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27505

Sigma-Aldrich

D-Citrulline

≥99.0%, for peptide synthesis

Synonym(s):

(R)-2-Amino-5-ureidopentanoic acid

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About This Item

Empirical Formula (Hill Notation):
C6H13N3O3
CAS Number:
Molecular Weight:
175.19
Beilstein:
1725415
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22

product name

D-Citrulline, ≥99.0%

Assay

≥99.0%

form

powder

optical activity

[α]20/D −20.5±2.0°, c = 2% in 1 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

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

InChI

1S/C6H13N3O3/c7-4(5(10)11)2-1-3-9-6(8)12/h4H,1-3,7H2,(H,10,11)(H3,8,9,12)/t4-/m1/s1

InChI key

RHGKLRLOHDJJDR-SCSAIBSYSA-N

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

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Sylvain V Costes et al.
PLoS computational biology, 3(8), e155-e155 (2007-08-07)
Several proteins involved in the response to DNA double strand breaks (DSB) form microscopically visible nuclear domains, or foci, after exposure to ionizing radiation. Radiation-induced foci (RIF) are believed to be located where DNA damage occurs. To test this assumption

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