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MilliporeSigma

P5960

L-Pyroglutamic acid

≥97% (titration), suitable for plant cell culture, BioXtra

Synonym(s):

(S)-(−)-2-Pyrrolidone-5-carboxylic acid, (S)-5-Oxo-2-pyrrolidinecarboxylic acid

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25 G

$86.00

$86.00

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About This Item

Empirical Formula (Hill Notation):
C5H7NO3
CAS Number:
98-79-3
Molecular Weight:
129.11
NACRES:
NA.26
PubChem Substance ID:
24898722
UNSPSC Code:
12352209
EC Number:
202-700-3
MDL number:
MFCD00005272
Beilstein/REAXYS Number:
82132

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Product Name

L-Pyroglutamic acid, BioXtra

InChI

1S/C5H7NO3/c7-4-2-1-3(6-4)5(8)9/h3H,1-2H2,(H,6,7)(H,8,9)/t3-/m0/s1

InChI key

ODHCTXKNWHHXJC-VKHMYHEASA-N

SMILES string

OC(=O)[C@@H]1CCC(=O)N1

product line

BioXtra

assay

≥97% (titration)

form

powder

technique(s)

cell culture | plant: suitable

impurities

≤0.0005% Phosphorus (P)

ign. residue

≤0.1%

color

white

mp

160-163 °C (lit.)

solubility

H2O: 1 M, clear, colorless

anion traces

chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%

cation traces

Al: ≤0.0005%
Ca: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.005%
Pb: ≤0.001%
Zn: ≤0.0005%

Quality Level

200

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1 of 4

This Item
Y000012383160PHR2817
L-Pyroglutamic acid BioXtra

Sigma-Aldrich

P5960

L-Pyroglutamic acid

Pidolic acid European Pharmacopoeia (EP) Reference Standard

Y0000123

Pidolic acid

L-Pyroglutamic acid ≥99.0% (T)

Sigma-Aldrich

83160

L-Pyroglutamic acid

Pyroglutamic Acid Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR2817

Pyroglutamic Acid

form

powder

form

-

form

solid

form

solid

assay

≥97% (titration)

assay

-

assay

≥99.0% (T)

assay

-

technique(s)

cell culture | plant: suitable

technique(s)

-

technique(s)

-

technique(s)

-

product line

BioXtra

product line

-

product line

-

product line

-

cation traces

Al: ≤0.0005%, Cu: ≤0.0005%, K: ≤0.005%, NH4+: ≤0.05%, Pb: ≤0.001%, Ca: ≤0.0005%, Mg: ≤0.0005%, Zn: ≤0.0005%, Fe: ≤0.0005%, Na: ≤0.005%

cation traces

-

cation traces

-

cation traces

-

impurities

≤0.0005% Phosphorus (P)

impurities

-

impurities

-

impurities

-

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000484364
0000484364
0000484363
0000484363
0000369813

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Li-Hui Sun et al.
Chemical communications (Cambridge, England), 47(36), 10136-10138 (2011-08-11)
The chiral N-heterocyclic carbene bearing a proximal hydroxy group derived from L-pyroglutamic acid was found to be an efficient catalyst for the [3+2] annulation of enals and isatins to give the corresponding spirocyclic oxindolo-γ-butyrolactones in good yield with good diastereo-
Franz Gruber et al.
Current biology : CB, 23(6), 507-514 (2013-03-13)
Motivation controls behavior [1]. A variety of food-related behaviors undergo motivational modulation by hunger, satiety, and other states [2-4]. Here we searched for critical satiation factors modulating approach to an odor associated with sugar reward in Drosophila melanogaster. We selectively
P J Caspers et al.
The Journal of investigative dermatology, 116(3), 434-442 (2001-03-07)
Confocal Raman spectroscopy is introduced as a noninvasive in vivo optical method to measure molecular concentration profiles in the skin. It is shown how it can be applied to determine the water concentration in the stratum corneum as a function
Andrea Bednářová et al.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 164(1), 91-100 (2012-10-23)
Glucagon is conventionally regarded as a hormone, counter regulatory in function to insulin and plays a critical anti-hypoglycemic role by maintaining glucose homeostasis in both animals and humans. Glucagon performs this function by increasing hepatic glucose output to the blood
M H Creer et al.
Clinical chemistry, 35(4), 684-686 (1989-04-01)
Pyroglutamic acidemia, a rare metabolic disorder, usually appears in infancy. It is characterized by retardation, ataxia, hemolytic anemia, and chronic acidosis and is caused by a marked deficiency of glutathione synthetase (EC 6.3.2.3) activity. This disease is inherited as an
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