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A91906

Sigma-Aldrich

L-(+)-Arabinose

98%

Synonym(s):

(+)-Arabinose

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100 μG
CA$620.00

CA$620.00


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100 μG
CA$620.00

About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
Beilstein/REAXYS Number:
1723085
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.22

CA$620.00


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Quality Level

assay

98%

form

powder

optical activity

[α]20/D +103°, c = 1 in H2O

mp

160-163 °C (lit.)

SMILES string

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

InChI

1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m0/s1

InChI key

PYMYPHUHKUWMLA-VAYJURFESA-N

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This Item
Z370762Z131121Z720445
material

polypropylene

material

polypropylene

material

polypropylene

material

polymethylpentene

volume measuring range

2000 mL

volume measuring range

1000 mL

volume measuring range

1000 mL, accuracy: 5.0 mL

volume measuring range

2000 mL, accuracy: 12.0 mL

manufacturer/tradename

Bel-Art F28461-2000

manufacturer/tradename

Bel-Art F28461-1000

manufacturer/tradename

Nalgene 3662-1000

manufacturer/tradename

Nalgene 3663-2000

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea, case of 6 ea

packaging

pack of 1 ea, case of 4 ea

Application

L-(+)-Arabinose is used as a key starting material in the total synthesis of (+)-ambruticin, zaragozic acid A, (−)-radicamine B and (+)-herbarumin I.[1][2][3][4]

Biochem/physiol Actions

L-Arabinose is the naturally occurring isomer and is a constituent of plant polysaccharides. Most bacteria contain an inducible arabinose operon that codes for a series of enzymes and transporters that allows L-arabinose to be used as the sole carbon source in microbial culture.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

Eyeshields, Gloves, type N95 (US)


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