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Key Documents

L254

Sigma-Aldrich

D-Lactose monohydrate

ACS reagent

Synonym(s):

β-D-Gal-(1→4)-D-Glc, 4-O-β-D-Galactopyranosyl-D-glucose, Milk sugar

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About This Item

Empirical Formula (Hill Notation):
C12H22O11 · H2O
CAS Number:
Molecular Weight:
360.31
Beilstein/REAXYS Number:
3768231
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

form

powder

optical activity

[α]22/D +52.4°, c = 4.5 in H2O

impurities

dextrose, passes test
sucrose, passes test
≤0.005% insolubles
4.0-6.0% water

ign. residue

≤0.03%

mp

219 °C (dec.)

cation traces

Fe: ≤5 ppm
heavy metals: ≤5 ppm (by ICP)

functional group

aldehyde
ether

SMILES string

O.OC[C@@H](O)[C@@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@@H](O)C=O

InChI

1S/C12H22O11.H2O/c13-1-4(16)7(18)11(5(17)2-14)23-12-10(21)9(20)8(19)6(3-15)22-12;/h1,4-12,14-21H,2-3H2;1H2/t4-,5+,6+,7+,8-,9-,10+,11+,12-;/m0./s1

InChI key

HBDJFVFTHLOSDW-XBLONOLSSA-N

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Application

  • Synthesis of lactose-based surfactants: Research by Enayati, Gong, and Abbaspourrad demonstrated the use of d-Lactose monohydrate in the synthesis of lactose lauryl ester, employing aluminosilicate zeolite as a catalyst. This study presents a method for producing non-ionic surfactants, highlighting d-Lactose monohydrate′s role in industrial and pharmaceutical applications (Enayati et al., 2019).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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