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Merck
모든 사진(3)

주요 문서

116122

Sigma-Aldrich

D-2-Aminobutyric acid

98%

동의어(들):

(R)-(−)-2-Aminobutyric acid

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About This Item

Linear Formula:
C2H5CH(NH2)CO2H
CAS Number:
Molecular Weight:
103.12
Beilstein:
1720934
EC Number:
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

양식

solid

광학 활성

[α]20/D −21 to −19°, c = 4 in H2O

광학 순도

ee: 98% (GLC)

반응 적합성

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

응용 분야

peptide synthesis

SMILES string

CC[C@@H](N)C(O)=O

InChI

1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m1/s1

InChI key

QWCKQJZIFLGMSD-GSVOUGTGSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Chen Qi et al.
Polymers, 12(9) (2020-09-13)
Eight kinds of chiral diacid monomers were prepared with amino acids with different side groups or configurations. Polyester-imides (PEIs) were synthesized from these diacid monomers and diphenol monomers through polycondensation reaction, and the performances and properties were compared with the
Zhiying Wang et al.
Communications biology, 3(1), 39-39 (2020-01-24)
Osteoporosis is a highly prevalent chronic aging-related disease that frequently is only detected after fracture. We hypothesized that aminobutyric acids could serve as biomarkers for osteoporosis. We developed a quick, accurate, and sensitive screening method for aminobutyric acid isomers and
Jong Jin Lee et al.
Nuclear medicine and biology, 39(3), 325-333 (2011-12-06)
We evaluated new (111)In-labeled amino acid derivatives, in which the amino acids are conjugated with1,4,7,10-tetra-azacyclododecane-1,4,7,10-tetraacetic acid (DOTA), 1,4,7,10-tetraazacyclododecane-1,7-diacetic acid (DO2A) or 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DO3A). DOTA-aminoalanine (DOTA-A), DOTA-aminohomoalanine (DOTA-H), DOTA-lysine (DOTA-L), DO2A-alanine (DO2A-A), DO3A-alanine (DO3A-A) and DO3A-homoalanine (DO3A-H) were labeled with
Site-selective traceless Staudinger ligation for glycoprotein synthesis reveals scope and limitations.
Gonçalo J L Bernardes et al.
Chembiochem : a European journal of chemical biology, 12(9), 1383-1386 (2011-05-21)
Francesco Gasparrini et al.
Journal of the American Chemical Society, 130(2), 522-534 (2007-12-22)
The structure, stability, and reactivity of proton-bound diastereomeric [M x H x A]+ complexes between some amino acid derivatives (A) and several chiral tetra-amide macrocycles (M) have been investigated in the gas phase by ESI-FT-ICR and ESI-ITMS-CID mass spectrometry. The

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