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02240

Adonitol

Name: Adonitol
Brand: SIGMA

BioXtra, ≥99.0% (HPLC)

Synonym(s):

Adonite, Ribitol

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About This Item

Empirical Formula (Hill Notation):

C₅H₁₂O₅

CAS Number:

488-81-3

Molecular Weight:

152.15

NACRES:

NA.25

PubChem Substance ID:

329747403

UNSPSC Code:

12352201

EC Number:

207-685-7

MDL number:

MFCD00064291

Beilstein/REAXYS Number:

1720524

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product line

BioXtra

Quality Level

200

assay

≥99.0% (HPLC)

form

powder

color

colorless

mp

101-105 °C

solubility

water: 1 g/10 mL, clear to slightly hazy, colorless to very faintly yellow

anion traces

chloride (Cl^-): ≤50 mg/kg, sulfate (SO₄^2-): ≤50 mg/kg

cation traces

As: ≤0.1 mg/kg, Ca: ≤50 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤50 mg/kg, K: ≤50 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg

storage temp.

room temp

SMILES string

OC[C@H](O)[C@H](O)[C@H](O)CO

InChI

1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4+,5-

InChI key

HEBKCHPVOIAQTA-ZXFHETKHSA-N

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Related Categories

Biochemicals

Carbohydrates for Biochemical Research

Cell Culture Supplements & Reagents

Chemical Biology

High-Purity Biochemicals and Reagents

General description

Adonitol has similar properties like glycerol and is naturally found in Adonis vernalis.

Adonitol (Ribitol), a pentose alcohol, is metabolized to teicholic acids used in the cell walls of gram positive bacteria. Adonitol is often compared to other cell permeating molecules such as formamide, propanediol, and DMSO as a cryopreservation agent.

Application

Adonitol has been used as an internal standard for the quantification of polyribosyl ribitol phosphate using high pH anion-exchange chromatography with pulsed amperometric detection (HPAEC/PAD).

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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General Organic and Biological Chemistry, An integrated approach (2017)

International collaborative study for establishment of the 2nd WHO International Standard for Haemophilus influenzae type b polysaccharide

Fatme M, et al.

Biologicals : Journal of the International Association of Biological Standardization, 43(6), 492-503 (2015)

Freeze Drying (2004)

Understanding thermodynamic properties at the molecular level: multiple temperature charge density study of ribitol and xylitol.

Anders Østergaard Madsen et al.

The journal of physical chemistry. A, 115(26), 7794-7804 (2011-06-15)

X-ray diffraction data of high quality measured to high resolution on crystals of the two pentitol epimers ribitol (centric) and xylitol (acentric) at 101, 141, and 181 K and data on the two compounds previously recorded at 122 K have

Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols.

Claudia Bello et al.

Bioorganic & medicinal chemistry, 19(24), 7720-7727 (2011-11-15)

New derivatives of 1,4-dideoxy-1,4-imino-D-ribitol have been prepared and evaluated for their cytotoxicity on solid and haematological malignancies. 1,4-Dideoxy-5-O-[(9Z)-octadec-9-en-1-yl]-1,4-imino-D-ribitol (13, IC(50) ∼2 μM) and its C(18)-analogues (IC(50) <10 μM) are cytotoxic toward SKBR3 (breast cancer) cells. 13 also inhibits (IC(50) ∼8

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Global Trade Item Number

SKU	GTIN
8037720250	04022536383231
8037720005	04022536383224
8037721000	04022536383248
W324906-5KG	04061835566808
W324906-1KG	04061835566792
W324906-SAMPLE	04061835566815
1037680100	04022536043975
W324906-10KG	04061834397410
Y0002176	04061841558248
D174904-5G	04061833560624
D175005-500G	04061833560655
D175005-100G	04061833560648
36715-1G	04061831827002
D174904-25G	04061832284095
02240-1G	04061838612281
02240-5G	04061838612304
02240-25G	04061838612298

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