C5269

Clindamycin hydrochloride

lincosamide antibiotic

Manufacturer: Sigma Aldrich

CAS Number: 21462-39-5

Synonym(S): (7S)-7-Chloro-7-deoxylincomycin hydrochloride, Cleocin

Select a Size

Pack Size SKU Availability Price
10 MG C5269-10-MG In Stock ₹ 10,722.60
50 MG C5269-50-MG In Stock ₹ 25,707.60
100 MG C5269-100-MG In Stock ₹ 40,914.60

C5269 - 10 MG

₹ 10,722.60

In Stock

Quantity

1

Base Price: ₹ 10,722.60

GST (18%): ₹ 1,930.068

Total Price: ₹ 12,652.668

Quality Level

200

form

crystalline

impurities

≤2 mol/mol EtOH

solubility

H2O: 50 mg/mL

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

Mode of action

protein synthesis | interferes

storage temp.

2-8°C

SMILES string

Cl.CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)C2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O

InChI

1S/C18H33ClN2O5S.ClH/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4;/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25);1H/t9-,10+,11-,12+,13-,14+,15+,16+,18+;/m0./s1

InChI key

AUODDLQVRAJAJM-XJQDNNTCSA-N

Other Options

Image Product Name Manufacturer Price Range
C2250000
Clindamycin hydrochloride
Sigma Aldrich ₹ 20,567.50

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Description

  • General description: Chemical structure: macrolide
  • Application: Clindamycin is used to study bacterial infections, such as group B streptococcal disease, bacterial resistance and plasma protein binding.[1][2][3]
  • Biochem/physiol Actions: Clindamycin hydrochloride is highly effective against anaerobic species.[4]
  • Other Notes: Antibacterial and antiprotozoal antibiotic of the lincosamide class.

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H317,H319,H362

Precautionary Statements

P260 - P263 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Eye Irrit. 2 - Lact. - Skin Sens. 1

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Compare Similar Items

Show Difference

Img

Sigma Aldrich

C5269

lincosamide antibiotic...


Quality Level:
200

form:
crystalline

impurities:
≤2 mol/mol EtOH

solubility:
H2O: 50 mg/mL

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria

Mode of action:
protein synthesis | interferes

storage temp.:
2-8°C

SMILES string:
Cl.CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)C2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O

InChI:
1S/C18H33ClN2O5S.ClH/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4;/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25);1H/t9-,10+,11-,12+,13-,14+,15+,16+,18+;/m0./s1

InChI key:
AUODDLQVRAJAJM-XJQDNNTCSA-N

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crystalline powder

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

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