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Merck

A5665

Sigma-Aldrich

Adenina

BioReagent, suitable for plant cell culture, ≥99%

Sinónimos:

6-Aminopurina, Vitamina B4

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About This Item

Fórmula empírica (notación de Hill):
C5H5N5
Número de CAS:
Peso molecular:
135.13
Beilstein/REAXYS Number:
5777
EC Number:
MDL number:
UNSPSC Code:
10171502
PubChem Substance ID:
NACRES:
NA.72

product line

BioReagent

assay

≥99%

form

powder

mol wt

Mw 135.13 g/mol

technique(s)

cell culture | plant: suitable

color

white to off-white

mp

>360 °C (lit.)

solubility

0.5 M HCl: soluble 20 mg/mL, clear to slightly hazy, colorless to faintly yellow

application(s)

agriculture

SMILES string

Nc1ncnc2[nH]cnc12

InChI

1S/C5H5N5/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H3,6,7,8,9,10)

InChI key

GFFGJBXGBJISGV-UHFFFAOYSA-N

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General description

Adenine (Ade) is a purine base, which is present in nucleic acids. It binds with ribose to form nucleoside adenosine (A) and attach to deoxyribose to form nucleoside deoxyadenosine (dA).

Application

Adenine has been used in yeast extract supplemented (YES) broth and yeast nitrogen base glutamate (YNG)l media.
Adenine may be used as a plant cell culture additive. Adenine Sulphate (25mg/L) in the culture media such as Murashige & Skoog media improves the frequency of multiple shoot production and recovered the chlorotic symptoms of the leaves.

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificados de análisis (COA)

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Single-step marker switching in Schizosaccharomyces pombe using a lithium acetate transformation protocol
Brown S D and Lorenz A
Bio-protocol, 6(24) (2016)
Adenine
Encyclopedia of Genetics (2001)
Didier Wion et al.
Nature reviews. Microbiology, 4(3), 183-192 (2006-02-21)
N(6)-methyl-adenine is found in the genomes of bacteria, archaea, protists and fungi. Most bacterial DNA adenine methyltransferases are part of restriction-modification systems. Certain groups of Proteobacteria also harbour solitary DNA adenine methyltransferases that provide signals for DNA-protein interactions. In gamma-proteobacteria
Georg Behrens et al.
AIDS patient care and STDs, 28(4), 168-175 (2014-03-26)
The once daily, single-tablet regimen (STR) combining rilpivirine (RPV), emtricitabine (FTC), and tenofovir disoproxil fumarate (TDF) provides a simplified treatment option for antiretroviral therapy (ART)-naïve patients with baseline HIV-1 RNA (BLVL) of ≤100,000 copies/mL. The aim of this analysis is
Jennifer B Kozdon et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(48), E4658-E4667 (2013-11-13)
The Caulobacter DNA methyltransferase CcrM is one of five master cell-cycle regulators. CcrM is transiently present near the end of DNA replication when it rapidly methylates the adenine in hemimethylated GANTC sequences. The timing of transcription of two master regulator

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