/mL |
| Storage Condition | Sealed in a cool, dry environment |
| Application | Adenine hydrochloride (6-Aminopurine hydrochloride) is a purine derivative that plays a variety of roles in biochemistry, including cellular respiration, formation of high-energy ATP and coenzyme fact |
| EINECS | 220-867-0 |
| HTC | 2933990090 |
| PubChem ID | 329747363 |
| MDL Number | MFCD00075782 |
| SMILES | Cl[H].Nc1ncnc2[nH]cnc12 |
| InChI | 1S/C5H5N5.ClH/c6-4-3-5(9-1-7-3)10-2-8-4;/h1-2H,(H3,6,7,8,9,10);1H |
| InChI Key | UQVDQSWZQXDUJB-UHFFFAOYSA-N |
| Beilstein/REAXYS | 4009585 |
| NACRES Code | NA.22 |
| UNSPSC | 12352100 |
| Hazard Symbols | Transport |
| Risk Codes | R22 |
| MSDS | msds/7071_1_2922_28_3.pdf |
| Bioactivity | Adenine hydrochloride (6-Aminopurine hydrochloride) is a purine derivative with a variety of roles in biochemistry, including cellular respiration, in the form of both the energy-rich adenosine triphosphate (ATP) and the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD), and protein synthesis, as a chemical component of DNA and RNA[1][2]. Related Catalog Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis Target Target: Human Endogenous Metabolite References [1]. Reader V. The assay of vitamin B(4). Biochem J. 1930;24(6):1827-31. [2]. ORO J, et al. Synthesis of purines under possible primitive earth conditions. I. Adenine from hydrogen cyanide. Arch Biochem Biophys. 1961 Aug;94:217-27. Chemical & Physical Properties Boiling Point 553.5ºC at 760 mmHg Melting Point ~285 °C (dec.) Molecular Formula C5H6ClN5 Molecular Weight 171.588 Flash Point 322.7ºC Exact Mass 171.031174 PSA 80.48000 LogP 1.31830 InChIKey UQVDQSWZQXDUJB-UHFFFAOYSA-N SMILES Cl.Nc1ncnc2nc[nH]c12 Water Solubility H2O: 50 mg/mL |
| Use of | Adenine hydrochloride (6-Aminopurine hydrochloride) is a purine derivative with a variety of roles in biochemistry, including cellular respiration, in the form of both the energy-rich adenosine triphosphate (ATP) and the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD), and protein synthesis, as a chemical component of DNA and RNA[1][2]. Properties Name Adenine hydrochloride hydrate Synonym More Synonyms Adenine hydrochloride Biological Activity Description Adenine hydrochloride (6-Aminopurine hydrochloride) is a purine derivative with a variety of roles in biochemistry, including cellular respiration, in the form of both the energy-rich adenosine triphosphate (ATP) and the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD), and protein synthesis, as a chemical component of DNA and RNA[1][2]. Related Catalog Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis Target: Human Endogenous Metabolite References [1]. Reader V. The assay of vitamin B(4). Biochem J. 1930;24(6):1827-31. [2]. ORO J, et al. Synthesis of purines under possible primitive earth conditions. I. Adenine from hydrogen cyanide. Arch Biochem Biophys. 1961 Aug;94:217-27. Chemical & Physical Properties Exact Mass 171.031174 PSA 80.48000 LogP 1.31830 InChIKey UQVDQSWZQXDUJB-UHFFFAOYSA-N SMILES Cl.Nc1ncnc2nc[nH]c12 |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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