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L254

Sigma-Aldrich

D-Lactose monohydrate

ACS reagent

Synonyme(s) :

β-D-Gal-(1→4)-D-Glc, 4-O-β-D-Galactopyranosyl-D-glucose, Sucre de lait

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About This Item

Formule empirique (notation de Hill):
C12H22O11 · H2O
Numéro CAS:
64044-51-5
Poids moléculaire :
360.31
Numéro Beilstein :
3768231
Numéro CE :
200-559-2
Numéro MDL:
MFCD00166994
Code UNSPSC :
12352100
ID de substance PubChem :
329817398
Nomenclature NACRES :
NA.21

Qualité

ACS reagent

Niveau de qualité

200

Forme

powder

Activité optique

[α]22/D +52.4°, c = 4.5 in H2O

Impuretés

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

Résidus de calcination

≤0.03%

Pf

219 °C (dec.)

Traces de cations

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

Chaîne SMILES 

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

Clé InChI

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).

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
MKCW2072
MKCW2073
MKCV7096
MKCT1114
MKCV0664

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Daniel Cavanagh et al.
Applied and environmental microbiology, 81(12), 3961-3972 (2015-04-05)
Lactococcus lactis is predominantly associated with dairy fermentations, but evidence suggests that the domesticated organism originated from a plant niche. L. lactis possesses an unusual taxonomic structure whereby strain phenotypes and genotypes often do not correlate, which in turn has
Akhtar Siddiqui et al.
Journal of pharmaceutical sciences, 103(9), 2819-2828 (2014-03-04)
The objective of this study was to develop powder X-ray diffraction (XRPD) chemometric model for quantifying crystalline tacrolimus from solid dispersion (SD). Three SDs (amorphous tacrolimus component) with varying drug to excipient ratios (24.4%, 6.7%, and 4.3% drug) were prepared.
J Nijdam et al.
Colloids and surfaces. B, Biointerfaces, 123, 53-60 (2014-09-30)
Segregation of the protein bovine serum albumin (BSA) and lactose in thin aqueous films during drying was investigated by examining the composition of the dried films using inverse micro Raman spectroscopy (IMRS) and X-ray photoelectron spectroscopy (XPS) sputter-depth profiling. The
Fan Zhou et al.
Scientific reports, 1, 78-78 (2012-02-23)
The invisibility cloak has been a long-standing dream for many researchers over the decades. Using transformation optics, a three-dimensional (3D) object is perceived as having a reduced number of dimensions, making it "undetectable" judging from the scattered field12345. Despite successful
Akhtar Siddiqui et al.
International journal of pharmaceutics, 493(1-2), 1-6 (2015-07-26)
The objective of this study was to develop and validate XRPD analytical method for the estimation of percent crystalline warfarin sodium present in drug products. Warfarin sodium (WS) is a clathrate containing Isopropyl alcohol entrapped in the crystalline structure. Four
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