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16104

Sigma-Aldrich

Sucrose

puriss., meets analytical specification of Ph. Eur., BP, NF

Synonym(s):

α-D-Glc-(1→2)-β-D-Fru, α-D-Glucopyranosyl β-D-fructofuranoside, β-D-Fructofuranosyl-α-D-glucopyranoside, D(+)-Saccharose, Sugar

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About This Item

Empirical Formula (Hill Notation):
C12H22O11
CAS Number:
Molecular Weight:
342.30
Beilstein:
90825
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.21

biological source

plant

Quality Level

Agency

meets analytical specifications of BP
meets analytical specifications of NF
meets analytical specifications of Ph. Eur.

description

color index <= 45

grade

puriss.

form

solid

optical activity

[α]20/D +66.3 to +67.0°, c = 26% in H2O

quality

meets analytical specification of Ph. Eur., BP, NF

impurities

dextrine, complies
invert sugar, complies
organic volatile impurities, in accordance (GC)
reducing sugar, complies
residual solvents, complies
≤0.0005% heavy metals (as Pb)
≤0.0035% Chloride (Cl)
≤0.006% Sulfate (SO4)
≤10 ppm Sulfite (SO2)
≤250 EU/g endotoxins (LAL test)
≤5 ppm Heavy Metals (lead)

ign. residue

≤0.01% (as SO4)

loss

≤0.1% loss on drying, 105 °C, 3 h

color

white

useful pH range

5.5-7 (25 °C, 342 g/L)

conductivity

≤35 μS/cm

mp

185 - 187  °C ((365 - 369 °F ))
185-187 °C (lit.)

solubility

alcohol: soluble 1 gm in 170 ml
methanol: soluble 1 gm in 100ml
H2O: 342 g/L at 20 °C
alcohol: insoluble (Dehydrated)
glycerol: moderately soluble
pyridine: moderately soluble

anion traces

chloride (Cl-): ≤30 mg/kg
sulfate (SO42-): ≤60 mg/kg
sulfite (SO32-): ≤10 mg/kg

cation traces

Ca:, in accordance
Pb: ≤0.5 mg/kg

suitability

complies for appearance of solution

SMILES string

OC[C@H]1O[C@H](O[C@]2(CO)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

application(s)

pharmaceutical (small molecule)

InChI

1S/C12H22O11/c13-1-4-6(16)8(18)9(19)11(21-4)23-12(3-15)10(20)7(17)5(2-14)22-12/h4-11,13-20H,1-3H2/t4-,5-,6-,7-,8+,9-,10+,11-,12+/m1/s1

InChI key

CZMRCDWAGMRECN-UGDNZRGBSA-N

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Application

  • Auxin regulates bulbil initiation by mediating sucrose metabolism in Lilium lancifolium: This study highlights the role of sucrose in regulating the initiation of bulbils in plants, facilitated by auxin signaling, demonstrating its significance in plant developmental processes (Xin et al., 2024).

Biochem/physiol Actions

Sucrose is extracted from cane sugar or beet sugar. It is made up of glucose and fructose and is a good source of carbon and energy. In sugarcane plants, accumulation of sucrose is important in elongation of internodes. Thus metabolism of sucrose plays a major role in the growth of the sugarcane plant.

Other Notes

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Direct microdetermination of sucrose.
E Van Handel
Analytical biochemistry, 22(2), 280-283 (1968-02-01)
Sucrose Metabolism Related to Growth and Ripening in Sugarcane Internodes.
Lingle SE
Crop Science, 31 (1991)
Amorphous state and delayed ice formation in sucrose solutions.
Roos Y and Karel M.
International Journal of Food Science and Technology, 26(6), 553-566 (1991)
U Sonnewald et al.
The Plant journal : for cell and molecular biology, 1(1), 95-106 (1991-07-01)
In higher plants sucrose plays a central roles with respect to both short-term storage and distribution of photoassimilates formed in the leaf. Sucrose is synthesized in the cytosol, transiently stored in the vacuole and exported via the apoplast. In order
Estelle Oberlin et al.
Development (Cambridge, England), 129(17), 4147-4157 (2002-08-07)
Hematopoietic cells arise first in the third week of human ontogeny inside yolk sac developing blood vessels, then, one week later and independently, from the wall of the embryonic aorta and vitelline artery. To address the suggested derivation of emerging

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