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Merck

S7547

D-Sorbit

≥98% (GC), BioXtra

Synonym(e):

D-Glucitol

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250 G

€ 36,80

1 KG

€ 99,50

€ 36,80


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Über diesen Artikel

Empirische Formel (Hill-System):
C6H14O6
CAS-Nummer:
Molekulargewicht:
182.17
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
200-061-5
Beilstein/REAXYS Number:
1721899
MDL number:

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Unterstützung erhalten

SMILES string

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

InChI key

FBPFZTCFMRRESA-JGWLITMVSA-N

InChI

1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5-,6-/m1/s1

vapor density

<1 (vs air)

vapor pressure

<0.1 mmHg ( 25 °C)

product line

BioXtra

assay

≥98% (GC)

form

powder or chunks

impurities

<0.001% Phosphorus (P), <0.1% Insoluble matter

ign. residue

<0.1%

color

white

useful pH range

5.0-7.0 (25 °C, 182 g/L)

mp

98-100 °C (lit.)

solubility

H2O: 1 M, clear, colorless (room temperature)

anion traces

chloride (Cl-): <0.005%, sulfate (SO42-): <0.01%

cation traces

Al: <0.0005%, Ca: <0.0005%, Cu: <0.0005%, Fe: <0.0005%, K: <0.005%, Mg: <0.0005%, NH4+: <0.05%, Na: <0.005%, Pb: <0.001%, Zn: <0.0005%

Quality Level

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Dieser Artikel
S1876S602197336
assay

≥98% (GC)

assay

≥98% (GC)

assay

≥98% (GC)

assay

72-92%

Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

100

solubility

H2O: 1 M, clear, colorless (room temperature)

solubility

water: 200 mg/mL, clear, colorless

solubility

water: soluble 182g/l at 20 °C (68 °F)

solubility

water: soluble 182 g/L at 20 °C (68 °F)

form

powder or chunks

form

powder or crystals

form

powder or crystals

form

liquid

useful pH range

5.0-7.0 (25 °C, 182 g/L)

useful pH range

5.0-7.0 (25 °C, 182 g/L)

useful pH range

5.0-7 (25 °C, 182 g/L)

useful pH range

5.0-7 (25 °C, 182 g/L)

cation traces

Al: <0.0005%, Cu: <0.0005%, K: <0.005%, NH4+: <0.05%, Pb: <0.001%, Ca: <0.0005%, Mg: <0.0005%, Zn: <0.0005%, Fe: <0.0005%, Na: <0.005%

cation traces

-

cation traces

-

cation traces

-

Application

May be used for washing spheroplasts[1] and in isoelectric focusing to minimize endoosmotic flow in agarose gels.[2] May be used to induce osmotic stress.

Biochem/physiol Actions

D-Sorbitol is a sugar alcohol that is commonly used as a sugar substitute. It occurs naturally and is also produced synthetically from glucose. The food industry uses D-sorbitol as an additive in the form of a sweetener, humectant, emulsifier, thickener, or dietary supplement. D-Sorbitol has also been found in cosmetics, paper, and pharmaceuticals. Naturally, D-sorbitol occurs widely in plants via photosynthesis, ranging from algae to higher order fruits of the family Rosaceae.

Other Notes

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

Lagerklasse

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Die Dokumentenbibliothek aufrufen

Isoelectric focusing.
D E Garfin
Methods in enzymology, 182, 459-477 (1990-01-01)
Preparation of extracts from yeast.
S M Jazwinski
Methods in enzymology, 182, 154-174 (1990-01-01)
Arlene E Dent et al.
PloS one, 3(10), e3557-e3557 (2008-10-30)
Antibodies that impair Plasmodium falciparum merozoite invasion and intraerythrocytic development are one of several mechanisms that mediate naturally acquired immunity to malaria. Attempts to correlate anti-malaria antibodies with risk of infection and morbidity have yielded inconsistent results. Growth inhibition assays
J M van Griensven et al.
Clinical pharmacology and therapeutics, 58(6), 631-640 (1995-12-01)
To examine the effect of diabetes mellitus on the pharmacokinetics of tolrestat and to investigate its effect on red blood cell sorbitol levels according to a new pharmacodynamic model for this class of drugs. Single and multiple doses of tolrestat
Anna Boccaccio et al.
Cellular and molecular life sciences : CMLS, 71(21), 4275-4283 (2014-04-29)
Two-pore channel proteins (TPC) encode intracellular ion channels in both animals and plants. In mammalian cells, the two isoforms (TPC1 and TPC2) localize to the endo-lysosomal compartment, whereas the plant TPC1 protein is targeted to the membrane surrounding the large

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