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Merck

8.16014

Sigma-Aldrich

(R)-(+)-Cysteine

for synthesis

Synonym(s):

(R)-(+)-Cysteine, α-Amino-ß-mercapto propionic acid, αlpha-Amino-ß-mercapto propionic acid, Cys, αlpha-Amino-beta-mercapto propionic acid

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25 G
€56.40
100 G
€117.00

About This Item

Empirical Formula (Hill Notation):
C3H7NO2S
CAS Number:
Molecular Weight:
121.16
MDL number:
UNSPSC Code:
12352209
EC Index Number:
200-158-2
NACRES:
NA.22

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€56.40


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Quality Level

form

solid

autoignition temp.

420 °C

potency

1890 mg/kg LD50, oral (Rat)

pH

4.5-5.5 (20 °C, 100 g/L in H2O)

mp

220-228 °C

bulk density

300 kg/m3

storage temp.

2-30°C

SMILES string

SCC([N+H3])C(=O)[O-]

InChI

1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)

InChI key

XUJNEKJLAYXESH-UHFFFAOYSA-N

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This Item
C735295437W326305
L-Cysteine from non-animal source, BioReagent, suitable for cell culture, ≥98%

C7352

L-Cysteine

L-Cysteine certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

95437

L-Cysteine

form

solid

form

crystalline powder

form

-

form

-

storage temp.

2-30°C

storage temp.

-

storage temp.

2-8°C

storage temp.

-

Quality Level

200

Quality Level

200

Quality Level

300

Quality Level

400

mp

220-228 °C

mp

240 °C (dec.) (lit.)

mp

240 °C (dec.) (lit.)

mp

240 °C (dec.) (lit.)

autoignition temp.

420 °C

autoignition temp.

-

autoignition temp.

-

autoignition temp.

-

potency

1890 mg/kg LD50, oral (Rat)

potency

-

potency

-

potency

-

General description

Cysteine is used as a building block in the synthesis of peptides due to its ability to form disulfide bonds. Additionally, it functions as a chiral auxiliary in asymmetric synthesis, facilitating the induction of chirality in the resulting products.

Analysis Note

Assay (HClO₄): ≥ 98.0 %
Spec. rotation [α²0/D (c=8 in HCl 1 mol/l): +8.0 - +9.5 °
Identity (IR): passes test

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1


Certificates of Analysis (COA)

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