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Merck
CN

10850

D-(-)-阿拉伯糖

suitable for microbiology, ≥99.0%

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关于此项目

经验公式(希尔记法):
C5H10O5
化学文摘社编号:
分子量:
150.13
UNSPSC Code:
41106212
NACRES:
NA.85
PubChem Substance ID:
EC Number:
233-708-5
Beilstein/REAXYS Number:
1723079
MDL number:
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Quality Level

assay

≥99.0% (sum of enantiomers, HPLC), ≥99.0%

form

powder

optical activity

[α]20/D −104±2.0°, 24 hr, c = 10% in H2O

ign. residue

≤0.1% (as SO4)

loss

≤0.1% loss on drying, 20 °C (HV)

mp

162-164 °C (lit.)

anion traces

chloride (Cl-): ≤50 mg/kg, sulfate (SO42-): ≤50 mg/kg

cation traces

As: ≤0.1 mg/kg, Ca: ≤500 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤25 mg/kg, Fe: ≤17 mg/kg, K: ≤50 mg/kg, Mg: ≤10 mg/kg, Mn: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Zn: ≤15 mg/kg

application(s)

microbiology

SMILES string

O[C@@H]1COC(O)[C@@H](O)[C@@H]1O

InChI

1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3-,4+,5?/m1/s1

InChI key

SRBFZHDQGSBBOR-ZRMNMSDTSA-N

General description

D-Arabinose is a rare aldopentose, and is rarely utilized by enteric bacteria as a source of carbon and energy. It is also found in the aloins of the plant genus Aloe and as a constituent of the polysaccharide of the bacterial genus Mycobacterium. Some of the enteric bacteria like Escherichia coli K-12 can mutate to utilize D-arabinose.

Application

D-(-)-Arabinose has been used as an inducer of λ-RED recombinant gene expression.

Biochem/physiol Actions

D-阿拉伯糖是一种还原糖。它是一种 D-核糖的戊糖类似物,是组成分支杆菌细胞壁阿拉伯半乳聚糖的成分。也是酵母中 D-红抗坏血酸合成的底物。


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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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商品

Culture media provides a habitat with suitable nutrients, energy sources, and certain environmental conditions for the growth of microorganisms. The components of the culture media range from simple sugars to peptones, salts, antibiotics, and complex indicators.


The Evolution of Metabolic Function.
Mortlock RP.
Science, 16-17 (1992)
A Hasegawa et al.
Carbohydrate research, 52, 137-149 (1976-12-01)
Prumycin (1) and related compounds have been synthesized from benzyl 2-(benzyloxycarbonyl)amino-2-deoxy-5,6-O-isopropylidene-beta-D-glucofuranoside (4). Benzoylation of 4, followed by deisopropylidenation, gave benzyl 3-O-benzoyl-2-(benzyloxycarbonyl)amino-2-deoxy-beta-D-glucofuranoside (6), which was converted, via oxidative cleavage at C-5-C-6 and subsequent reduction, into the related benzyl beta-D-xylofuranoside derivative (7).
Engineering complex biological systems in bacteria through recombinase-assisted genome engineering.
Santos CN and Yoshikuni Y2
Nature Protocols, 9, 1320-1336 (2014)



全球贸易项目编号

货号GTIN
10850-100G04061838686114
10850-25G04061838686121