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Deoxyribonucleic Acid

HCID 44135672
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Grundinformationen

CAS
9007-49-2
Standard-SMILES
NC1CC(O)C(COP(=O)(O)OC2CC(N)OC2COP(=O)(O)OC2CC(N)OC2CO)O1
InChIKey
AWBASQCACWFTGD-UHFFFAOYSA-N
Summenformel
C15H31N3O13P2
Durchschnittliche Molmasse
523,3665 g/mol

Namen und Bezeichner

Bevorzugter Name
Deoxyribonucleic Acid
Englischer Name
Deoxyribonucleic Acid
Summenformel
C15H31N3O13P2
Molmasse
523.366462

Namen und Synonyme

DNAPolydeoxyribonucleotidePolynucleotideDnanPUC19PUC18DNAsoduimPTZ 18U PLASMID DNAhpDNAC00039

Datenbank-Bezeichner

CAS
9007-49-2
PubChem CID
44135672
EC Number
805-335-3

Eigenschaften

Physikochemische Eigenschaften

Dichte
1 g/mL · 1.00 g/mL at 20 °C
storage temp.
-20 °C · -20°C
Löslichkeit
50 mM · 50 mM Tris pH 8.0: 10 mg/mL, clear, faintly brown-yellow
Aggregatzustand
buffered aqueous solution
Farbe
White to Light yellow to Light orange
Biologische Quelle
human placenta
Wasserlöslichkeit
2 mg/ml · Dissolve in TE buffer or water at 2mg/ml
Kosmetik-Inhaltsstoffe Funktionen
SKIN CONDITIONING
InChI
1S/C15H31N3O13P2/c16-13-1-7(20)11(28-13)5-25-32(21,22)31-9-3-15(18)29-12(9)6-26-33(23,24)30-8-2-14(17)27-10(8)4-19/h7-15,19-20H,1-6,16-18H2,(H,21,22)(H,23,24)
InChIKey
AWBASQCACWFTGD-UHFFFAOYSA-N
SMILES
[P](=O)(OC2C(OC(C2)N)CO[P](=O)(OC3C(OC(C3)N)CO)O)(OCC1OC(CC1O)N)O

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

F
3-10-21
wgk
3
tsca
Yes
hs_code
29349990
RTECS-Nr.
HG1933000
hazard_code
B
safety_code
22-24/25
Speicherklasse
11 - Combustible Solids

Chemie und Industrie

Anwendungen · 3 Einträge

BeschreibungDeoxyribonucleic acid (abbreviated DNA) is the molecule that carries genetic information for the development and functioning of an organism. DNA is made of two linked strands that wind around each other to resemble a twisted ladder — a shape known as a double helix. Each strand has a backbone of alternating sugar (deoxyribose) and phosphate groups. Attached to each sugar is one of four bases: adenine (A), cytosine (C), guanine (G), or thymine (T). The two strands are connected by chemical bonds between the bases: adenine bonds with thymine, and cytosine bonds with guanine. The sequence of the bases along DNA’s backbone encodes biological information, such as the instructions for making a protein or RNA molecule.

HistoryDeoxyribonucleic Acid (DNA) was first recognized and identified by the Swiss biologist Johannes Friedrich Miescher in 1869 during his research on white blood cells. The double helix structure of a DNA molecule was later discovered through experimental data by James Watson and Francis Crick. Finally, it was proved that DNA is responsible for storing genetic information in living organisms.

VerwendenDNA (freeze-dried)(pure biological)(pure vegetal)(deoxyribonucleic acid) is a surface film-forming protein with moisturizing action. DnA’s large macromolecules do not enable it to penetrate the skin. In addition, its affinity with the stratum corneum layer keeps it anchored to the skin’s surface, where it serves to protect and retain skin moisture. Although the use of DnA was particularly popular in the 1980s, its incorporation into cosmetic products since then has practically disappeared. It is usually used in a potassium salt form obtained from fish sperm.

Darstellung

synthetischeDeoxyribonucleic acid is synthesized during the division cycle of bacteria and yeast[1-2].

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