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Key Documents

Outros documentos

I6035

Sigma-Aldrich

L-Iditol

≥98% (GC)

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About This Item

Fórmula empírica (Notação de Hill):
C6H14O6
Número CAS:
488-45-9
Peso molecular:
182.17
Número MDL:
MFCD00064289
Código UNSPSC:
12352201
ID de substância PubChem:
329815389
NACRES:
NA.25

Nível de qualidade

100

Ensaio

≥98% (GC)

forma

solid

cor

white

pf

78-80 °C (lit.)

solubilidade

water: 50 mg/mL, clear, colorless

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

InChI

1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4-,5+,6+/m0/s1

chave InChI

FBPFZTCFMRRESA-UNTFVMJOSA-N

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Descrição geral

A rare sugar alcohol (polyol).

Outras notas

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Diphenhydramine hydrochloride Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1015

Diphenhydramine hydrochloride

D-Psicose ≥95% (HPLC)

Sigma-Aldrich

P8043

D-Psicose

D-(+)-Arabitol ≥99% (GC)

Sigma-Aldrich

A3381

D-(+)-Arabitol

L-(−)-Arabitol ≥98% (GC)

Sigma-Aldrich

A3506

L-(−)-Arabitol

D-Manitol ≥98% (GC)

Sigma-Aldrich

M4125

D-Manitol

Dextromethorphan HBr certified reference material, pharmaceutical secondary standard

Supelco

PHR1018

Dextromethorphan HBr

D-sorbitol ≥98% (GC)

Sigma-Aldrich

S1876

D-sorbitol

D-sorbitol 99% (GC)

Sigma-Aldrich

240850

D-sorbitol

Hexitol anhydrides; 1,4,3,6-dianhydro-L-iditol and the structures of isomannide and isosorbide.
H G FLETCHER et al.
Journal of the American Chemical Society, 68, 939-941 (1946-06-01)
David M Hodgson et al.
Organic letters, 7(12), 2305-2308 (2005-06-04)
[reaction: see text] Reaction of hindered lithium amides with readily available (enantiopure) terminal epoxides gives 2-ene-1,4-diols via carbenoid dimerization of the corresponding alpha-lithiated epoxides. D-Mannitol and D-iditol were synthesized using this method in three steps from (S)-tritylglycidyl ether.
Wojciech Schönemann et al.
Bioorganic & medicinal chemistry, 18(7), 2645-2650 (2010-03-17)
A short synthesis of new beta-1-C-alkyl-1,5-dideoxy-1,5-imino-l-iditols by means of the diastereoselective addition of Grignard reagents onto a glucopyranosylamine is described. These compounds were evaluated as beta-glucocerebrosidase inhibitors and their activity was compared with that of related iminosugar derivatives in the
N A Williams et al.
Journal of parenteral science and technology : a publication of the Parenteral Drug Association, 47(3), 119-123 (1993-05-01)
The mechanical properties of frozen mannitol, L-iditol, dulcitol, and sorbitol solutions were measured as a function of temperature during warming (after freezing) using a thermal mechanical analyzer (TMA). The mannitol sample first underwent a contractive phase starting at 30 degrees
C A Brearley et al.
The Biochemical journal, 314 ( Pt 1), 215-225 (1996-02-15)
We have undertaken an analysis of the inositol phosphates of Spirodela polyrhiza at a developmental stage when massive accumulation of InsP6 indicates that a large net synthesis is occurring. We have identified Ins3P, Ins(1,4)P2, Ins(3,4)P2 and possibly Ins(4,6)P2, Ins(3,4,6)P3, Ins(3,4,5,6)P4
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