D-(+)-Arabitol - 10mM in DMSO, high purity , CAS No.488-82-4

2 Citations
  • 10mM in DMSO
Item Number
D424233
Grouped product items
SKUSizeAvailabilityPrice Qty
D424233-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$159.90

Basic Description

SynonymsD-Arabinitol | 488-82-4 | D-Arabitol | DL-Arabitol | arabitol | D-(+)-Arabitol | D-Lyxitol | D-(+)-Arabinitol | arabinitol | Lyxitol | DL-Arabinitol | 2152-56-9 | D-Arabinol | (2R,4R)-pentane-1,2,3,4,5-pentol | 6018-27-5 | (2R,4R)-pentane-1,2,3,4,5-pentaol | D-lyxo-Pentitol | BOA443XF1X | Y
Specifications & Purity10mM in DMSO
Storage TempStore at -80°C
Shipped InIce chest + Ice pads

Associated Targets(Human)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Caenorhabditis elegans (1055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name (2R,4R)-pentane-1,2,3,4,5-pentol
INCHI InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1
InChi Key HEBKCHPVOIAQTA-QWWZWVQMSA-N
Canonical SMILES C(C(C(C(CO)O)O)O)O
Isomeric SMILES C([C@H](C([C@@H](CO)O)O)O)O
WGK Germany 3
PubChem CID 94154
Molecular Weight 152.15
Beilstein 1720520

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

Specific Rotation[α]12° (C=5,Sodium borate(8%))
Melt Point(°C)97-105°C

Safety and Hazards(GHS)

WGK Germany 3
Merck Index 762

Related Documents

Citations of This Product

1. Hengtao Tang, Zhi Chen, Yu Shao, Xin Ju, Liangzhi Li.  (2022)  Development of an enzymatic cascade to systematically utilize lignocellulosic monosaccharide.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  103  (4): (1974-1980).  [PMID:36448581]
2. Xiaolan Li, Yufei Zhang, Hossain M. Zabed, Junhua Yun, Guoyan Zhang, Mei Zhao, Yuvaraj Ravikumar, Xianghui Qi.  (2023)  High-level production of d-arabitol by Zygosaccharomyces rouxii from glucose: Metabolic engineering and process optimization.  BIORESOURCE TECHNOLOGY,  367  (128251).  [PMID:36334865]

References

1. Hengtao Tang, Zhi Chen, Yu Shao, Xin Ju, Liangzhi Li.  (2022)  Development of an enzymatic cascade to systematically utilize lignocellulosic monosaccharide.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  103  (4): (1974-1980).  [PMID:36448581]
2. Xiaolan Li, Yufei Zhang, Hossain M. Zabed, Junhua Yun, Guoyan Zhang, Mei Zhao, Yuvaraj Ravikumar, Xianghui Qi.  (2023)  High-level production of d-arabitol by Zygosaccharomyces rouxii from glucose: Metabolic engineering and process optimization.  BIORESOURCE TECHNOLOGY,  367  (128251).  [PMID:36334865]

Solution Calculators