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Ampicillin, Anhydrous, 96.0-102.0% (Anh

From £55.13 per (ex VAT)

Ampicillin, Anhydrous, 96.0-102.0% (Anh

Product Code A9393-5G
Unit of Measure 1X5GR
CAS Number 69-53-4
MDL NUMBER MFCD00005175
EMPIRICAL FORMULA C16H19N3O4S
Molecular Weight 349.4
Synonyms D-(-)-Alpha-Aminobenzylpenicillin
Brand SIGMA-ALDRICH

Tiered Pricing - A9393-5G

Qty Discount Price
4+ 13% £62.29
12+ 15% £60.86
36+ 17% £59.43
72+ 23% £55.13
SKU - Pack Size Availability Price (ex VAT) Qty
A9393-25G (1X25GR) Ampicillin, Anhydrous, 96.0-102.0% (Anh Please check stock availability Check Availability £288.00
A9393-5G (1X5GR) Please check stock availability Check Availability £71.60 per EA £71.60
Sub-Total £0.00 (ex VAT)
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Properties

Property Value
eCl@ss 32160000
Shipped on ICE STD
UNSPSC Code 12350000
ADRSuff 1
CAS Number 69-53-4
Storage Temperature 2-8C
EINECSNo 200-709-7
Flash Point Not applicable
GHS Categories Skin Irrit. 2,Skin Sens. 1,Eye Irrit. 2,Resp. Sens. 1,STOT SE 3
GHS Hazard Codes H315-H317-H319-H334-H335
GHS Hazard Statements Causes skin irritation. May cause an allergic skin reaction. Causes serious eye irritation. May cause allergy or asthma symptoms or breathing difficulties if inhaled. May cause respiratory irritation.
GHS Pictograms GHS08,GHS07
GHS Precaution Codes P261 - P280 - P305 + P351 + P338 - P342 + P311
GHS Precaution Statements Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray. Wear protective gloves. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If experiencing respiratory symptoms: Call a PO
GHS Signal Words Danger
Hazard Symbols Xn
Hazard Symbols Descriptions Harmful
MDL Number MFCD00005175
Melting Point 208 C (dec.) (lit.)
Molecular Formula C16H19N3O4S
Molecular Weight 349.4
Net Weight 5
R-Phrases 36/37/38-42/43
RTECSNo XH8350000
S-Phrases 22-26-36/37
Synonyms D-(-)-alpha-Aminobenzylpenicillin
Tariff Number 29411000000
MSDS Link https://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do?country=DElanguage=ENproductNumber=A9393brand=SIGMA
Mode of action cell wall synthesis | interferes
Quality Level 200
storage temp. 2-8C
SMILES string [H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N)c3ccccc3)C(O)=O
form solid
Antibiotic Activity Spectrum Gram-positive bacteria
pKa (25 C) 2.5 (COOH)
InChI key AVKUERGKIZMTKX-NJBDSQKTSA-N
mp 208 C (dec.) (lit.)
InChI 1S/C16H19N3O4S/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23)/t9-,10-,11+,14-/m1/s1
Assay 96.0-102.0% (anhydrous basis)

Description

Ampicillin, Anhydrous, 96.0-102.0% (Anh

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