MilliporeSigma
All Photos(1)

Documents

47627

Sigma-Aldrich

Fmoc-Gly-OH

≥98.0% (T)

Sign Into View Organizational & Contract Pricing

Synonym(s):
Fmoc-glycine
Empirical Formula (Hill Notation):
C17H15NO4
CAS Number:
Molecular Weight:
297.31
Beilstein:
2163967
EC Number:
MDL number:
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

Quality Level

Assay

≥98.0% (T)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

174-175 °C (lit.)
174-178 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)CNC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)

InChI key

NDKDFTQNXLHCGO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
8.5200167041347524
Fmoc-Gly-OH ≥98.0% (T)

Sigma-Aldrich

47627

Fmoc-Gly-OH

Fmoc-Gly-OH Novabiochem®

Sigma-Aldrich

8.52001

Fmoc-Gly-OH

Fmoc-tBu-Gly-OH ≥98.0%

Sigma-Aldrich

47524

Fmoc-tBu-Gly-OH

form

powder

form

powder

form

-

form

solid

mp

174-175 °C (lit.), 174-178 °C

mp

177.4 °C

mp

-

mp

124-127 °C

functional group

Fmoc

functional group

Fmoc

functional group

Boc, Fmoc

functional group

Fmoc, amine, carboxylic acid

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

2-8°C

storage temp.

2-8°C

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

reaction suitability

reaction type: C-H Activation, reaction type: Fmoc solid-phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis

Other Notes

Fmoc-glycine coupling of saccharide β-glycosylamines for the fractionation of oligosaccharides and formation of neoglycoconjugates.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 6

1 of 6

Fmoc-Lys(Boc)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47624

Fmoc-Lys(Boc)-OH

Fmoc-Gln(Trt)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47674

Fmoc-Gln(Trt)-OH

Fmoc-Tyr(tBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47623

Fmoc-Tyr(tBu)-OH

Fmoc-Glu(OtBu)-OH ≥98.0% (HPLC)

Sigma-Aldrich

47625

Fmoc-Glu(OtBu)-OH

Fmoc-Asn(Trt)-OH ≥97.0%

Sigma-Aldrich

47672

Fmoc-Asn(Trt)-OH

Fmoc-His(Trt)-OH ≥98.0% (sum of enantiomers, HPLC)

Sigma-Aldrich

47639

Fmoc-His(Trt)-OH

Jing Fu et al.
Journal of hazardous materials, 368, 186-196 (2019-01-25)
Methyl-triclosan (MTCS), as a biodegradation product from antibacterial triclosan (TCS), has been detected in water catchments, and it has also been verified to accumulate in biota due to its hydrophobicity. There is a lack, however, of toxicity studies on MTCS
Jing Fu et al.
Ecotoxicology and environmental safety, 189, 110039-110039 (2019-12-13)
The omnipresence of antimicrobial triclosan (TCS) and by-products in aquatic environments is a threat to aquatic organisms. Traditionally, the adverse effects of TCS and its by-products have been evaluated by examining the phenotypic output relevant to predicting acute toxicity rather
P H Naccache et al.
Blood, 84(2), 616-624 (1994-07-15)
The control of the adhesive properties of human neutrophils is an essential element of their defense function. One level at which this control is exerted involves the upregulation of the surface expression of beta 2-integrins. In this study, we have
G Arsequell et al.
Analytical biochemistry, 216(1), 165-170 (1994-01-01)
We have devised a new saccharide derivatization scheme to provide not only the temporary attachment of a chromophore for detecting and facilitating the chromatographic separation of carbohydrates, but also the intermediates for further derivatization to produce neoglycoconjugates. Several neutral unprotected
L Noronha-Blob et al.
Gastroenterology, 104(4), 1021-1029 (1993-04-01)
The efficacy of the leukocyte recruitment inhibitor, N-[9H-2,7-dimethylfluoren-9-ylmethoxy)carbonyl]-L-leucine (NPC 15669) was compared with drugs used to treat inflammatory bowel diseases in a rat model, acetic acid-induced colitis. Colonic damage assessed by visual inspection, histological quantitation of tissue injury, vascular permeability

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service