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V-015

Supelco

(−)-Riboflavina

100 μg/mL (Methanol:0.1% Ammonium acetate in Water (1:1)), ampule of 1 mL, analytical standard, Cerilliant®

Sinonimo/i:

Lattoflavina, Vitamina B2, Vitamina G

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About This Item

Formula empirica (notazione di Hill):
C17H20N4O6
Numero CAS:
83-88-5
Peso molecolare:
376.36
Beilstein:
97825
Numero MDL:
MFCD00005022
Codice UNSPSC:
41116107
ID PubChem:
329828958

Grado

analytical standard
certified reference material

Livello qualitativo

100

Forma fisica

liquid

Caratteristiche

Snap-N-Spike®/Snap-N-Shoot®

Confezionamento

ampule of 1 mL

Produttore/marchio commerciale

Cerilliant®

Concentrazione

100 μg/mL (Methanol:0.1% Ammonium acetate in Water (1:1))

Punto di fusione

290 °C (dec.) (lit.)

applicazioni

clinical testing

Formato

single component solution

Temperatura di conservazione

2-8°C

Stringa SMILE

CC1=C(C)C=C(N(C[C@H](O)[C@@H]([C@H](O)CO)O)C(C2=N3)=NC(NC2=O)=O)C3=C1

InChI

1S/C17H20N4O6/c1-7-3-9-10(4-8(7)2)21(5-11(23)14(25)12(24)6-22)15-13(18-9)16(26)20-17(27)19-15/h3-4,11-12,14,22-25H,5-6H2,1-2H3,(H,20,26,27)/t11-,12+,14-/m0/s1
AUNGANRZJHBGPY-SCRDCRAPSA-N

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Note legali

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

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Avvertenze

Danger

Indicazioni di pericolo

H225,H301 + H311 + H331,H370

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Organi bersaglio

Eyes

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

49.5 °F - closed cup

Punto d’infiammabilità (°C)

9.7 °C - closed cup

Certificati d'analisi (COA)

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(−)-Riboflavina United States Pharmacopeia (USP) Reference Standard

USP

1603006

(−)-Riboflavina

(−)-Riboflavina European Pharmacopoeia (EP) Reference Standard

R0600000

(−)-Riboflavina

(−)-Riboflavina meets USP testing specifications

Sigma-Aldrich

R7649

(−)-Riboflavina

Folic acid ≥97%

Sigma-Aldrich

F7876

Folic acid

Madina Mansurova et al.
Chembiochem : a European journal of chemical biology, 14(5), 645-654 (2013-03-05)
Two chemically synthesized flavin derivatives, 8-trifluoromethyl- and 8-bromoriboflavin (8-CF(3)RF and 8-BrRF), were photochemically characterized in H(2)O and studied spectroscopically after incorporation into the LOV domain of the blue light photoreceptor YtvA from Bacillus subtilis. The spectroscopic studies were paralleled by
Caroline Butler et al.
The Cochrane database of systematic reviews, 3(3), CD009072-CD009072 (2013-04-02)
Platelet transfusions are used to prevent and treat bleeding in patients who are thrombocytopenic. Despite improvements in donor screening and laboratory testing, a small risk of viral, bacterial or protozoal contamination of platelets remains. There is also an ongoing risk
Simone Langer et al.
Biochemistry, 52(25), 4288-4295 (2013-05-30)
The Gram-positive bacterium Streptomyces davawensis is the only organism known to produce the antibiotic roseoflavin. Roseoflavin is a structural riboflavin analogue and is converted to the flavin mononucleotide (FMN) analogue roseoflavin mononucleotide (RoFMN) by flavokinase. FMN-dependent homodimeric azobenzene reductase (AzoR)
David T C Lin et al.
Journal of refractive surgery (Thorofare, N.J. : 1995), 28(11 Suppl), S841-S848 (2013-03-02)
To report results of a series of highly aberrated corneas treated with a topography-guided excimer laser ablation. Retrospective, nonrandomized, consecutive series of eyes treated with topography-guided photorefractive keratectomy (TG-PRK) with the customized topographical neutralization technique (TNT). Cases included postoperative refractive
Ambreen Hafeez et al.
Pakistan journal of pharmaceutical sciences, 26(3), 487-493 (2013-04-30)
Riboflavin (vitamin B2) belongs to a group of respiratory enzymes that occur widely in animals and plants participating in vital oxidation- reduction processes in the body. A computational study was conducted on riboflavin by ArgusLab 4.0.1 to obtain the most
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