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33226

Sigma-Aldrich

Glycine

puriss. p.a., reag. Ph. Eur., buffer substance, 99.7-101% (calc. to the dried substance)

Synonym(s):

Aminoacetic acid, Aminoethanoic acid, Glycocoll

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25 G
¥2,465.37
500 G
¥10,505.95

¥2,465.37

Available to ship on2025年4月27日Details

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25 G
¥2,465.37
500 G
¥10,505.95

About This Item

Linear Formula:
NH2CH2COOH
CAS Number:
56-40-6
Molecular Weight:
75.07
Beilstein:
635782
EC Number:
200-272-2
MDL number:
MFCD00008131
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57648780
NACRES:
NA.21

¥2,465.37

Available to ship on2025年4月27日Details

Request a Bulk Order

Agency

USP/NF
reag. Ph. Eur.

Quality Level

200

grade

puriss. p.a.

Assay

99.7-101% (calc. to the dried substance)

form

crystalline powder

technique(s)

IR spectroscopy: suitable

impurities

≤0.001% heavy metals (as Pb)
≤0.02% ammonium (NH4)
≤0.1% water (Karl Fischer)
≤1.0% ninhydrin-positive substances

ign. residue

≤0.05% (as SO4)

loss

≤0.5% loss on drying, 105°C, 2 h

pH

5.9-6.4 (20 °C, 5%)

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This Item
D15292780352513259
Dimethyl carbonate battery grade, ≥99.9%, acid <10 ppm, H2O <10 ppm

809942

Dimethyl carbonate

Dimethyl carbonate ReagentPlus®, 99%

D152927

Dimethyl carbonate

Dimethyl carbonate for synthesis

803525

Dimethyl carbonate

Dimethyl carbonate analytical standard

13259

Dimethyl carbonate

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

grade

battery grade

grade

-

grade

-

grade

analytical standard

form

liquid

form

liquid

form

liquid

form

-

application(s)

battery manufacturing

application(s)

-

application(s)

-

application(s)

environmental
pharmaceutical

impurities

≤10 ppm H2O, ≤10 ppm acid

impurities

-

impurities

-

impurities

≤0.02% water

assay

≥99.9%

assay

99%

assay

≥99.0% (GC)

assay

≥99.0% (GC)

Application

Glycine can be used as:
  • A reactant in the natural soil clay-catalyzed cleavage and polycondensation with pyrogallol.
  • A catalyst in the Knoevenagel reaction between aryl aldehydes and malononitrile to form a C=C bond.
  • A reagent in the metal-free synthesis of biaryls from aryl sulfoxides and sulfonanilides via sigmatropic rearrangement.

Biochem/physiol Actions

Inhibitory neurotransmitter in spinal cord, allosteric regulator of NMDA receptors.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
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    Certificates of Analysis (COA)

    Lot/Batch Number
    SDBB2364
    SDBB2230
    STBL3196
    STBH1301
    STBL1005

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    Richard A Felix et al.
    Brain structure & function, 220(5), 2639-2652 (2014-06-30)
    The mammalian superior paraolivary nucleus (SPON) is a major source of GABAergic inhibition to neurons in the inferior colliculus (IC), a well-studied midbrain nucleus that is the site of convergence and integration for the majority ascending auditory pathways en route
    Alexander Carvajal-González et al.
    Brain : a journal of neurology, 137(Pt 8), 2178-2192 (2014-06-22)
    The clinical associations of glycine receptor antibodies have not yet been described fully. We identified prospectively 52 antibody-positive patients and collated their clinical features, investigations and immunotherapy responses. Serum glycine receptor antibody endpoint titres ranged from 1:20 to 1:60 000.
    Li-Chun Tu et al.
    The EMBO journal, 32(24), 3220-3230 (2013-11-12)
    Nuclear pore complexes (NPCs) mediate cargo traffic between the nucleus and the cytoplasm of eukaryotic cells. Nuclear transport receptors (NTRs) carry cargos through NPCs by transiently binding to phenylalanine-glycine (FG) repeats on intrinsically disordered polypeptides decorating the NPCs. Major impediments
    Suzanne L Grant et al.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 844(2), 278-282 (2006-08-08)
    A simple and versatile methodology using high-performance liquid chromatography (HPLC) with fluorimetric detection was developed to simultaneously determine d-serine along with other metabolically related neuroactive amino acids in the glutamatergic system: L-serine, L-glutamate, L-glutamine, and glycine. On-column sensitivity was in
    Zoé Husson et al.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 34(28), 9418-9431 (2014-07-11)
    The principal neurons of the cerebellar nuclei (CN), the sole output of the olivo-cerebellar system, receive a massive inhibitory input from Purkinje cells (PCs) of the cerebellar cortex. Morphological evidence suggests that CN principal cells are also contacted by inhibitory
    View All Related Papers

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